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The Effects of Transversus Abdominis Plane Block in Patients Undergoing Total Abdominal Hysterectomy (TAP)

T

Tokat Gaziosmanpasa University

Status and phase

Completed
Phase 4

Conditions

Intraoperative Complications
Abdominal Hysterectomy (& Wertheim)

Treatments

Procedure: Control
Procedure: TAP block

Study type

Interventional

Funder types

Other

Identifiers

NCT02296619
GaziosmanpashaU

Details and patient eligibility

About

The purpose of this study is to determine the effects of Transversus Abdominis Plane Block on hemodynamic variables, anaesthetic and analgesic requirement, and quality of recovery in patients undergoing total abdominal hysterectomy

Full description

Pain is one of the main causes of the poor perioperative outcomes and pain management is the important part of perioperative period. Neuraxial blocks could provide adequate analgesia during and after abdominal surgery. However,neuraxial blocks have a lot of contraindicated situations and neuraxial anesthesia can easily induce hemodynamic abnormalities. Therefore, in most cases, the choice of anaesthetic management may be the general anesthesia. In addition to reduce the blood pressure and heart rate changes due to surgical stimulations, the large amount of opioids and anaesthetics may be required. Opioid related side effects can affect perioperative complications and postoperative quality of recovery. Transversus abdominis plane block is a new choice to reduce postoperative pain in abdominal surgery. Although its postoperative analgesic efficacy is well known, its effects on hemodynamic variables, anaesthetic and analgesic requirement is not clear. The main objective of this study is to estimate the effect of Transversus abdominis plane block on hemodynamic variables, anaesthetic and analgesic requirement and quality of recovery in patients undergoing total abdominal hysterectomy.

Enrollment

66 patients

Sex

Female

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult (18-65years old)
  • American Society of Anesthesiologists (ASA) physical status I-II
  • Patients scheduled for elective total abdominal hysterectomy under general anesthesia

Exclusion criteria

  • ASA physical status ≥ 3
  • Allergy to local anesthetics
  • Drug abuse or addiction
  • Bleeding tendency

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

66 participants in 2 patient groups

TAP Block
Experimental group
Description:
Using real time ultrasound imaging, bilateral, 20 ml 0,25% bupivacaine inject into the area between the internal oblique and transverse abdominis muscle
Treatment:
Procedure: TAP block
Control
Sham Comparator group
Description:
A sham band-aid will be applied to the abdomen of subjects who are randomized to the no intervention group.
Treatment:
Procedure: Control

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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