Comparison of the effect of Fentanyl and Sufentanil added to Bupivacaine on post-cesarean pain.

Phase 2

Completed

• Conditions: Pain after cesarean section.; Delivery; 080-084

• Registration Number: IRCT2016101530303N1
• Lead Sponsor: Vice Chancellor for research of Hormozgan University of Medical Sciences, Bandar Abbas.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 22 February 2018

Recruitment & Eligibility

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

Inclusion Criteria

class ? or ? of ASA (American Society of Anesthesiologists; candidate for elective cesarean section; no history of heart disease, hypertension, preeclampsia, gestational diabetes; being satisfied to receive intrathecal anesthesia and participate in the study. Exclusion criteria: contraindication for spinal anesthesia; presence of infection in the needle insertion site; high intracranial pressure; coagulopathy; platelet count lower than 75000.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The numbness. Timepoint: 3 times (every 8 hours) in the first 24 hours. Method of measurement: Questionnaire.;Blood Pressure. Timepoint: Monitoring during the first 24 hours. Method of measurement: Questionnaire.;Analgesia. Timepoint: 3 times (every 8 hours) in the first 24 hours. Method of measurement: Questionnaire.

Secondary Outcome Measures

Name	Time	Method
ausea and vomiting. Timepoint: 3 times (every 8 hours) in the first 24 hours. Method of measurement: Questionnaire.