Comparison of the administration time of diclofenac suppository on post-operative pain in transvaginal oocyte retrieval under general anesthesia in infertile wome
Phase 2
- Conditions
- Female infertility.Female infertility
- Registration Number
- IRCT20120215009014N259
- Lead Sponsor
- Hamedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 70
Inclusion Criteria
Age of 18 to 45 years;
Infertile women candidate for IVF
Exclusion Criteria
A previous history of IVF;
Number of follicles less than two;
Using NSAIDS or alcohol;
Sensitivity to diclofenac;
Psychological problems;
A history of convulsion;
Chronic disease such as hepatitis, renal failure, cardiovascular, peptic ulcer, inflammatory bowel disease
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assessing the pain. Timepoint: At 15, 30, 60, and 120 minutes after operation. Method of measurement: Using visual analog scale (VAS).
- Secondary Outcome Measures
Name Time Method Assessing the nausea and vomiting. Timepoint: At 15, 30, 60, and 120 minutes after operation. Method of measurement: By physical examination and history taking.