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NCT06162416 Clinical Trial

Non-opioid Anesthesia in Bariatric Surgery

Severe Obesity Clinical Trial

— BARIA  

Official title:
Non-opioid Anesthesia in Bariatric Surgery

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT06162416
Other study ID # 7645
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 11, 2020
Est. completion date December 31, 2023

Study information
Verified date December 2023
Source University Hospital, Strasbourg, France
Contact Antoine PONS, MD
Phone 33 3 69 55 00 84
Email antoine.pons@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Opioid-free anesthesia is a new approach to anesthesia, described and used for many years. If it represents many advantages by reducing the side effects of morphine, its precise place in current practice and in terms of postoperative rehabilitation remains to be determined. Studies are not yet numerous enough to affirm a real benefit. Obese patients are potentially able to benefit from the reduction in the use of morphine during surgery, in terms of quality of postoperative analgesia, side effects (respiratory depression, ileus, somnolence) and early rehabilitation.

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date December 31, 2023
Est. primary completion date December 2023
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility 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

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France Service de Réanimation Chirurgicale - CHU de Strasbourg - France Strasbourg

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Dose of morphine used intraoperatively Intraoperative (during the operation)
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