Evaluation of the effect of gabapentin in reducing pai
Phase 3
Recruiting
- Conditions
- Reduction of pain after laparoscopic endometriosis surgery.
- Registration Number
- IRCT20150817023666N14
- Lead Sponsor
- Iran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 140
Inclusion Criteria
Endometriosis patients aged 16-40 years in Stage 3 and 4 diseases
Exclusion Criteria
Kidney and liver patients
patients with gabapentin allergy
patients with mental disorders and epilepsy
patients who have taken painkillers and any drugs and cigarettes one week before surgery
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduction of pain and drug use after laparoscopic surgery. Timepoint: 6, 12 and 24 hours after surgery. Method of measurement: Pain questionnaire based on Visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method