Clinical Trials Directory

Trials / Completed

CompletedNCT02914028

TAP Block and Subacute Pain in Inguinal Herniography

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
2 (actual)
Sponsor
Istanbul University · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
PROCEDUREtransversus abdominis plane blockA peripheric block needle is inserted entering the facia between musculus rectus abdominis and musculus transversus abdominis with ultrasonography and local anesthetics are injected in the facia.
DRUGTramadol and paracetamolTramadol 100 mg and paracetamol 1000 mg are applied to the patients at the end of the surgery

Timeline

Start date
2016-04-01
Primary completion
2016-08-01
Completion
2016-08-01
First posted
2016-09-26
Last updated
2019-02-27

Source: ClinicalTrials.gov record NCT02914028. Inclusion in this directory is not an endorsement.