A UK Registry for Metabolic and Bariatric Endoscopic Interventions
NCT ID: NCT06305208
Last Updated: 2024-03-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
300 participants
OBSERVATIONAL
2024-02-01
2039-02-01
Brief Summary
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Detailed Description
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The objective of this registry is to collect demographic, procedural and follow-up outcome data on the use of metabolic and bariatric endoscopic procedures in patients with obesity and/or obesity-related complications. This registry will provide real-life outcomes on the use of these novel endoscopic devices from multiple centres participating across the UK to provide longer-term safety and efficacy data. In addition, the registry will enable development of a UK-wide research network to support further research, innovation, and training into metabolic and bariatric endoscopy.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Primary bariatric endoscopic procedures
Endoscopic gastric suturing
Endoscopic suturing of the stomach to reduce volume and promote weight loss with either the Apollo Overstitch or Overstitch Sx system.
Endoscopic gastric plication
Endoscopic plication of the stomach to reduce volume and promote weight loss with either the POSE or Endomina system.
Intragastric balloon(s)
The insertion of an intragastric implant into the stomach, which is subsequently filled with air or water to promote weight loss. Several intragastric balloons are available including Allurion, Heliosphere, Obalon, Orbera, and Spatz.
Revisional bariatric endoscopic procedures
Revisional gastroplasty
Endoscopic suturing or plication of the stomach among patients who have previously undergone gastroplasty, sleeve gastrectomy, or Roux-en-Y gastric bypass to restrict the stomach and promote weight loss
Transoral outlet reduction endoscopy (TORe)
Reduction of the size of the gastro-jejunal anastomosis among patients who have previously undergone Roux-en-Y gastric bypass to promote weight loss. A variety of techniques may be used alone or in isolation including suturing (Apollo Overstitch), plication (POSE), argon photocoagulation, and endoscopic submucosal resection/dissection.
Primary metabolic endoscopic procedures
Duodenal mucosal resurfacing (DMR)
Endoscopic ablation of the post-ampullary duodenal mucosal to enhance improvement in glycaemic control among patients with type 2 diabetes.
Interventions
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Endoscopic gastric suturing
Endoscopic suturing of the stomach to reduce volume and promote weight loss with either the Apollo Overstitch or Overstitch Sx system.
Endoscopic gastric plication
Endoscopic plication of the stomach to reduce volume and promote weight loss with either the POSE or Endomina system.
Revisional gastroplasty
Endoscopic suturing or plication of the stomach among patients who have previously undergone gastroplasty, sleeve gastrectomy, or Roux-en-Y gastric bypass to restrict the stomach and promote weight loss
Transoral outlet reduction endoscopy (TORe)
Reduction of the size of the gastro-jejunal anastomosis among patients who have previously undergone Roux-en-Y gastric bypass to promote weight loss. A variety of techniques may be used alone or in isolation including suturing (Apollo Overstitch), plication (POSE), argon photocoagulation, and endoscopic submucosal resection/dissection.
Duodenal mucosal resurfacing (DMR)
Endoscopic ablation of the post-ampullary duodenal mucosal to enhance improvement in glycaemic control among patients with type 2 diabetes.
Intragastric balloon(s)
The insertion of an intragastric implant into the stomach, which is subsequently filled with air or water to promote weight loss. Several intragastric balloons are available including Allurion, Heliosphere, Obalon, Orbera, and Spatz.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Age ≥ 18 years old
* Able to give written informed consent.
Exclusion Criteria
* Any bariatric or metabolic endoscopic procedure not currently listed within the registry protocol or agreed by the steering committee.
* Unable to provide written informed consent.
18 Years
99 Years
ALL
No
Sponsors
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Cleveland Clinic London
OTHER
Responsible Party
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Principal Investigators
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Rehan Haidry, MD
Role: PRINCIPAL_INVESTIGATOR
Cleveland Clinic London
Locations
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Cleveland Clinic London
London, , United Kingdom
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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CCLR-23-018
Identifier Type: -
Identifier Source: org_study_id
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