Procedure for Duodenal-Ileal Diversion for Patients With Weight Regain Following Sleeve Gastrectomy (NCT05049824) | Clinical Trial Compass
CompletedNot Applicable
Procedure for Duodenal-Ileal Diversion for Patients With Weight Regain Following Sleeve Gastrectomy
Spain27 participantsStarted 2021-10-26
Plain-language summary
Study will monitor weight loss and metabolic indicators for subjects in single-center, single arm trial.
Who can participate
Age range19 Years – 65 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Age 22-65 years at screening
* Body mass index (BMI) ≥35 and ≤50
* Patient is ≥12 months but ≤ 60 months post sleeve gastrectomy who have inadequate weight loss or weight regain.
* Weight stable over 3-month period
* Negative H. pylori breath test
* Agrees to refrain from any type of additional bariatric or reconstructive surgery that would affect body weight for a duration of 2 years
* If female, subject must commit to not becoming pregnant for 24 months and agree to use contraception during this period
* Able to understand and sign informed consent documents.
Exclusion Criteria:
* Known or suspected allergy to nickel or titanium or nitinol
* Contraindication to general anesthesia
* Previous technical difficulty or failed endoscopy or contraindication to endoscopy of upper GI series
* Any previous major surgery on the stomach (excluding sleeve gastrectomy), duodenum, hepatobiliary tree (excluding gallbladder), pancreas, or right colon.
* Clinically significant findings during screening endoscopy at target region for compression anastomosis
* Uncontrolled hypertension
* Pre-existing severe comorbid cardio-respiratory disease
* History of type 1 diabetes or poorly controlled type 2 diabetes
* Abnormal liver biochemistry
* History of chronic gastrointestinal disease
* Specific genetic or hormonal cause of obesity
* Recent tobacco/nicotine product cessation (within 3 months prior)