Effect of topical application of piroxicam gel, diclofenac gel and emla on pain relief
Not Applicable
Recruiting
- Conditions
- intensity of pain.Pain, not elsewhere classified
- Registration Number
- IRCT20180107038251N8
- Lead Sponsor
- Arak University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 123
Inclusion Criteria
Age range from 15 to 65 years of old
ASA I , II
Absence of pain for any reason
Absence of verbal, mental and visual disability
Absence of pregnancy
No history of drug abuse
Not using painkillers in the last 24 hours
Absence of sensitivity to NSAID
Absence of sensitivity to local anesthetics
Absence of allergy to vitamin A + D ointment
Exclusion Criteria
Lack of patient consent to participate or continue the study
Body mass index more than 30
Presence of peripheral vascular disease and Raynaud's syndrome
The presence of scleroderma
Failure of the researcher in the first attempt at cannulation
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intensity of pain. Timepoint: at 0, 5, 10, 15, 30, and 45 minutes after cannulation. Method of measurement: Visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method