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Clinical Trial NCT07319390 for Bariatric Sleeve Gastrectomy is active, not recruiting. See the Trial Radar Card View and AI discovery tools for all the details. Or ask anything here.
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Midpoint Transverse Process to Pleura Block vs Erector Spinae Plane Block for Postoperative Analgesia in Laparoscopic Sleeve Gastrectomy 52

Active, not recruiting
Clinical Trial NCT07319390 is an interventional study for Bariatric Sleeve Gastrectomy that is active, not recruiting. It started on October 3, 2025 with plans to enroll 52 participants. Led by Ain Shams University, it is expected to complete by March 12, 2026. The latest data from ClinicalTrials.gov was last updated on January 6, 2026.
Brief Summary
The aim of this study will be to compare between MTP and ESPB in terms of postoperative pain score in patients undergoing laparoscopic sleeve gastrectomy
Official Title

Midpoint Transverse Process to Pleura Block vs Erector Spinae Plane Block for Postoperative Analgesia in Laparoscopic Sleeve Gastrectomy

Conditions
Bariatric Sleeve Gastrectomy
Other Study IDs
  • FMASU R226/2025
NCT ID Number
NCT07319390
Start Date (Actual)
2025-10-03
Last Update Posted
2026-01-06
Completion Date (Estimated)
2026-03-12
Enrollment (Estimated)
52
Study Type
Interventional
PHASE
N/A
Status
Active, not recruiting
Primary Purpose
Other
Design Allocation
Randomized
Interventional Model
Parallel
Masking
Single
Arms / Interventions
Participant Group/ArmIntervention/Treatment
Active ComparatorGroup A (ESPB): Bilateral ESP
block at T7 with 20 mL of 0.25% bupivacaine on each side
Erector Spinae Plane Block (ESPB) group
will receive ESPB volume of 20 mls bupivacaine 0.25 % at level T7 bilaterally
Active ComparatorGroup B (MTPB): Bilateral MTP
block at T7 with 20 mL of 0.25% bupivacaine on each side
Midpoint Transverse Process to Pleura Block (MTPPB)
will receive MTPB volume of 20 mls bupivacaine 0.25 % at level T7 bilaterally
Primary Outcome Measures
Outcome MeasureMeasure DescriptionTime Frame
Mean postoperative pain numeric rating scale
Abdominal pain will be assessed using numeric rating scale which includes 10 degrees of which zero is no pain and 10 is maximum pain ever
pain will be evaluated first in postanesthesia care unit then at 1, 3, 6, 8, 12, 18, 24 hours posoperative
Participation Assistant
Eligibility Criteria

Eligible Ages
Adult
Minimum Age
18 Years
Eligible Sexes
All
  • Anesthesiologists (ASA) physical status II, of either sex Age ≥18 y.
  • Undergoing laparoscopic sleeve gastrectomy
  • BMI≥ 35

  • Patient refusal to give consent for the block
  • Hypersensitivity to any of study medications
  • Infection at site of the block
  • Coagulopathy
  • severe cardiac/hepatic/renal disease
Ain Shams University logoAin Shams University344 active studies to explore
No contact data.
2 Study Locations in 1 Countries
Ain Shams University hospitals, Cairo, 11591, Egypt
Ain Shams university hospitals, Cairo, 1234, Egypt