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Comparison of analgesic effect of rupivacaine with dexamethasone and rupivacaine with dexmedetomidine

Phase 3
Recruiting
Conditions
Post procedural pain.
Other acute postprocedural pain
G89.18
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
NameTimeMethod
Pain of patients after cesarean section. Timepoint: 24 hours after surgery. Method of measurement: By visual analog scale questionnaire.
Secondary Outcome Measures
NameTimeMethod
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