Bupivacain and Fentanyl, before the start of surgery or before the end of surgery?
Phase 2
- Conditions
- local analgesia in major gynecologic surgeries.Unspecified condition associated with female genital organs and menstrual cycle
- Registration Number
- IRCT201107127013N1
- Lead Sponsor
- Tabriz Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 50
Inclusion Criteria
(being over 18 years; having indication for major gynecologic surgery)
Exclution criteria: (to have a contraindication for epidural analgesia; to have allergy to local anesthetics; to have mental disorders; organic dysfunctions; previous chronic pain)
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain severity. Timepoint: 0, 3, 6, 12 and 24 hours after becoming conscious. Method of measurement: using visual pain scoring (VAS) from 0 (without pain) to 10 (severe intolerable pain).;Analgesics administered dose. Timepoint: 0-3-6-12-24 hours after becoming conscious. Method of measurement: Injection count and injection dose in milli or micro grams.
- Secondary Outcome Measures
Name Time Method