Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT07568938

Evaluation of the Stress Response in Anesthesia Use Inhalation Anesthetic (Desflurane) Versus TIVA for Bariatric Surgery

Led by G.Gennimatas General Hospital · Updated on 2026-05-06

70

Participants Needed

1

Research Sites

176 weeks

Total Duration

On this page

Sponsors

G

G.Gennimatas General Hospital

Lead Sponsor

N

National and Kapodistrian University of Athens

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to compare the effects of Opioid Free Anesthesia (OFA) with and without volatile anesthetics (in this case desflurane) in patients undergoing bariatric surgery. The main question it aims to answer : -Will there be a difference in the perioperative stress between patients receiving OFA with and without desflurane? Participants will undergoing sleeve gastrectomy or gastric by pass, will be administered OFA with and without desflurane and blood tests (cortisole, ACTH,dopamine, PRL, adrenaline, noradrenaline, lactate) will be collected perioperatively to compare stress in the two groups.

CONDITIONS

Official Title

Evaluation of the Stress Response in Anesthesia Use Inhalation Anesthetic (Desflurane) Versus TIVA for Bariatric Surgery

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Signed Informed Consent
  • ASA physical status II or III
  • Confirmed diagnosis of morbid obesity with approval for surgical treatment
  • Scheduled for laparoscopic sleeve gastrectomy or gastric bypass surgery (R-Y bypass, SASI, SADI, or one anastomosis bypass)
  • Preoperative respiratory assessment completed
  • Adequate organ and bone marrow function
Not Eligible

You will not qualify if you...

  • Declining or withdrawing consent
  • Unsuitable for treatment compliance as assessed by the researcher
  • Bradycardia, AV block, or postural hypotension
  • QTcF greater than 470 msec
  • Known allergy or hypersensitivity to any administered medications
  • Stop-BANG score greater than 6
  • Intraoperative use of more than 8 mg prednisolone or equivalent
  • History of corticosteroid use for more than 3 weeks at any time
  • Participation in another clinical trial involving experimental post-operative products
  • Diagnosis of depression

AI-Screening

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Trial Site Locations

Total: 1 location

1

General Hospital of Athens G. Gennimatas

Athens, Greece, 11527

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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