- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01945502
Nasopharyngeal Packing and Rhinologic Surgery.
September 16, 2013 updated by: Basak Ceyda MECO
The Effectiveness of Three Different Nasopharyngeal Packing on the Prevention of Postoperative Nausea- Vomiting and Postoperative Throat Pain in Rhinologic Surgery.
The purpose of this study is to assess the efficacy of three different pharyngeal packing during routine rhinologic surgery in the prevention of postoperative nausea and vomiting, and to evaluate the influence of pharyngeal packing on postoperative throat pain.
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
120
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Ankara, Turkey, 06100
- Recruiting
- Ankara University Faculty of Medicine ENT operating rooms
-
Contact:
- Basak Ceyda MECO, MD, DESA
- Phone Number: 0090 532 4179911
- Email: basakceyda@hotmail.com
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-
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
18 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Adult patients (18-60 years) scheduled for routine nasal and/or paranasal sinus surgeries in Ankara Univerity Faculty of Medicine, ETN operating rooms were recruited into this study.
Description
Inclusion Criteria:
- 18-60 years old adult patient
- nasal and/or paranasal sinus surgeries
- general anesthesia
Exclusion Criteria:
- patients submitted to another intervention at the same time (adenoidectomy, tonsillectomy)
- patients with a serious systemic disease (acquired immunodeficiency syndrome,leukemia, lymphoma, or other neoplasias under chemotherapy treatment)
- patients presenting contraindications for using nonsteroid anti-inflammatory drugs
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
Cohorts and Interventions
Group / Cohort |
---|
nasal packing with dry packs
|
nasal packing with wet packs
|
nasal packing with Benzidamin-Clorhexsidin damped packs
|
no nasal packing
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Postoperative nausea vomiting
Time Frame: 3 months
|
3 months
|
sore throat
Time Frame: 3 months
|
3 months
|
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
September 1, 2013
Primary Completion (Anticipated)
December 1, 2013
Study Registration Dates
First Submitted
September 16, 2013
First Submitted That Met QC Criteria
September 16, 2013
First Posted (Estimate)
September 18, 2013
Study Record Updates
Last Update Posted (Estimate)
September 18, 2013
Last Update Submitted That Met QC Criteria
September 16, 2013
Last Verified
September 1, 2013
More Information
Terms related to this study
Other Study ID Numbers
- 11-434-13
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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