← Eichor
Study identifier: NCT06778629 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Transversalis Fascia Plane Block for Laparoscopic Inguinal Hernia Repair

Condition: Laparoscopic Inguinal Hernia Repair · Acute Post Operative Pain  ·  Sponsor: Istanbul Medipol University Hospital

PhaseNA
Planned participants60
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

Transversalis Fascia Plane Block (TFPB) is a trunk block that blocks the T12- L2 spinal nerves by injection of local anesthetic between the transversus abdominis muscle and transversalis fascia on the lateral abdominal wall. The block's positive effects on postoperative analgesia have been shown in many abdominal surgeries, including open-technique inguinal hernia repair. This study aimed to investigate the effectiveness of ultrasound (US) guided TFPB on postoperative pain control for postoperative analgesia management after laparoscopic inguinal hernia repair.

This description comes directly from the study's public registry record.

Talk to the study team

AYSE INCE, Assist Prof  ·  +90 5366774988  ·  drayseince@gmail.com

HANDE GUNGOR DANISAN, Assist Prof  ·  +90 5053478392  ·  drhandegungor@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Istanbul Medipol University Mega Hospital ComplexIstanbul, Bagcilar, Turkey (Türkiye)Recruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06778629