TAP Block In Area with Limited Resources

Not Applicable

• Conditions: Surgery; Pain Management

• Registration Number: PACTR201704002165131
• Lead Sponsor: ational Board For Higher Education

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-04-01
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 108

Inclusion Criteria

¿Mothers with body mass index ¿ 30 kg/m2)
¿All mothers classified as ASA I/II
¿Patients under spinal anesthesia
¿All emergency and elective patients who are scheduled for Pfannenstiel incision under spinal anesthesia

Exclusion Criteria

¿Patients with any history of allergy to the drugs used in this study
¿Obesity (body mass index ¿ 30 kg/m2)
¿Local infection at the injection site of the TAP
¿Patients with cardiovascular, pulmonary and neurological diseases
¿Patients requiring general anesthesia for obstetric or anesthetic reasons
¿Patients undergoing upper segment caesarean section
¿Maternal or fetal compromise

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary outcome of the study was visual analog scale pain score in the first 24 postoperative hours

Secondary Outcome Measures

Name	Time	Method
Reduction in the consumption of morphine and diclofenac postoperatively;Reduction in the postoperative side effects of morphine