PAIN CONTROL FOLLOWING THE ADMINISTRATION OF DICLOFENAC SODIUM BY TRANSBUCCAL PATCH VERSUS THE CONVENTIONAL PERORAL ROUTE AFTER ROUTINE DENTAL EXTRACTIONS.
Phase 1
Not yet recruiting
- Registration Number
- CTRI/2023/06/054214
- Lead Sponsor
- terna dental college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
a) Patients aged between 18 to 65 years
b) Without any systemic disease or drug allergy
c) Patients indicated for posterior tooth extraction classified with similar difficulty index.
d) Interval between two extractions appointments should be at least a minimum of 7 days.
Exclusion Criteria
a) Smokers (current or former)
b) Alcoholics or narcotic abusers.
c) Condition of pregnancy or lactation.
d) Medically compromised patients.
e) Tooth with different difficulty index.
f) Tooth with any grade of mobility or periodontally compromised tooth.
g) Patients with the pathology associated with respect to their tooth indicated for extraction
h) Patients not to be on any opioid analgesics and/or NSAIDs except diclofenac sodium.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method PAIN RELIEFTimepoint: Pain is to be checked on the VAS scale after every 24 hours for 3 days post-extraction.
- Secondary Outcome Measures
Name Time Method To check the efficacy of the patch in comparison to the conventional peroral route .Timepoint: 1 year