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Patient-controlled analgesia versus intrathecal opioid for pain after cesarean sectio

Phase 3
Conditions
Post-cesarean section pain.
Other acute postprocedural pain
G89.18
Registration Number
IRCT20220411054492N1
Lead Sponsor
Vice-Chancellery for Research Hormozgan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
60
Inclusion Criteria

Pregnancy
Elective cesarean section
ASA class I and II
Age: 18-46 years old

Exclusion Criteria

Emergency cesarean section
Complications during cesarean section

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Patient satisfaction with analgesia. Timepoint: After gaining consciousness in the recovery and then at 1, 4, and 24 hours in the ward. Method of measurement: Numerical rating scale (NRS).
Secondary Outcome Measures
NameTimeMethod
Drug side effects. Timepoint: Up to 24 hours after surgery. Method of measurement: Pruritus, nausea and/or vomiting, and respiratory depression (respiratory rate <10/min).
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