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Prospective Multicentre Study Assessing the Feasibility of Enhanced Recovery After Sleeve Gastrectomy for Obesity

Prospective Multicentre Study Assessing the Feasibility of Enhanced Recovery After Sleeve Gastrectomy for Obesity

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02042365
Acronym
SLEEVERAS
Enrollment
150
Registered
2014-01-22
Start date
2014-02-28
Completion date
2014-12-31
Last updated
2014-02-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Keywords

Enhanced recovery,, sleeve gastrectomy,

Brief summary

The primary purpose of the study is to test the feasibility of a protocol of enhanced recovery after surgery for reducing the total length of hospital stay in a large scale setting

Detailed description

This observational study evaluates the feasibility of ERAS pathway in six French departments of surgery located at Clermont-Ferrand, Bordeaux, Montpellier, Amiens, Strasbourg and Aurillac.

Interventions

PROCEDUREERAS (Enhanced recovery after surgery)

Sponsors

Direction Générale de l'Offre de Soins
CollaboratorOTHER_GOV
Ministry of Health, France
CollaboratorOTHER_GOV
University Hospital, Clermont-Ferrand
Lead SponsorOTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Obese patients undergoing a sleeve gastrectomy Patients having signed the informed consent Patients over 18 year old ASA 1-3 Obesity with indication for surgery according the guidelines of the French High Authority for Health BMI \< 50 kg/m2 No contra-indication for general anesthésia

Exclusion criteria

contra-indication for general anesthésia Age under 18 years ASA 4 BMI \> 50 kg/m2 Patients having other serious comorbidities: cardiac, pulmonary, diabete, immunodepression, coagulopathy ou anticoagulant therapy Pregnancy Patients living alone

Design outcomes

Primary

MeasureTime frameDescription
Duration of hospital stayat day 1Posoperative day when the patients satisfies the criteria of discharge

Countries

France

Contacts

Primary ContactPatrick LACARIN
placarin@chu-clermontferrand.fr04 73 75 11 95

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026