Ireland
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Recruiting Not applicable

M-Tapa Block and Transversus Abdominal Plane Block for Postoperative Analgesia in Unilateral Open Inguinal Hernia Repair Surgery

NCT07311902 · tracked via the Priya Life Science Turkey tracker
Sponsor
Erzurum Regional Training & Research Hospital
Phase
Not applicable
Started
2024-11-01
Last updated
2025-12-31

Condition(s) studied

Pain ManagementMtapa BlockTAP Block

Investigational drug(s) / intervention(s)

TAP Block GroupM TAPA block

TAP Block Group: 20 ml of 0.25% bupivacaine

M TAPA block: 20 ml of 0.25% bupivacaine

Study summary

Patients will be called to the operating room one hour before surgery and no premedication will be applied before coming to the operating room. Patients in both groups who are taken to the block room will be administered 1-2 mg iv midazolam for sedation. M TAPA block will be applied for the surgical procedure. After aseptic conditions are provided, the high-frequency linear US probe will be covered with a sterile sheath. The US probe will be placed in the saggital plane at the costochondral angle where the midclavicular line intersects the costal cartilage. 5 ml of saline will be injected using the in-plane technique using a 22G 100 mm block needle and the block location will be verified. After the block location is verified, a total of 20 ml of 0.25% bupivacaine will be injected unilaterally and the procedure will be terminated. After aseptic conditions are provided, the high-frequency linear US probe will be covered with a sterile sheath. In TAP block, the block needle will be advanced to the fascial plane between the internal oblique and transversus abdominis muscles with the in-plane technique and the procedure will be completed by injecting 5 ml 20 ml 0.25% bupivacaine unilaterally. The same analgesia protocol will be applied to both groups intraoperatively and postoperatively, and a survey will be conducted on the patients at the 24th hour postoperatively.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Exclusion Criteria: * History of bleeding diathesis * Allergy or sensitivity to local anesthetics and opioids * Infection in the area where the block will be applied * Alcohol or drug addiction * Patients with a BMI \> 30 * Suspected pregnancy * Women in pregnancy or lactation * Patients with allergies to study drugs * Patient refusal * Use of anticoagulant agents Inclusion Criteria: * Planning for elective unilateral open inguinal hernia repair surgery * ASA I-II status * Being between 18 and 65 years of age

Primary outcome measure(s)

  • pain score — The primary aim of our study was to compare VAS scores at 1, 2, 4, 8, 12, and 24 hours postoperatively and to evaluate the level of comfort.
    Patients' pain scores will be evaluated

Trial sites (1)

FacilityCityRegionStatus
Erzurum Regional Education and Research Hospital Erzurum Turkey (Türkiye) Recruiting

More Erzurum Regional Training & Research Hospital trials in Turkey

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07311902 on ClinicalTrials.gov ↗ ← All trials in Turkey