Actively Recruiting

Phase 1
Phase 2
Age: 25Years - 65Years
FEMALE
NCT07482709

Comparison Between Tranversus Abdominis Plane (TAP) Block With Only Bupivacaine and TAP Block With Bupivacaine Plus Ketamine in Reducing Postoperative Pain After Total Abdominal Hystrectomy

Led by Liaquat National Hospital & Medical College · Updated on 2026-03-25

30

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this study is to know how effectively TAP block can reduce postoperative pain in total abdominal hystrectomy patients when given ketamine in addition to bupivacaine in TAP block and to compare it with the conventional TAP block with bupivacaine only. The main question it aims to answer is: Does intervention with ketamine in TAP block lowers the postoperative pain measured via visual analog scale and decreases the need for rescue analgesia? Patients will be assessed for pain in PACU( post anesthesia care unit), 6 hours, 12 hours and 24 hours postoperatively. Time of rescue analgesia will also be noted if given.

CONDITIONS

Official Title

Comparison Between Tranversus Abdominis Plane (TAP) Block With Only Bupivacaine and TAP Block With Bupivacaine Plus Ketamine in Reducing Postoperative Pain After Total Abdominal Hystrectomy

Who Can Participate

Age: 25Years - 65Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged between 25 to 60 years
  • ASA grade I & II
  • Undergoing total abdominal hysterectomy
Not Eligible

You will not qualify if you...

  • Body mass index over 35 kg/m2
  • Patient refusal to participate
  • Coagulation disorders
  • History of allergy or hypersensitivity to local anesthetics
  • Infection at the injection site
  • Alcohol or drug abuse
  • Cognitive or mental disorders

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

gynae operation theatre at Liaquat National Hospital

Karachi, Sindh, Pakistan, 74800

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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