Comparison of analgesic effect of rupivacaine with dexamethasone and rupivacaine with dexmedetomidine
Phase 3
Recruiting
- Conditions
- Post procedural pain.Other acute postprocedural painG89.18
- Registration Number
- IRCT20210302050553N1
- Lead Sponsor
- Zanjan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
ASA(American Society of Anesthesiologists) grade 1 or 2
The patient's ability to report the extent of their pain by criteria VAS(visual analog scale)
Conscious consent of the patient to participate in the study
Candidate for cesarean section under anesthesia with TAP(transverse abdominis plane) block
Exclusion Criteria
History of anaphylaxis to dexmedetomidine or ropivacaine
History of drug abuse
History of coagulopathy
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain of patients after cesarean section. Timepoint: 24 hours after surgery. Method of measurement: By visual analog scale questionnaire.
- Secondary Outcome Measures
Name Time Method