Transdermaal patches for pain relief following Oral surgery
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/09/036381
- Lead Sponsor
- ITHISH SANKEPALLY
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Both Male and Female Patients undergoing orthognathic surgery and willing or giving consent for surgery
Exclusion Criteria
Age group below 18 years and above 35 years
Patients not willing for surgery
Patients with known skin allergies.
Patients with allergies to diclofenac
Patients with systemic complications.
Patients with known hepatic and renal issues
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method pain assessment following surgery using visual analogue scaleTimepoint: 2hrs, 6hrs,12hrs, 18hrs ,24 hrs following surgery
- Secondary Outcome Measures
Name Time Method The need to delay or decrease the need of rescue analgesicTimepoint: Based on Visual Analogue Scale, if patient score exceeds 5, a rescue analgesic is administered to ease post-operative pain.