The effect of pre-operative oral pregabalin on pain after laparoscopic surgeries for endometriosis in wome
Phase 3
- Conditions
- aparoscopic surgeries for endometriosis in women.Endometriosis
- Registration Number
- IRCT20230812059132N1
- Lead Sponsor
- Iran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
Patients aged between 18-45 years
All patients who are candidates for laparoscopic endometriosis surgery
Absence of drug addiction in the patient
Lack of chronic and long-term use of opioid drugs or painkillers such as tramadol, diclofenac, naproxen
Do not have psychiatric problems
Insensitivity to pregabalin
Performing surgery between 1401 and 1402 in Rasul Akram Hospital
Exclusion Criteria
have a contraindication for laparoscopy
Have liver or kidney problems
BMI above 30
Not able to express VAS score
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: All patients in two groups are evaluated after surgical recovery and immediately after recovery and at 2, 6, 12, 24 and 48 hours after surgery. Method of measurement: In terms of the amount of pain, they will be assessed by the visual pain assessment questionnaire (VAS).
- Secondary Outcome Measures
Name Time Method