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Endoscopic stomach procedure for obesity in kidney transplant candidates

Tests an endoscopic stomach-shaping procedure in adults with obesity awaiting kidney transplant.

Plain-language title generated from the registry record
Registry title: Endoscopic Sleeve Gastroplasty With Endomina® for the Treatment of Obesity in Kidney Transplant Candidates

Key facts

Where
Rome, ItalySee the site

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults aged 18 to 70 with a BMI of 35 kg/m² or more and serious kidney disease who need a kidney transplant but are not on the waiting list because of their weight.

Age
18 to 70 years
Sex
All sexes
Disease stage
Chronic kidney disease stage G4-G5 (GFR below 30 ml/min/1.73 m2), expected to reach end-stage kidney disease 6 to 12 months before dialysis would start, or already on haemodialysis, medically stable, with kidney failure judged irreversible.
Earlier treatment
Not listed for transplant because of a high BMI (the transplant centre's cut-off is 35 kg/m2). Anticoagulant or anti-platelet treatment that cannot be stopped is not allowed, except low-dose aspirin (100 mg or less).
Biomarker or test result
BMI of 35 kg/m² or more.

Main reasons for not taking part

  • On peritoneal dialysis
  • Upper gastro-intestinal bleeding in the previous six months
  • Active cancer in the last 5 years
  • Heart attack in the past 6 months, or heart failure class III or IV
  • Previous stomach, oesophagus or duodenum surgery

Read by machine on 12 November 2026.

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 70 years old?

Source: NCT05917795, who can take part

Where in Italy

  • Fondazione Policlinico Universitario A. Gemelli IRCCSRome, ItalyContact: Ivo BoskoskiTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Trial code
NCT05917795
Record updated
28 February 2024
Original description
The aim of this pilot prospective interventional study is to evaluate the efficacy of endoscopic sleeve gastroplasty (ESG) in allowing obese subjects (≥35 kg/m2) with end stage renal disease who need of kidney transplantation to reduce their BMI below 35 in order to be inserted in the waiting list BMI. The main question[s] it aims to answer are:Read full original descriptionShow less

Prospective Pilot Study for the Evaluation of Endoscopic Sleeve Gastroplasty With Endomina® for the Treatment of Obesity in Kidney Transplant Candidates

The aim of this pilot prospective interventional study is to evaluate the efficacy of endoscopic sleeve gastroplasty (ESG) in allowing obese subjects (≥35 kg/m2) with end stage renal disease who need of kidney transplantation to reduce their BMI below 35 in order to be inserted in the waiting list BMI. The main question[s] it aims to answer are:

Is the procedure effective in reducing BMI to the target level in 12 months? Which is the effect on weight loss, quality of life and obesity-related comorbidities? Participants will undergo ESG as per standard clinical practice and followed up to 12 months before transplantation and for 12 months after transplantation.

Inclusion: Adult patients (i.e., age between 18 and 70 years); BMI ≥ 35 kg/m²; Patients with chronic kidney disease (CKD) G4-G5 (glomerular filtration rate [GFR] <30ml/min/1.73 m2) who are expected to reach end-stage kidney disease (ESKD) at least 6 to 12 months before anticipated dialysis initiation (pre-emptive transplant candidates) or patients already on haemodialysis when medically stable and kidney failure deemed irreversible; Patients not listed because of a high BMI according to the policy of the transplant Centre (cut-off 35 kg/m2); Signed informed consent.

Exclusion: Upper gastro-intestinal bleeding (gastric or oesophageal) in the previous six months; Previous stomach, oesophagus or duodenum surgery; Active drugs or alcohol abuse; Ongoing or active malignancy during the last 5 years; Myocardial infarction during the past 6 months or/and heart failure class III or IV according to the New York Heart association's classification; Clinical signs of active infection; Other conditions to exclude the subject in investigators opinion; Concomitant unstoppable anticoagulant or anti platelet therapy, except for low dose aspirin (≤ 100 mg); Patients on peritoneal dialysis; Technical non-feasibility in the opinion of the endoscopist; Pregnancy, lactation (desire to become pregnant during study duration); Enrolment in other clinical studies; Contraindication to general anaesthesia; Refusal to sign informed consent. -.

ClinicalTrials.gov NCT05917795