The effect of adding sufentanil to rupivacaine 0.5% and sufentanil to bupivacaine 0.5% on analgesia and chills during and after surgery in subjects undergoing elective cesarean sectio

Phase 1

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: IRCT20130926014779N7
• Lead Sponsor: Jahrom University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 September 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 60

Inclusion Criteria

Interest in participating in the study
No chronic pain and cancer
No hearing or verbal impairment
Hemodynamic stability
No infection at the site of needle entry
Not High intracranial pressure
No coagulation disorders

Exclusion Criteria

People who need medication or action other than routine care during surgery to relieve complications and reduce pain.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Before the spinal, after the spinal and during the change of position of the patient and then every 15 minutes to the first hour and also during the entry into recovery and when leaving the recovery and finally three and six hours after the operation. Method of measurement: Pain assessment ruler.;Shivering. Timepoint: Before the spinal, after the spinal and during the change of position of the patient and then every 15 minutes to the first hour and also during the entry into recovery and when leaving the recovery and finally three and six hours after the operation. Method of measurement: Shivering scale.