Evaluation of the effect of fentanyl or sulfentanil on spinal anesthesia in cesarean sectio

Phase 2

Recruiting

• Conditions: Cesarean section.; Onset (spontaneous) of labor after 37 completed weeks of gestation but before 39 completed weeks gestation, with delivery by (planned) cesarean section; O75.82

• Registration Number: IRCT20171109037340N1
• Lead Sponsor: Zahedan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 26 March 2018

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 90

Inclusion Criteria

Term pregnancy
Primigravida
ASA class 1 and 2
Cesarean section due to cephalopelvic disproportion

Exclusion Criteria

spinal anesthesia contraindication
Gestational hypertension
Gestational diabetes
Placenta previa

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Analgesia quality. Timepoint: Immediately after drug injection. Method of measurement: Based on 4 grades; Excellent: During the procedure, patients feel comfortable with no complainment. Good: brief discomfort with no need of additional medication. Moderate: Unpleasant but controllable with additional medication such as phenthanyl, propofol, dormicom and the like. Poor: Inability to control even with an additional drug.;The duration of effective analgesia. Timepoint: The interval between the initiation of drug administration in each group until the first request of analgesia by patients. Method of measurement: 1-awake and anxious; 2- awake and calm; 3- sleepy but easily awake; 4- sleepy but not easily awake.;Duration of discharge. Timepoint: The interval between the initiation of drug administration in each group until the time of discharge from hospital. Method of measurement: Day.