- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05466604
Comparison of Hyaluronidase and Dexametasone in Reduction of Postoperative Edema
July 15, 2022 updated by: Onur Koç, Hacettepe University
Comparison of the Effects of Hyaluronidase and Dexamethasone on Reduction of Postoperative Edema in Impacted Wisdom Teeth Surgery
The present study is designed to reveal effectiveness of hyaluronidase and dexamethasone on reduction of postoperative edema, pain, trismus, and infection.
For this purpose, 60 participants with symmetrical mandibular wisdom teeth enrolled the present study.
All measurements and evaluations were performed before and 1, 2, 3, and 7 days later the operation.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
60
Phase
- Phase 4
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- symmetrical mandibular wisdom teeth with bone retention
- patients who are signed informed consent and acceptance of study involvement forms
Exclusion Criteria:
- existence of any systemic disease
- existence of any periodical drug intake
- existence of difference in operation times of right and left impacted wisdom teeth extractions more than 5 minutes
- existence of pregnancy
- existence of breastfeeding
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: hyaluronidase
|
injection of 150 IU hyaluronidase to perioperative region, submucosally.
|
|
No Intervention: hyaluronidase control
|
|
|
Experimental: dexamethasone
|
injection of 8 mg dexamethasone to perioperative region, submucosally.
|
|
No Intervention: dexamethasone control
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
evaluation of the increase of edema in postoperative 1. day using a measuring tape in hyaluronidase experimental group
Time Frame: postoperative 1. day
|
preoperative edema amount was subtracted from edema amount in 1. day in hyaluronidase experimental group
|
postoperative 1. day
|
|
evaluation of the increase of edema in postoperative 2. day using a measuring tape in hyaluronidase experimental group
Time Frame: postoperative 2. day
|
preoperative edema amount was subtracted from edema amount in 2. day in hyaluronidase experimental group
|
postoperative 2. day
|
|
evaluation of the increase of edema in postoperative 3. day using a measuring tape in hyaluronidase experimental group
Time Frame: postoperative 3. day
|
preoperative edema amount was subtracted from edema amount in 3. day in hyaluronidase experimental group
|
postoperative 3. day
|
|
evaluation of the increase of edema in postoperative 7. day using a measuring tape in hyaluronidase experimental group
Time Frame: postoperative 7. day
|
preoperative edema amount was subtracted from edema amount in 7. day in hyaluronidase experimental group
|
postoperative 7. day
|
|
evaluation of the increase of edema in postoperative 1. day using a measuring tape in hyaluronidase control group
Time Frame: postoperative 1. day
|
preoperative edema amount was subtracted from edema amount in 1. day in hyaluronidase control group
|
postoperative 1. day
|
|
evaluation of the increase of edema in postoperative 2. day using a measuring tape in hyaluronidase control group
Time Frame: postoperative 2. day
|
preoperative edema amount was subtracted from edema amount in 2. day in hyaluronidase control group
|
postoperative 2. day
|
|
evaluation of the increase of edema in postoperative 3. day using a measuring tape in hyaluronidase control group
Time Frame: postoperative 3. day
|
preoperative edema amount was subtracted from edema amount in 3. day in hyaluronidase control group
|
postoperative 3. day
|
|
evaluation of the increase of edema in postoperative 7. day using a measuring tape in hyaluronidase control group
Time Frame: postoperative 7. day
|
preoperative edema amount was subtracted from edema amount in 7. day in hyaluronidase control group
|
postoperative 7. day
|
|
evaluation of the increase of edema in postoperative 1. day using a measuring tape in dexamethasone experimental group
Time Frame: postoperative 1. day
|
preoperative edema amount was subtracted from edema amount in 1. day in dexamethasone experimental group
|
postoperative 1. day
|
|
evaluation of the increase of edema in postoperative 2. day using a measuring tape in dexamethasone experimental group
Time Frame: postoperative 2. day
|
preoperative edema amount was subtracted from edema amount in 2. day in dexamethasone experimental group
|
postoperative 2. day
|
|
evaluation of the increase of edema in postoperative 3. day using a measuring tape in dexamethasone experimental group
Time Frame: postoperative 3. day
|
preoperative edema amount was subtracted from edema amount in 3. day in dexamethasone experimental group
|
postoperative 3. day
|
|
evaluation of the increase of edema in postoperative 7. day using a measuring tape in dexamethasone experimental group
Time Frame: postoperative 7. day
|
preoperative edema amount was subtracted from edema amount in 7. day in dexamethasone experimental group
|
postoperative 7. day
|
|
evaluation of the increase of edema in postoperative 1. day using a measuring tape in dexamethasone control group
Time Frame: postoperative 1. day
|
preoperative edema amount was subtracted from edema amount in 1. day in dexamethasone controlgroup
|
postoperative 1. day
|
|
evaluation of the increase of edema in postoperative 2. day using a measuring tape in dexamethasone control group
Time Frame: postoperative 2. day
|
preoperative edema amount was subtracted from edema amount in 2. day in dexamethasone controlgroup
|
postoperative 2. day
|
|
evaluation of the increase of edema in postoperative 3. day using a measuring tape in dexamethasone control group
Time Frame: postoperative 3. day
|
preoperative edema amount was subtracted from edema amount in 3. day in dexamethasone controlgroup
|
postoperative 3. day
|
|
evaluation of the increase of edema in postoperative 7. day using a measuring tape in dexamethasone control group
Time Frame: postoperative 7. day
|
preoperative edema amount was subtracted from edema amount in 7. day in dexamethasone controlgroup
|
postoperative 7. day
|
|
evaluation of the difference in increase amounts of edema between hyaluronidase experimental and hyaluronidase control groups in postoperative 1. day using a measuring tape
Time Frame: postoperative 1. day
|
edema increase amount of hyaluronidase experimental group was compared with that of hyaluronidase control group in postoperative 1. day
|
postoperative 1. day
|
|
evaluation of the difference in increase amounts of edema between hyaluronidase experimental and hyaluronidase control groups in postoperative 2. day using a measuring tape
Time Frame: postoperative 2. day
|
edema increase amount of hyaluronidase experimental group was compared with that of hyaluronidase control group in postoperative 2. day
|
postoperative 2. day
|
|
evaluation of the difference in increase amounts of edema between hyaluronidase experimental and hyaluronidase control groups in postoperative 3. day using a measuring tape
Time Frame: postoperative 3. day
|
edema increase amount of hyaluronidase experimental group was compared with that of hyaluronidase control group in postoperative 3. day
|
postoperative 3. day
|
|
evaluation of the difference in increase amounts of edema between hyaluronidase experimental and hyaluronidase control groups in postoperative 7. day using a measuring tape
Time Frame: postoperative 7. day
|
edema increase amount of hyaluronidase experimental group was compared with that of hyaluronidase control group in postoperative 7. day
|
postoperative 7. day
|
|
evaluation of the difference in increase amounts of edema between dexamethasone experimental and dexamethasone control groups in postoperative 1. day using a measuring tape
Time Frame: postoperative 1. day
|
edema increase amount of dexamethasone experimental group was compared with that of dexamethasone control group in postoperative 1. day
|
postoperative 1. day
|
|
evaluation of the difference in increase amounts of edema between dexamethasone experimental and dexamethasone control groups in postoperative 2. day using a measuring tape
Time Frame: postoperative 2. day
|
edema increase amount of dexamethasone experimental group was compared with that of dexamethasone control group in postoperative 2. day
|
postoperative 2. day
|
|
evaluation of the difference in increase amounts of edema between dexamethasone experimental and dexamethasone control groups in postoperative 3. day using a measuring tape
Time Frame: postoperative 3. day
|
edema increase amount of dexamethasone experimental group was compared with that of dexamethasone control group in postoperative 3. day
|
postoperative 3. day
|
|
evaluation of the difference in increase amounts of edema between dexamethasone experimental and dexamethasone control groups in postoperative 7. day using a measuring tape
Time Frame: postoperative 7. day
|
edema increase amount of dexamethasone experimental group was compared with that of dexamethasone control group in postoperative 7. day
|
postoperative 7. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in hyaluronidase experimental group in postoperative 1. day
Time Frame: postoperative 1. day
|
pain intensity of the patients in hyaluronidase experimental group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 1. day
|
postoperative 1. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in hyaluronidase experimental group in postoperative 2. day
Time Frame: postoperative 2. day
|
pain intensity of the patients in hyaluronidase experimental group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 2. day
|
postoperative 2. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in hyaluronidase experimental group in postoperative 3. day
Time Frame: postoperative 3. day
|
pain intensity of the patients in hyaluronidase experimental group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 3. day
|
postoperative 3. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in hyaluronidase experimental group in postoperative 4. day
Time Frame: postoperative 4. day
|
pain intensity of the patients in hyaluronidase experimental group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 4. day
|
postoperative 4. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in hyaluronidase experimental group in postoperative 5. day
Time Frame: postoperative 5. day
|
pain intensity of the patients in hyaluronidase experimental group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 5. day
|
postoperative 5. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in hyaluronidase experimental group in postoperative 6. day
Time Frame: postoperative 6. day
|
pain intensity of the patients in hyaluronidase experimental group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 6. day
|
postoperative 6. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in hyaluronidase experimental group in postoperative 7. day
Time Frame: postoperative 7. day
|
pain intensity of the patients in hyaluronidase experimental group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 7. day
|
postoperative 7. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in hyaluronidase control group in postoperative 1. day
Time Frame: postoperative 1. day
|
pain intensity of the patients in hyaluronidase control group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 1. day
|
postoperative 1. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in hyaluronidase control group in postoperative 2. day
Time Frame: postoperative 2. day
|
pain intensity of the patients in hyaluronidase control group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 2. day
|
postoperative 2. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in hyaluronidase control group in postoperative 3. day
Time Frame: postoperative 3. day
|
pain intensity of the patients in hyaluronidase control group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 3. day
|
postoperative 3. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in hyaluronidase control group in postoperative 4. day
Time Frame: postoperative 4. day
|
pain intensity of the patients in hyaluronidase control group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 4. day
|
postoperative 4. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in hyaluronidase control group in postoperative 5. day
Time Frame: postoperative 5. day
|
pain intensity of the patients in hyaluronidase control group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 5. day
|
postoperative 5. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in hyaluronidase control group in postoperative 6. day
Time Frame: postoperative 6. day
|
pain intensity of the patients in hyaluronidase control group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 6. day
|
postoperative 6. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in hyaluronidase control group in postoperative 7. day
Time Frame: postoperative 7. day
|
pain intensity of the patients in hyaluronidase control group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 7. day
|
postoperative 7. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in dexamethasone experimental group in postoperative 1. day
Time Frame: postoperative 1. day
|
pain intensity of the patients in dexamethasone experimental group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 1. day
|
postoperative 1. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in dexamethasone experimental group in postoperative 2. day
Time Frame: postoperative 2. day
|
pain intensity of the patients in dexamethasone experimental group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 2. day
|
postoperative 2. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in dexamethasone experimental group in postoperative 3. day
Time Frame: postoperative 3. day
|
pain intensity of the patients in dexamethasone experimental group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 3. day
|
postoperative 3. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in dexamethasone experimental group in postoperative 4. day
Time Frame: postoperative 4. day
|
pain intensity of the patients in dexamethasone experimental group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 4. day
|
postoperative 4. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in dexamethasone experimental group in postoperative 5. day
Time Frame: postoperative 5. day
|
pain intensity of the patients in dexamethasone experimental group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 5. day
|
postoperative 5. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in dexamethasone experimental group in postoperative 6. day
Time Frame: postoperative 6. day
|
pain intensity of the patients in dexamethasone experimental group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 6. day
|
postoperative 6. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in dexamethasone experimental group in postoperative 7. day
Time Frame: postoperative 7. day
|
pain intensity of the patients in dexamethasone experimental group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 7. day
|
postoperative 7. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in dexamethasone control group in postoperative 1. day
Time Frame: postoperative 1. day
|
pain intensity of the patients in dexamethasone control group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 1. day
|
postoperative 1. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in dexamethasone control group in postoperative 2. day
Time Frame: postoperative 2. day
|
pain intensity of the patients in dexamethasone control group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 2. day
|
postoperative 2. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in dexamethasone control group in postoperative 3. day
Time Frame: postoperative 3. day
|
pain intensity of the patients in dexamethasone control group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 3. day
|
postoperative 3. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in dexamethasone control group in postoperative 4. day
Time Frame: postoperative 4. day
|
pain intensity of the patients in dexamethasone control group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 4. day
|
postoperative 4. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in dexamethasone control group in postoperative 5. day
Time Frame: postoperative 5. day
|
pain intensity of the patients in dexamethasone control group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 5. day
|
postoperative 5. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in dexamethasone control group in postoperative 6. day
Time Frame: postoperative 6. day
|
pain intensity of the patients in dexamethasone control group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 6. day
|
postoperative 6. day
|
|
evaluation of the pain using visual analog scale (VAS) and daily count of NSAİ drug intake in dexamethasone control group in postoperative 7. day
Time Frame: postoperative 7. day
|
pain intensity of the patients in dexamethasone control group was assessed using visual analog scale (VAS) and daily count of NSAİ drug intake in postoperative 7. day
|
postoperative 7. day
|
|
evaluation of trismus using a ruler, which measures the opening between mandibular and maxillary right first incisors of hyaluronidase experimental group preoperatively.
Time Frame: preoperative
|
amount of trismus is revealed measuring the distance between the tips of incisal edges of mandibular and maxillary right first incisors using a ruler
|
preoperative
|
|
evaluation of trismus using a ruler, which measures the opening between mandibular and maxillary right first incisors of hyaluronidase experimental group in postoperative 1. day.
Time Frame: postoperative 1. day
|
amount of trismus is revealed measuring the distance between the tips of incisal edges of mandibular and maxillary right first incisors using a ruler
|
postoperative 1. day
|
|
evaluation of trismus using a ruler, which measures the opening between mandibular and maxillary right first incisors of hyaluronidase experimental group in postoperative 2. day.
Time Frame: postoperative 2. day
|
amount of trismus is revealed measuring the distance between the tips of incisal edges of mandibular and maxillary right first incisors using a ruler
|
postoperative 2. day
|
|
evaluation of trismus using a ruler, which measures the opening between mandibular and maxillary right first incisors of hyaluronidase experimental group in postoperative 3. day.
Time Frame: postoperative 3. day
|
amount of trismus is revealed measuring the distance between the tips of incisal edges of mandibular and maxillary right first incisors using a ruler
|
postoperative 3. day
|
|
evaluation of trismus using a ruler, which measures the opening between mandibular and maxillary right first incisors of hyaluronidase experimental group in postoperative 7. day.
Time Frame: postoperative 7. day
|
amount of trismus is revealed measuring the distance between the tips of incisal edges of mandibular and maxillary right first incisors using a ruler
|
postoperative 7. day
|
|
evaluation of trismus using a ruler, which measures the opening between mandibular and maxillary right first incisors of hyaluronidase control group preoperatively.
Time Frame: preoperative
|
amount of trismus is revealed measuring the distance between the tips of incisal edges of mandibular and maxillary right first incisors using a ruler
|
preoperative
|
|
evaluation of trismus using a ruler, which measures the opening between mandibular and maxillary right first incisors of hyaluronidase control group in postoperative 1. day.
Time Frame: postoperative 1. day
|
amount of trismus is revealed measuring the distance between the tips of incisal edges of mandibular and maxillary right first incisors using a ruler
|
postoperative 1. day
|
|
evaluation of trismus using a ruler, which measures the opening between mandibular and maxillary right first incisors of hyaluronidase control group in postoperative 2. day.
Time Frame: postoperative 2. day
|
amount of trismus is revealed measuring the distance between the tips of incisal edges of mandibular and maxillary right first incisors using a ruler
|
postoperative 2. day
|
|
evaluation of trismus using a ruler, which measures the opening between mandibular and maxillary right first incisors of hyaluronidase control group in postoperative 3. day.
Time Frame: postoperative 3. day
|
amount of trismus is revealed measuring the distance between the tips of incisal edges of mandibular and maxillary right first incisors using a ruler
|
postoperative 3. day
|
|
evaluation of trismus using a ruler, which measures the opening between mandibular and maxillary right first incisors of hyaluronidase control group in postoperative 7. day.
Time Frame: postoperative 7. day
|
amount of trismus is revealed measuring the distance between the tips of incisal edges of mandibular and maxillary right first incisors using a ruler
|
postoperative 7. day
|
|
evaluation of trismus using a ruler, which measures the opening between mandibular and maxillary right first incisors of dexamethasone experimental group preoperatively.
Time Frame: preoperative
|
amount of trismus is revealed measuring the distance between the tips of incisal edges of mandibular and maxillary right first incisors using a ruler
|
preoperative
|
|
evaluation of trismus using a ruler, which measures the opening between mandibular and maxillary right first incisors of dexamethasone experimental group in postoperative 1. day.
Time Frame: postoperative 1. day
|
amount of trismus is revealed measuring the distance between the tips of incisal edges of mandibular and maxillary right first incisors using a ruler
|
postoperative 1. day
|
|
evaluation of trismus using a ruler, which measures the opening between mandibular and maxillary right first incisors of dexamethasone experimental group in postoperative 2. day.
Time Frame: postoperative 2. day
|
amount of trismus is revealed measuring the distance between the tips of incisal edges of mandibular and maxillary right first incisors using a ruler
|
postoperative 2. day
|
|
evaluation of trismus using a ruler, which measures the opening between mandibular and maxillary right first incisors of dexamethasone experimental group in postoperative 3. day.
Time Frame: postoperative 3. day
|
amount of trismus is revealed measuring the distance between the tips of incisal edges of mandibular and maxillary right first incisors using a ruler
|
postoperative 3. day
|
|
evaluation of trismus using a ruler, which measures the opening between mandibular and maxillary right first incisors of dexamethasone experimental group in postoperative 7. day.
Time Frame: postoperative 7. day
|
amount of trismus is revealed measuring the distance between the tips of incisal edges of mandibular and maxillary right first incisors using a ruler
|
postoperative 7. day
|
|
evaluation of trismus using a ruler, which measures the opening between mandibular and maxillary right first incisors of dexamethasone control group preoperatively.
Time Frame: preoperative
|
amount of trismus is revealed measuring the distance between the tips of incisal edges of mandibular and maxillary right first incisors using a ruler
|
preoperative
|
|
evaluation of trismus using a ruler, which measures the opening between mandibular and maxillary right first incisors of dexamethasone control group in postoperative 1. day.
Time Frame: postoperative 1. day
|
amount of trismus is revealed measuring the distance between the tips of incisal edges of mandibular and maxillary right first incisors using a ruler
|
postoperative 1. day
|
|
evaluation of trismus using a ruler, which measures the opening between mandibular and maxillary right first incisors of dexamethasone control group in postoperative 2. day.
Time Frame: postoperative 2. day
|
amount of trismus is revealed measuring the distance between the tips of incisal edges of mandibular and maxillary right first incisors using a ruler
|
postoperative 2. day
|
|
evaluation of trismus using a ruler, which measures the opening between mandibular and maxillary right first incisors of dexamethasone control group in postoperative 3. day.
Time Frame: postoperative 3. day
|
amount of trismus is revealed measuring the distance between the tips of incisal edges of mandibular and maxillary right first incisors using a ruler
|
postoperative 3. day
|
|
evaluation of trismus using a ruler, which measures the opening between mandibular and maxillary right first incisors of dexamethasone control group in postoperative 7. day.
Time Frame: postoperative 7. day
|
amount of trismus is revealed measuring the distance between the tips of incisal edges of mandibular and maxillary right first incisors using a ruler
|
postoperative 7. day
|
|
evaluation of infection in operation site via determination of infection signs in physical examination of hyaluronidase experimental group preoperatively.
Time Frame: preoperative
|
existence of infection signs were determined using physical examination method.
if the count of + signs are more than half of total amount of determined signs, the evaluation is accepted as (+) infected.
|
preoperative
|
|
evaluation of infection in operation site via determination of infection signs in physical examination of hyaluronidase experimental group in postoperative 1. day.
Time Frame: postoperative 1. day
|
existence of infection signs were determined using physical examination method.
if the count of + signs are more than half of total amount of determined signs, the evaluation is accepted as (+) infected.
|
postoperative 1. day
|
|
evaluation of infection in operation site via determination of infection signs in physical examination of hyaluronidase experimental group in postoperative 2. day.
Time Frame: postoperative 2. day
|
existence of infection signs were determined using physical examination method.
if the count of + signs are more than half of total amount of determined signs, the evaluation is accepted as (+) infected.
|
postoperative 2. day
|
|
evaluation of infection in operation site via determination of infection signs in physical examination of hyaluronidase experimental group in postoperative 3. day.
Time Frame: postoperative 3. day
|
existence of infection signs were determined using physical examination method.
if the count of + signs are more than half of total amount of determined signs, the evaluation is accepted as (+) infected.
|
postoperative 3. day
|
|
evaluation of infection in operation site via determination of infection signs in physical examination of hyaluronidase experimental group in postoperative 7. day.
Time Frame: postoperative 7. day
|
existence of infection signs were determined using physical examination method.
if the count of + signs are more than half of total amount of determined signs, the evaluation is accepted as (+) infected.
|
postoperative 7. day
|
|
evaluation of infection in operation site via determination of infection signs in physical examination of hyaluronidase control group preoperatively.
Time Frame: preoperative
|
existence of infection signs were determined using physical examination method.
if the count of + signs are more than half of total amount of determined signs, the evaluation is accepted as (+) infected.
|
preoperative
|
|
evaluation of infection in operation site via determination of infection signs in physical examination of hyaluronidase control group in postoperative 1. day.
Time Frame: postoperative 1. day
|
existence of infection signs were determined using physical examination method.
if the count of + signs are more than half of total amount of determined signs, the evaluation is accepted as (+) infected.
|
postoperative 1. day
|
|
evaluation of infection in operation site via determination of infection signs in physical examination of hyaluronidase control group in postoperative 2. day.
Time Frame: postoperative 2. day
|
existence of infection signs were determined using physical examination method.
if the count of + signs are more than half of total amount of determined signs, the evaluation is accepted as (+) infected.
|
postoperative 2. day
|
|
evaluation of infection in operation site via determination of infection signs in physical examination of hyaluronidase control group in postoperative 3. day.
Time Frame: postoperative 3. day
|
existence of infection signs were determined using physical examination method.
if the count of + signs are more than half of total amount of determined signs, the evaluation is accepted as (+) infected.
|
postoperative 3. day
|
|
evaluation of infection in operation site via determination of infection signs in physical examination of hyaluronidase control group in postoperative 7. day.
Time Frame: postoperative 7. day
|
existence of infection signs were determined using physical examination method.
if the count of + signs are more than half of total amount of determined signs, the evaluation is accepted as (+) infected.
|
postoperative 7. day
|
|
evaluation of infection in operation site via determination of infection signs in physical examination of dexamethasone experimental group preoperatively.
Time Frame: preoperative
|
existence of infection signs were determined using physical examination method.
if the count of + signs are more than half of total amount of determined signs, the evaluation is accepted as (+) infected.
|
preoperative
|
|
evaluation of infection in operation site via determination of infection signs in physical examination of dexamethasone experimental group in postoperative 1. day
Time Frame: postoperative 1. day
|
existence of infection signs were determined using physical examination method.
if the count of + signs are more than half of total amount of determined signs, the evaluation is accepted as (+) infected.
|
postoperative 1. day
|
|
evaluation of infection in operation site via determination of infection signs in physical examination of dexamethasone experimental group in postoperative 2. day
Time Frame: postoperative 2. day
|
existence of infection signs were determined using physical examination method.
if the count of + signs are more than half of total amount of determined signs, the evaluation is accepted as (+) infected.
|
postoperative 2. day
|
|
evaluation of infection in operation site via determination of infection signs in physical examination of dexamethasone experimental group in postoperative 3. day
Time Frame: postoperative 3. day
|
existence of infection signs were determined using physical examination method.
if the count of + signs are more than half of total amount of determined signs, the evaluation is accepted as (+) infected.
|
postoperative 3. day
|
|
evaluation of infection in operation site via determination of infection signs in physical examination of dexamethasone experimental group in postoperative 7. day
Time Frame: postoperative 7. day
|
existence of infection signs were determined using physical examination method.
if the count of + signs are more than half of total amount of determined signs, the evaluation is accepted as (+) infected.
|
postoperative 7. day
|
|
evaluation of infection in operation site via determination of infection signs in physical examination of dexamethasone control group preoperatively.
Time Frame: preoperatively
|
existence of infection signs were determined using physical examination method.
if the count of + signs are more than half of total amount of determined signs, the evaluation is accepted as (+) infected.
|
preoperatively
|
|
evaluation of infection in operation site via determination of infection signs in physical examination of dexamethasone control group in postoperative 1. day
Time Frame: postoperative 1. day
|
existence of infection signs were determined using physical examination method.
if the count of + signs are more than half of total amount of determined signs, the evaluation is accepted as (+) infected.
|
postoperative 1. day
|
|
evaluation of infection in operation site via determination of infection signs in physical examination of dexamethasone control group in postoperative 2. day
Time Frame: postoperative 2. day
|
existence of infection signs were determined using physical examination method.
if the count of + signs are more than half of total amount of determined signs, the evaluation is accepted as (+) infected.
|
postoperative 2. day
|
|
evaluation of infection in operation site via determination of infection signs in physical examination of dexamethasone control group in postoperative 3. day
Time Frame: postoperative 3. day
|
existence of infection signs were determined using physical examination method.
if the count of + signs are more than half of total amount of determined signs, the evaluation is accepted as (+) infected.
|
postoperative 3. day
|
|
evaluation of infection in operation site via determination of infection signs in physical examination of dexamethasone control group in postoperative 7. day
Time Frame: postoperative 7. day
|
existence of infection signs were determined using physical examination method.
if the count of + signs are more than half of total amount of determined signs, the evaluation is accepted as (+) infected.
|
postoperative 7. day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 1, 2019
Primary Completion (Actual)
June 30, 2022
Study Completion (Actual)
June 30, 2022
Study Registration Dates
First Submitted
July 13, 2022
First Submitted That Met QC Criteria
July 15, 2022
First Posted (Actual)
July 20, 2022
Study Record Updates
Last Update Posted (Actual)
July 20, 2022
Last Update Submitted That Met QC Criteria
July 15, 2022
Last Verified
July 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Pathologic Processes
- Nervous System Diseases
- Infections
- Postoperative Complications
- Neurologic Manifestations
- Neuromuscular Manifestations
- Wound Infection
- Spasm
- Edema
- Surgical Wound Infection
- Trismus
- Physiological Effects of Drugs
- Autonomic Agents
- Peripheral Nervous System Agents
- Anti-Inflammatory Agents
- Antineoplastic Agents
- Antiemetics
- Gastrointestinal Agents
- Glucocorticoids
- Hormones
- Hormones, Hormone Substitutes, and Hormone Antagonists
- Antineoplastic Agents, Hormonal
- Dexamethasone
Other Study ID Numbers
- YDU/2019//74-921
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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