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Compares treatment options for Opioid Use
Official title Evaluation of the Stress Response in Anesthesia Use Inhalation Anesthetic (Desflurane) Versus TIVA for Bariatric Surgery
ClinicalTrials.gov ID: NCT07568938
What this study is testing
What is opioid free anesthesia?
opioid free anesthesia is an investigational medicine, being studied as a potential treatment for opioid use.
Also referred to as Desflurane.
Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.
- What it's testing
- 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?
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 65
You may be able to join if
- Signed Informed Consent
- ASA II-III
- Morbid obesity confirmed diagnosis and approval for surgical treatment
- Laparoscopic sleeve gastrectomy (LSG) or Gastric By pass (R-Y By pass /SASI/SADI AND one anastomosis by pass )
- Preop respiratrory assessment conducted
You likely can't join if
- Patients declining or withdrawing consent
- Patients unsuitabe with regards to compliance to treatment, according to the researcher's assessment
- Bradycardia, AV block, , postural hypotension
- QTcF\>470msec
- Known allergy or hypersensitiity to any of the medications administered
- Stop-BANG score \>6
See the full eligibility criteria
- Signed Informed Consent
- ASA II-III
- Morbid obesity confirmed diagnosis and approval for surgical treatment
- Laparoscopic sleeve gastrectomy (LSG) or Gastric By pass (R-Y By pass /SASI/SADI AND one anastomosis by pass )
- Preop respiratrory assessment conducted
- Adequate organ and bone marrow function
- Patients declining or withdrawing consent
- Patients unsuitabe with regards to compliance to treatment, according to the researcher's assessment
- Bradycardia, AV block, , postural hypotension
- QTcF\>470msec
- Known allergy or hypersensitiity to any of the medications administered
- Stop-BANG score \>6
- Intraoperative administration of more than 8mg of prednisolone or equivalent
- Patients who have received corticosteroids for durations \>3 weeks at any point in their lifetime
- Participation in other clinical trial for experimental product administered post operatively
- Diagnosis of depression
The study team makes the final eligibility decision.
Where it's taking place
- Athens, Greece
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 65 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Athens, Greece. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.