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BEST: Bypass equipoise sleeve trial; rationale and design of a randomized, registry-based, multicenter trial comparing Roux-en-Y gastric bypass with sleeve gastrectomy
Univ Gothenburg, Sweden; Sahlgrens Univ Hosp, Sweden.
Linköpings universitet, Institutionen för klinisk och experimentell medicin, Avdelningen för Kirurgi, Ortopedi och Onkologi. Linköpings universitet, Medicinska fakulteten. Region Östergötland, Centrum för kirurgi, ortopedi och cancervård, Kirurgiska kliniken ViN.ORCID-id: 0000-0002-7218-3390
Natl Inst Hlth and Welf, Finland.
Mora Hosp, Sweden; Karolinska Inst, Sweden.
Vise andre og tillknytning
2019 (engelsk)Inngår i: Contemporary Clinical Trials, ISSN 1551-7144, E-ISSN 1559-2030, Vol. 84, artikkel-id 105809Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Background

Laparoscopic gastric bypass (LGBP) is a well-documented surgical intervention for severe obesity. Recently, laparoscopic sleeve gastrectomy (LSG) has gained increased popularity. Short-term follow-up in limited-sized randomized trials comparing LGBP and LSG show no major differences in weight-loss, adverse events, or effect on comorbidities; however, there is a lack of sufficiently powered, pragmatic, randomized controlled trials comparing the mid- and long-term results of the two methods.

Method

BEST is a randomized, registry-based, multicenter trial comparing LGBP and LSG. The trial has two primary outcomes; rates of substantial complications (SC) and total body weight loss. We hypothesize that patients treated with LSG will experience 35% fewer substantial complications during the 5-year follow-up compared to patients treated with LGBP, and that the efficacy of LSG will remain within a non-inferiority margin of 5% in terms of weight loss. Our sample size calculation, using data from the Scandinavian Obesity Surgery Registry (SOReg), shows a power of 80% for SC and > 95% for weight loss at p < .025 with a total of 2100 included patients.

The design of the trial will also enable comparisons within several relevant patient subgroups.

Conclusions

As a large-sized, pragmatic, randomized trial, BEST will provide robust data comparing LGBP with LSG by generating long-term results on weight loss and SC's, as well as secondary outcomes and comparisons within patient subgroups. The use of a well-established registry for registration of all data facilitates a large multicenter trial, and combines the strengths of registry studies with those of a randomized trial.

Clinical Trials registry: NCT 02767505.

sted, utgiver, år, opplag, sider
Elsevier, 2019. Vol. 84, artikkel-id 105809
Emneord [en]
Laparoscopic gastric bypass; Laparoscopic sleeve gastrectomy; Randomized clinical trial; Registry study
HSV kategori
Identifikatorer
URN: urn:nbn:se:liu:diva-161416DOI: 10.1016/j.cct.2019.07.001ISI: 000488654600008PubMedID: 31279778OAI: oai:DiVA.org:liu-161416DiVA, id: diva2:1367039
Merknad

Funding Agencies|Swedish Research CouncilSwedish Research Council; Erling Persson Family Foundation; ALF Vastra G8taland region

Tilgjengelig fra: 2019-10-31 Laget: 2019-10-31 Sist oppdatert: 2021-12-29bibliografisk kontrollert

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