Evaluating Ultrasound-Guided Modified Thoracoabdominal Nerve Plane Block M-TAPA for Pain Relief After Laparoscopic Sleeve Gastrectomy Surgery
Led by Istanbul Medipol University Hospital · Updated on 2025-12-24
60
Participants Needed
1
Research Sites
N/A
Total Duration
AI-Summary
What this Trial Is About
Researchers are evaluating the effectiveness of the Ultrasound-guided Modified Thoracoabdominal Nerve Plane Block M-TAPA for managing postoperative pain in patients undergoing Laparoscopic Sleeve Gastrectomy LSG, a common bariatric surgery. The study focuses on whether M-TAPA can reduce opioid use within the first 24 hours after surgery, which is important since opioids can cause complications like breathing problems, nausea, and delayed recovery. This research is led by Istanbul Medipol University Hospital and aims to improve pain management and recovery in this patient group.
The study compares two groups one receiving the M-TAPA block along with standard postoperative pain care, and the other receiving only the standard pain management without the nerve block. The M-TAPA procedure involves ultrasound guidance to inject local anesthetic near the ribs to block specific nerve branches. Pain medications including ibuprofen, tramadol, and fentanyl via a patient-controlled system are used in both groups. The M-TAPA block is performed after surgery while the patient is still under general anesthesia.
Participants will be monitored for opioid consumption and pain levels at multiple time points within 24 hours after surgery. Rescue pain medication use and any adverse events during this period will also be recorded. The study uses randomized, double-blind methods to compare outcomes. The total participation includes the surgery, treatment, and close monitoring for the first day after the operation to assess pain relief and medication needs.
CONDITIONS
Brief Title
Modified Thoracoabdominal Nerve Plane Block In Laparoscopic Sleeve Gastrectomy
Research Team
A
ayşe ince, assist pof
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American Society of Anesthesiologists (ASA) classification II-III
Scheduled for laparoscopic sleeve gastrectomy under general anesthesia
You will not qualify if you...
History of bleeding diathesis
Receiving anticoagulant treatment
Allergies or sensitivity to drugs used in the study
Infection at the puncture site
History of alcohol or drug addiction
Congestive heart failure
Liver or kidney disease
Declines to participate or does not accept the procedure
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Treatment
Duration - Day of surgery and 24 hours after surgery
Participants undergo laparoscopic sleeve gastrectomy under general anesthesia. For those in the experimental group, the M-TAPA block is performed after wound closure while still under anesthesia. All participants receive standard postoperative pain management, including medications and a patient-controlled analgesia system.
1 surgical visit and monitoring during the first 24 hours postoperatively
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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