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NCT06515691Recruiting

Modified Thoracoabdominal Nerve Plane Block In Laparoscopic Sleeve Gastrectomy

Evaluation of Effectiveness of Ultrasound-Guided Modified Thoracoabdominal Nerve Plane Block Through Perichondrial Approach (M-TAPA) for Postoperative Analgesia Management in Patients Undergoing Laparoscopic Sleeve Gastrectomy Operation

Source: ClinicalTrials.gov · Last updated 24 Dec 2025

Brief summary (registry, in English)

Ultrasound-guided Modified Thoracoabdominal Nerve Plane Block (M-TAPA) is performed into the costochondral aspect at the 9th-10th costal level by injecting local anesthetics deep into the chondrium. It provides blockage of both the anterior and lateral cutaneous branches of the thoracoabdominal nerve. Studies show that M-TAPA block is effective for postoperative analgesia and other abdominal surgeries, but its effect on patients undergoing LSG surgery has not yet been studied. The hypothesis is that the M-TAPA block performed in patients undergoing Laparoscopic Sleeve Gastrectomy (LSG) Operation would reduce opioid consumption in the first 24 hours period after surgery.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
17 Jul 2024
Start date
3 Jan 2025
Primary completion date
15 Feb 2026
Lead sponsor
Istanbul Medipol University Hospital
Diseases
Obesity
NCT number
NCT06515691

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From 3 Jan 2025 to the primary completion date, 15 Feb 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • receiving anticoagulant treatment,

Other illness

  • with a history of bleeding diathesis,
  • with allergies or sensitivity to drugs used,
  • with an infection on the puncture site
  • with a history of alcohol or drug addiction,
  • with congestive heart failure
  • with liver or kidney disease

Other

  • who do not accept the procedure or participate in the study

Who the study is looking for

  • \-

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Istanbul Medipol University Mega Hospital Complex
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Recruiting

This page is information, not medical advice. Discuss any trial with your doctor.