Comparison between the effect of two antibacterial gels on reducing the incidence of dry socket after wisdom teeth surgery
Not Applicable
- Conditions
- Dry Socket.
- Registration Number
- IRCT2017082735916N1
- Lead Sponsor
- Qazvin University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Male
- Target Recruitment
- 90
Inclusion Criteria
man 15-60 years old; completely healthy in terms of systemic conditions (ASA I); at least one mandibular third molar with moderate difficulty; able to filling VAS questionnaire.
exclusion criteria: History of smoking; Taking systemic antibiotics or taking antibiotics over the last 24 hours; The length of the surgical time is more than thirty minutes; Having any history of allergies; History of gastric ulcer or any digestive problem; Not attending follow-up meetings. Use of any other drugs as post-surgical medication; Mental inability to give informed consent.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reducing the prevalevce of dry socket. Timepoint: third day after surgery (follow up). Method of measurement: postoperative pain in and around the extraction site, which increases in severity at any time between 1 and 3 days after the extraction accompanied by a partially or totally disintegrated blood clot within the alveolar socket with or without halitosis. It has been identified with the scale of Has / has not happened.;Decreasing the Severity of pain. Timepoint: from 1st to 7th days after surgery. Method of measurement: according to the VAS questionare.
- Secondary Outcome Measures
Name Time Method Any side effects after using each gels. Timepoint: during the first week after surgery. Method of measurement: patients had researcher's phone number to call if they had any problems or questions.