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NCT06812364Not yet recruiting

Bilateral Thorathic Erector Spinae Plane Block in Laparoscopic Bariatic Surgeries

COMPARISON OF THE EFFICACY OF ONE LEVEL AND TWO LEVEL OF BILATERAL THORACIC ERECTOR SPINAE PLANE BLOCK COMBINED WITH GENERAL ANESTHESIA IN LAPAROSCOPIC BARIATRIC SURGERY FOR OBESE PATIENTS: RANDOMIZED CONTROLLED TRIAL

Source: ClinicalTrials.gov · Last updated 6 Feb 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The study is to evaluate effectiveness of one-level versus two-level thoracic ESP block on intraoperative and postoperative analgesia in bariatric surgeries and to compare total opioid consumption of both groups.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
58 (estimated)
First submitted
1 Feb 2025
Start date
1 Mar 2025
Primary completion date
20 Sept 2025
Lead sponsor
Cairo University
Diseases
Obesity
NCT number
NCT06812364

What you commit to

  • Study type: Observational
  • Planned participants: 58
  • From 1 Mar 2025 to the primary completion date, 20 Sept 2025
  • 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.

Lab values

  • • Refusal of regional block
    • Patients with neurological, psychological disorders or those lacking cooperation.
    • Patients scheduled for concomitant laparoscopic cholecystectomy or paraumbilical hernia repair or those with history of previous bariatric surgery or obstructive sleep apnea.
    • Patients with anatomic abnormalities at site of injection, skin lesions or wounds at site of proposed needle insertion.
    • Patients with bleeding disorders defined as (INR \>1.4) and/ or (platelet count \<100,000/µL)
    • Patients with hepatic disease e.g. liver cell failure or hepatic malignancy or hepatic enlargement.
    • Patients who are allergic to amide local anesthetics

Who the study is looking for

  • Patient age ranges 18 to 60 years old
  • Obese patients ; Body mass index(BMI) ≥ 35 - 50 kg/m2
  • American Society of Anesthesiologists (13) physical status classes II to III
  • Patients scheduled for laparoscopic bariatric surgery i.e. sleeve gastrectomy and/or Roux-en-Y gastric bypass (RYGB) surgeries

Age in the registry: 18 years to 60 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Faculty of Medecine Cairo Uneversity
Coordinator of this site? Confirm its status
CairoEgyptUnknown status

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