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Clinical Trials/NCT02914028
NCT02914028
Completed
Not Applicable

Evaluation of the Effects of Subcostal Transversus Abdominis Plane Block on Subacute Pain Development Following Inguinal Herniography: a Randomized Clinical Study

Istanbul University0 sites2 target enrollmentApril 2016

Overview

Phase
Not Applicable
Intervention
Tramadol and paracetamol
Conditions
Postoperative Pain
Sponsor
Istanbul University
Enrollment
2
Primary Endpoint
verbal numeric scale
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Inguinal hernia repair with mesh has a high incidence of postoperative chronic pain. Transversus abdominis plane block is a current intervention to support postoperative analgesia, however it is recently in research area how to be applied in different surgical areas to be more effective than intravenous opioids. Subcostal transversus abdominis plane block is not advised but has not been studied to be effective for postoperative analgesia in inguinal herniography patients.

This study aims to research the effect of subcostal transversus abdominis plane block in subacute postoperative pain after inguinal hernia repair

Detailed Description

Patients were divided into two groups, one is control and the second is subcostal transversus abdominis plane block (STAP) group. After standard general anesthesia application, control group ( Group I) had 1 gram of paracetamol and 100 mg of contramal just after starting surgical closure. Group II (STAP) had 1 gram of paracetamol and 100 mg of contramal, after surgical closure transversus abdominis plane block in subcostal area was applied to the patient.

Registry
clinicaltrials.gov
Start Date
April 2016
End Date
August 2016
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dr Cigdem Akyol Beyoğlu

medical doctor

Istanbul University

Eligibility Criteria

Inclusion Criteria

  • ASA I-III
  • who were to undergo elective unilateral inguinal herniography with "mesh" under general anesthesia.

Exclusion Criteria

  • patients who have allergy to local anesthetics

Arms & Interventions

Tramadol and paracetamol

subjects were administered intravenous analgesia (control group) Tramadol 100 mg and paracetamol 1000 mg at the end of the surgery

Intervention: Tramadol and paracetamol

transversus abdominis plane block

patients that applied transversus abdominis plane block at the end of the surgery after given intravenous analgesia

Intervention: transversus abdominis plane block

transversus abdominis plane block

patients that applied transversus abdominis plane block at the end of the surgery after given intravenous analgesia

Intervention: Tramadol and paracetamol

Outcomes

Primary Outcomes

verbal numeric scale

Time Frame: 1 month after the operation

patients were questioned for pain graduation to give a point from 0 to 10 according to the intensity of the pain. 0 equals to no pain, 10 equals to the strongest pain

Secondary Outcomes

  • verbal numeric scale(15 minutes, 1-6-12-24 hours and 15 days after operation)

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