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Duration of analgesia after cesarean section with Ropivacaine-Fentanyl and Ropivacaine-Sufentanil

Phase 3
Recruiting
Conditions
Pain after cesarean section.
Pain, not elsewhere classified
Registration Number
IRCT20210827052297N1
Lead Sponsor
Ahvaz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
44
Inclusion Criteria

Age between 17 to 45 years old
ASA Class I and II
Candidate for elective cesarean section
No allergies to fentanyl, sufentanil and ropivacaine
no history of addiction
Consent to participate in the study

Exclusion Criteria

Severe liver disease
Need for general anesthesia

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Duration of analgesia. Timepoint: After entering the recovery room, then every 15 minutes until the first hour, then every hour for 12 hours. Method of measurement: The duration of analgesia is the time of performing spinal anesthesia to Visual analog scale (VAS) grade 3.;Systolic blood pressure. Timepoint: At the beginning of the study (before the intervention) and then every 5 minutes until end of recovery. Method of measurement: Mercury barometer.;Diastolic blood pressure. Timepoint: At the beginning of the study (before the intervention) and then every 5 minutes until end of recovery. Method of measurement: Mercury barometer.
Secondary Outcome Measures
NameTimeMethod
ausea after surgery. Timepoint: In the first 12 hours after surgery. Method of measurement: Presence of nausea based on direct observation and patients report.;Vomiting after surgery. Timepoint: In the first 12 hours after surgery. Method of measurement: Presence of vomiting based on direct observation and patients report.
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