Opioid-free anesthesia for bariatric surgery
Non-opioid Anesthesia in Bariatric Surgery
This study looks at whether using opioid-free anesthesia during bariatric surgery can help patients recover better and manage pain after the surgery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital, Strasbourg, France Academic / other |
| Locations | 1 site (Strasbourg) |
| Trial ID | NCT06162416 on ClinicalTrials.gov |
What this trial studies
This observational study investigates the use of opioid-free anesthesia in patients undergoing bariatric surgery. It aims to evaluate the potential benefits of reducing morphine use during surgery, particularly in terms of postoperative pain management and rehabilitation outcomes. The study will analyze data from patients who had bariatric surgery at the University Hospital of Strasbourg between 2017 and 2019. By examining the effects of this anesthesia approach, the study seeks to clarify its role in improving recovery for obese patients.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who have undergone bariatric surgery at the University Hospital of Strasbourg between January 2017 and December 2019.
Not a fit: Patients who are under guardianship, pregnant, or have opted out of participating in the study will not benefit.
Why it matters
Potential benefit: If successful, this approach could enhance postoperative recovery and reduce side effects associated with opioid use in bariatric surgery patients.
How similar studies have performed: While the concept of opioid-free anesthesia has been explored, this specific application in bariatric surgery is still being evaluated and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion criteria: * Major subject (≥ 18 years old), * who have undergone bariatric surgery at the HUS between January 01, 2017 and December 31, 2019 * Subject who has not expressed his or her opposition, after information, to the reuse of his or her data for the purpose of this research Exclusion Criteria: * Subject who has expressed his/her opposition to participate in the study * Subjects under guardianship, curatorship or legal protection, pregnant women
Where this trial is running
Strasbourg
- Service de Réanimation Chirurgicale - CHU de Strasbourg - France — Strasbourg, France (Recruiting)
Study contacts
- Study coordinator: Antoine PONS, MD
- Email: antoine.pons@chru-strasbourg.fr
- Phone: 33 3 69 55 00 84
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.