Transverses Abdominis Plane Block Versus Local Wound Infiltration in Total Abdominal Hysterectomy

NCT ID: NCT06256302

Last Updated: 2024-07-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-12-01

Study Completion Date

2024-02-28

Brief Summary

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To compare the transverses abdominis plane block outcome versus local wound infiltration for postoperative analgesia in patients undergoing total abdominal hysterectomy.

Detailed Description

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Conditions

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Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

DOUBLE

Participants Caregivers

Study Groups

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Transverses abdominis plane block

Group Type EXPERIMENTAL

Transverses Abdominis Plane Block

Intervention Type PROCEDURE

Transverses abdominis plane block will be provided randomly using prospective double-blinding.

Local wound infiltration

Group Type ACTIVE_COMPARATOR

Local wound infiltration

Intervention Type PROCEDURE

Local wound infiltration will be provided randomly using prospective double-blinding.

Interventions

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Transverses Abdominis Plane Block

Transverses abdominis plane block will be provided randomly using prospective double-blinding.

Intervention Type PROCEDURE

Local wound infiltration

Local wound infiltration will be provided randomly using prospective double-blinding.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Age range 18 to 50 years
* Female
* ASA I \& II
* Undergoing Abdominal Hysterectomy under General anaesthesia

Exclusion Criteria

* Hepatic failure (assessed on clinical signs and symptoms, elevated liver enzymes and ultrasound findings showing loss of normal texture of liver) or renal failure (a GFR of 15 or less)
* Allergy or contraindication to study drugs on history
* Drug abuse or addiction
* Bleeding tendency
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Dr Muhammad Arif

OTHER

Sponsor Role lead

Responsible Party

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Dr Muhammad Arif

Principal Investigator

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Muhammad Arif

Role: PRINCIPAL_INVESTIGATOR

Ziauddin University

Locations

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Muhammad Arif

Karachi, Sindh, Pakistan

Site Status

Countries

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Pakistan

Other Identifiers

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7861023MAANE

Identifier Type: -

Identifier Source: org_study_id

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