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NCT06256302 Clinical Trial

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

Pain Clinical Trial

Official title:
Transverses Abdominis Plane Block Versus Local Wound Infiltration for Postoperative Pain Management in Patients Undergoing Total Abdominal Hysterectomy

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT06256302
Other study ID # 7861023MAANE
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date December 1, 2023
Est. completion date February 28, 2024

Study information
Verified date February 2024
Source Ziauddin University
Contact Muhammad Arif
Phone +923313455112
Email muhammad.aarif@zu.edu.pk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date February 28, 2024
Est. primary completion date February 28, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 50 Years
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Transverses Abdominis Plane Block
Transverses abdominis plane block will be provided randomly using prospective double-blinding.
• Local wound infiltration
Local wound infiltration will be provided randomly using prospective double-blinding.

Locations
Country Name City State
Pakistan Muhammad Arif Karachi Sindh

Sponsors (1)
Lead Sponsor Collaborator
Dr Muhammad Arif

Country where clinical trial is conducted

Pakistan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain score Pain score will be evaluated through Visual analogue scale (VAS) score of 0-10cms. 24 hours of surgery.
Secondary Analgesia consumption Patients will be given analgesics only on complain of pain of VAS score of 4 and above. During 24 hours of surgery
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