comparing two methods of providing pain relief after surgery

Not Applicable

• Conditions: Health Condition 1: null- patients posted for total abdominal hysterectomy in JIPMER

• Registration Number: CTRI/2017/06/008798
• Lead Sponsor: Jawaharlal Institute of Postgraduate Medical Education and Research

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Open to Recruitment
• Sex: Not specified
• Target Recruitment: 100

Inclusion Criteria

1. ASA1 or ASA2 status

2. patients undergoing total abdominal hysterectomy

Exclusion Criteria

patients with contra indication to regional anesthesia, allergy to local anesthetics, unwilling for study

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
post operative pain assessment using VAS scoresTimepoint: 24 months

Secondary Outcome Measures

Name	Time	Method
comparison of hemodynamics, opioid consumption, opioid side effects, length of hospital stay, patient satisfaction scoreTimepoint: 24 months