Skip to main content
UK clinical trials - updated daily from ClinicalTrials.gov
TrialConnect
← Back to Search
Study stopped earlyN/A

Five PLus Year EffIcacy of Endoscopic Sleeve Gastroplasty (ESG) for Sustained WeigHT Loss

Sponsor: Boston Scientific Corporation

NCT ID: NCT06894498

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
No Intervention: Observational Cohort (other)
How long the study runs
Study runs about 4 months (dates as stated)
About the drug or intervention
No Intervention: Observational Cohort — other: No Intervention, Observational Cohort
Patient visit burden
Not specified by the sponsor
Type of study
Observing health over time
Ages
18 Years and over
Who
All
Number of participants
2
Started
2026-03-31
Last checked
2026-08

Plain English Summary

What is this study?

  • • Testing a new treatment for obesity and obesity-related medical conditions
  • • Clinical study - 2 participants
  • • The objective of this study is to assess the long term weight loss and weight loss journey of patients who received an Endoscopic Sleeve Gastroplasty (ESG) 5 or more years prior to enrollment

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with obesity and obesity-related medical conditions

Where?

  • • No UK sites listed for this trial

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

The objective of this study is to assess the long term weight loss and weight loss journey of patients who received an Endoscopic Sleeve Gastroplasty (ESG) 5 or more years prior to enrollment.

More detail

Includes retrospective data collection and one prospective visit

Obesity and Obesity-related Medical ConditionsWeight Loss

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓Subject is ≥ 18 years of age at the time of the ESG procedure
  • ✓Subject with a BMI between 30 kg/m2 and 50 kg/m2, inclusive, at the time of the primary ESG procedure using...
  • ✓Subject completed follow-up 1-year from the ESG procedure for weight loss management
  • ✓Subject completed or is eligible for follow-up 5-years from the ESG procedure for weight loss management (visit can...
  • ✓Subject has returned for a minimum of one annual follow-up at the treating site for weight loss management annually...
See the full criteria
Inclusion Criteria: * Subject is ≥ 18 years of age at the time of the ESG procedure * Subject with a BMI between 30 kg/m2 and 50 kg/m2, inclusive, at the time of the primary ESG procedure using Overstitch Endoscopic Suturing System * Subject completed follow-up 1-year from the ESG procedure for weight loss management * Subject completed or is eligible for follow-up 5-years from the ESG procedure for weight loss management (visit can be collected either retrospectively or prospectively) * Subject has returned for a minimum of one annual follow-up at the treating site for weight loss management annually between two and four years from the procedure. * Subject is willing to complete one prospective visit (5 year or 5+ year, as appropriate) * Subject is able to read, understand, and sign a written Informed Consent Form to participate in the study Exclusion Criteria: * None
Data sourced from ClinicalTrials.gov · Last verified: 2026-08