Evaluation of the Effectiveness of Transversalis Fascia Plane Block in Patients Undergoing Laparoscopic Inguinal Hernia Repair

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• American Society of Anesthesiologists (ASA) classification I- II Patients

• Unilateral Inguinal Hernia Repair Surgery

• Elective Operations

Locations
Other Locations
Turkey
Istanbul Medipol University Mega Hospital Complex
RECRUITING
Istanbul
Contact Information
Primary
AYSE INCE, Assist Prof
drayseince@gmail.com
+90 5366774988
Backup
HANDE GUNGOR DANISAN, Assist Prof
drhandegungor@gmail.com
+90 5053478392
Time Frame
Start Date: 2025-02-14
Estimated Completion Date: 2025-12-15
Participants
Target number of participants: 60
Treatments
Experimental: Group T = TFPB group
Transversalis Fascia Plane block will be performed. Local anesthetic infiltration to port entrance sites at the beginning of the operation and standard postoperative pain management protocols will be applied.
Active_comparator: Group K = Control group
Local anesthetic infiltration to port entrance sites at the beginning of the operation and standard postoperative pain management protocols will be applied. No plane block will be applied.
Related Therapeutic Areas
Sponsors
Leads: Istanbul Medipol University Hospital

This content was sourced from clinicaltrials.gov