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Conversion to SADI-S, RYGB or OAGB After Failed Sleeve

Conversion of Failed Sleeve Gastrectomy Due to Weight Regain to SADI-S, RYGB or OAGB

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05608772
Acronym
RCTresleeve
Enrollment
234
Registered
2022-11-08
Start date
2023-03-15
Completion date
2028-04-15
Last updated
2025-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bariatric Surgery Candidate, Comorbidities and Coexisting Conditions, Nutrient Deficiency, Weight Loss

Keywords

RYGB, OAGB, SADI-S, Sleeve gastrectomy

Brief summary

Assess what revisional surgery is superior and provides the best weight loss after primary LSG. What is the occurrence of complications and the nutritional laboratory status? And if the resolution and /or improvement of associated medical problems after the weight loss will occur.

Detailed description

Laparoscopic sleeve gastrectomy (LSG) gained popularity and has become one of the most performed weight loss procedures worldwide. In the long-term follow-up, the literature states that the incidence of gastroesophageal reflux disease (GERD) accounts for 16%, and weight regains accounting for 70% after LSG. These are the two most common complications which can necessitate further surgical intervention. The hypotheses are that laparoscopic conversion from LSG to Single anastomosis duodeno-ileal bypass (SADI-S), Roux-en-Y gastric bypass (RYGB), or one anastomosis gastric bypass (OAGB) will provide a new significant weight loss, improvement in obesity-related health problems and provide no nutritional deficiency in all cases. Since the three types of procedures have other anatomical presentations, whereby these is not well tested next to each other in a blinded, controlled setting for the patient, this study is designed to discover if the procedures are superior to each other or not and what the best outcome is for the patient. A sample size is calculated and with a medium effect size of 0.5 corresponds to a mean difference in %EBMIL between SADI-S, RYGB, and OAGB of at least 10%. Using a power of 0.8 with an alpha of 0.05 resulted in a sample size of 64 patients per group. Considering a possible loss of patients to follow-up, an additional 20% increase in sample size was included per group, resulting in a minimum of 78 patients per group. (Total of 3 groups together of 234 patients).

Interventions

revision procedure after failed sleeve gastrectomy

Sponsors

General Committee of Teaching Hospitals and Institutes, Egypt
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Intervention model description

A single-blind randomization procedure, in which patients and outpatient clinic nurses will be blinded to the study period p

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Undergone primary laparoscopic sleeve gastrectomy in the past * Weight regain * defined as any increase in weight above the nadir as reported by the patient * BMI at the time of revisional surgery was around 45 kg/m2 * weight regain was defined as an increase in BMI after bariatric surgery to exceed 35 * With or without Gastroesophageal reflux disease (GERD) grade A and B o Patients with grade C or higher GERD, according to the Los Angeles (LA) classification \[7\] will be excluded from the study

Exclusion criteria

* Didn't follow preoperative consultation * Cannot give of sign informed consent

Design outcomes

Primary

MeasureTime frameDescription
The number of participants who will have early complications related to surgery6 weeksthe incidence of re-operation, bleeding or leakages
somscore of food tolerance2,6 weeks and 3,6,12,24 monthsvalidated food tolerance questions: Food tolerance (FT) was evaluated using a one-page questionnaire divided into 4 sections, 3 of which were used to calculate the score: overall patient satisfaction with eating (score: 1-5); tolerability to certain food types (score: 0-16); and frequency of vomiting/regurgitation (score: 0-6), with a total score between 1 and 27; higher scores indicate better food tolerance
The percentage Excess body weight loss (%EWL)3,6,12,24 monthsthe amount of weight loss after revision surgery

Secondary

MeasureTime frameDescription
Nutritional levels of albuminemia3,6,12,24 monthsthe albuminemia level will be tested after surgery (g/dl)
Nutritional levels of proteinemia3,6,12,24 monthsthe proteinemia level will be tested after surgery (mg/dl)
Nutritional levels of anemia3,6,12,24 monthsthe anemia level will be tested after surgery (Mcl)
Nutritional levels of calcemic3,6,12,24 monthsthe calcemic level will be tested after surgery (mg/dl)
Incidence of Reflux3,6,12,24 monthsGERD assessment
The number of participants who will have late complications related to surgery3,6,12,24 monthsthe incidence of re-operations will be collected
Short Form 36 Quality of life3,6,12,24 monthsQuality of life assessment will be tested 8 chapters with in total 36 questions and a somscore from 0-100 will be calculated (the higher the somscore the better the quality of life is).
VAS/NRS (incidence of pain)3,6,12,24 monthspain scoring from 0-10 (0 is no pain 10 is most worst pain)
Metabolic biomarkers Glucagon-like peptide-1 (GLP1)3,6,12,24 monthsthe GLP1 level will be tested after surgery (mg/ml)
Metabolic biomarkers Leptin3,6,12,24 monthsthe Leptin level will be tested after surgery (mg/ml)
Metabolic biomarkers Peptide YY ( PYY)3,6,12,24 monthsthe PYY level will be tested after surgery (pg/ml)
Metabolic biomarkers Ghrelin3,6,12,24 monthsthe Ghrelin level will be tested after surgery (mg/ml)
Metabolic biomarkers Insulin3,6,12,24 monthsthe Insulin level will be tested after surgery (million units/ml)

Other

MeasureTime frameDescription
The number of participants who will have late complications related to surgery60 monthsthe incidence of re-operations or complications will be collected
Incidence of Reflux60 monthsGERD classification
The percentage Excess body weight loss (%EWL)60 monthsthe amount of weight loss after revision surgery
The number of participants whereby revision surgery necessary after the RCT60 monthsthe incidence of re-operations or other procedure will be collected
Nutritional levels of albuminemia60 monthsthe albuminemia level will be tested after surgery (g/dl)
Nutritional levels of proteinemia60 monthsthe proteinemia level will be tested after surgery (mg/dl)
Nutritional levels of anemia60 monthsthe anemia level will be tested after surgery (Mcl)
Nutritional levels of calcemic60 monthsthe calcemic level will be tested after surgery (mg/dl)
Somscore of food tolerance60 monthsvalidated food tolerance questions: Food tolerance (FT) was evaluated using a one-page questionnaire divided into 4 sections, 3 of which were used to calculate the score: overall patient satisfaction with eating (score: 1-5); tolerability to certain food types (score: 0-16); and frequency of vomiting/regurgitation (score: 0-6), with a total score between 1 and 27; higher scores indicate better food tolerance
Short Form 36 Quality of life60 monthsQuality of life assessment will be tested 8 chapters with in total 36 questions and a somscore from 0-100 will be calculated (the higher the somscore the better the quality of life is).
VAS/NRS (incidence of pain)60 monthspain scoring from 0-10 (0 is no pain 10 is most worst pain)
Metabolic biomarkers Glucagon-like peptide-1 (GLP1)60 monthsthe GLP1 level will be tested after surgery (mg/ml)
Metabolic biomarkers Leptin60 monthsthe Leptin level will be tested after surgery (mg/ml)
Metabolic biomarkers Peptide YY ( PYY)60 monthsthe PYY level will be tested after surgery (pg/ml)
Metabolic biomarkers Ghrelin60 monthsthe Ghrelin level will be tested after surgery (mg/ml)
Metabolic biomarkers Insulin60 monthsthe Insulin level will be tested after surgery (million units/ml)

Countries

Egypt

Contacts

Primary ContactBart Torensma, PHD
bart@torensmaresearch.nl+31641389070
Backup ContactMohamed Ashour, MD
mohamed.ashour@alexu.edu.eg+201002600970

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026