Ziekenhuisgroep Twente
Almelo, Netherlands
Location status: Recruiting
Location contact
Marc J van Det, MD PhD
CONTACT
Maureen W Tissik, MD
CONTACT
NCT Number: NCT05472922
Rationale: Investigate if there is a significant weight reduction expressed in total body weight loss percentage (%TBWL) in patients 5 years after surgery, whom underwent a mini gastric bypass (MGB-OAGB) with addition of the implantation of a MiniMizer Ring.
Study design: A prospective non blinded single centre randomized controlled trial.
Sudy population: The study population will exist of patients eligible for MGB-OAGB surgery. Patients are invited to participate if Body Mass Index (BMI) ≥ 35kg/m2 with a comorbidity related to morbid obesity, or a BMI exceeding 40kg/m2.
Intervention: Insertion of the MiniMizer Ring around the gastric pouch in addition to the 'standard' MGB-OAGB.
Main study parameters/endpoints:
Primary Objective:
1. %TBWL 5 years after surgery.
Secondary Objectives: 2. Percentage Excess Weight Loss (%EWL) 5 years after surgery. 3. Decrease or reduction of comorbidities (diabetes mellitus, hypertension, hyperlipidemia, sleep apnoea, and joint complaints). 4. Improvement of quality of life: SF-36 and OBESI-Q questionnaires. 5. Incidence and severity of dumping syndrome. 6. Incidence and severity of reflux symptoms: GERD-HRQoL questionnaire. 7. Incidence and complications due to silicone band.
Measurement of objectives are before surgery and six times after surgery combined with the standard postoperative care for patients who undergo bariatric surgery:
Expected advantages of bOLGB versus OLGB:
1. Increase of weight reduction, and due to that decrease of comorbidities and/or mortality related to overweight. 2. Long term decrease of weight regain. 3. Decrease of incidence of dumping.
Possible disadvantages of bOLGB versus OLGB:
1. Band-related complications such as erosion, infection, stenosis, or pouch dilatation. 2. Functional gastro-intestinal complains such as dysphagia and reflux.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Almelo, Netherlands
Location status: Recruiting
Marc J van Det, MD PhD
CONTACT
Maureen W Tissik, MD
CONTACT
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Insertion of MiniMizer Gastric Ring in addition to the normal MGB-OAGB
No insertion of Minimizer Gastric Ring in addition to the normal MGB-OAGB
Time frame: 5 Years
Percentage total body weight change 5 years after the procedure
Time frame: 5 years
Change in Percentage Excess Weight (%EWL)
Time frame: 5 years
Change in severity of obesity-related co-morbidities: Type 2 Diabetes Mellitus (changes in HbA1c or use of antidiabetic medication), Hypertension (changes in bloodpressure or changes in use of antihypertensives), Osteo-arthritis (changes in VAS-score or use of analgesia drugs) , Hyperlipidemia (changes in HDL/LDL ratio, triglycerides or use of statine drugs), Obstructive Sleep Apnea syndrome (changes in use of CPEP treatment or changes is apneu hypopneu idex), and Gastro-Esophageal Reflux Disease (Changes in outcomes of GERD-HR questionnnaire which scoring scale runs from 0 (asymptomatic) to 50 (complete prohibitive) or changes in use of protonpompinhibitors)
Time frame: 5 years
Evalution of changes in outcome of SF-36 Questionnaire 5 years after surgery. Scoring scale is described between 0 (lowest) and 100 (highest) to evaluate patient's welfare
Time frame: 5 years
Evalution of changes in outcome of OBESI-Q Questionnaire 5 years after surgery. Scoring scale is described between 0 (lowest) and 100 (highest) to evaluate patient's welfare
Time frame: 5 years
The presence and severity of complains related to Dumping Syndrome in participants (yes or no)
Time frame: 5 years
The occurrence of short- and long-term complications of the minimizer ring
Contact information is provided by the study sponsor or research team.
Marc J van Det, MD PhD
CONTACT
Maureen Tissink, MD
CONTACT
Marc van Det
Other
Acronym: RiMini
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07059104
Bariatric Surgery, Body Weight
Gothenburg, Sweden
View Trial DetailsNCT06275061
Bariatric Surgery, Body Weight
Guangzhou, Guangdong, China
View Trial DetailsNCT07374445
Bariatric Surgery, Body Weight
Nanjing, China
View Trial DetailsNCT07175805
Bariatric Surgery, Body Weight
Hartford, Connecticut, United States
View Trial Details