- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06427070
Effectiveness of Two Intracanal Irrigation Solutions
May 18, 2024 updated by: Manal Mohamed, Misr University for Science and Technology
Effectiveness of Two Intracanal Irrigation Solutions Delivered Through Cryotherapy on Post-Endodontic Pain Relieve. A Randomized Clinical Trial
The aim of the present clinical trial is to investigate and compare the effect of crayotherapy utilizing two intra-canal final irrigating solutions on postoperative pain.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
- st: Comparison of pain reduction algorism after cryotherapy using the two tested irrigating materials
- nd. Number and frequency of analgesics taken for pain relief during one week postoperative
Study Type
Interventional
Enrollment (Estimated)
1
Phase
- Not Applicable
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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Case diagnosed as having symptomatic irreversible pulpitis with symptomatic apical periodontitis
- Patients requiring emergency RCT
- Pre-operative pain score 7 on Numerical Rating (NRS) scale
- Middle aged males (25-50)
- Medical profile ASA1
- Willing to sign the consent form
- Willing to answer our call for one week period
Exclusion Criteria:
- Females
- Medical conditions above ASA1
- Multi-rooted teeth
- Patients younger or older than (25-50)
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: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Irrigating solutions
Group 1 sodium hypochlorite Group 2 saline Group 3 chlorohexidine
|
Saline, sodium hypochlorite, chlorohexidine
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
pain scale
Time Frame: 1 week
|
pain scale Comparison of the 2 selected irrigating solutions
|
1 week
|
|
Analgesics Frequency
Time Frame: 1 week
|
Frequency of analgesics for pain relief
|
1 week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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 (Estimated)
May 23, 2024
Primary Completion (Estimated)
May 30, 2024
Study Completion (Estimated)
June 1, 2024
Study Registration Dates
First Submitted
May 14, 2024
First Submitted That Met QC Criteria
May 18, 2024
First Posted (Actual)
May 23, 2024
Study Record Updates
Last Update Posted (Actual)
May 23, 2024
Last Update Submitted That Met QC Criteria
May 18, 2024
Last Verified
May 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CHX 2024
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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