Geneva, 1211, Switzerland
NCT Number: NCT02706067
Multifactorial Approach Associated With Orlistat (Xenical) for 4 Years Weight Loss Maintenance in Obese Adults
This study will evaluate the efficacy of a multifactorial approach associated with orlistat (Xenical) in weight loss maintenance during 4 years. The effect of orlistat in combination with diet, physical activity, and/or cognitive behavioral therapy will be monitored.
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Notify MeKey information
Conditions
Age range
18 year–65 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 4
Primary location
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Body mass index (BMI) greater than or equal to (>/=) 30 kilograms per meter-squared (kg/m^2), or BMI >/= 28 kg/m^2 with risk factors of diabetes, hypertension, or hyperlipidemia, before weight loss
- Documented weight loss >/= 10% of initial body weight obtained with diet, with or without psychological therapy or orlistat
Exclusion criteria
- Pregnant or lactating females
- History or presence of significant medical disorders
- Active gastrointestinal disorders such as peptic ulcer disease or malabsorption syndromes
- Pancreatic disease: pancreatic enzyme deficiency, history or current presence of pancreatitis
- Clinically significant abnormal clinical chemistry or hematology results
- Excessive alcohol intake
- Smoking cessation within the previous 6 months
- History or presence of cancer
- Administration of medicines known to alter body weight
- History or presence of cancer
Treatment and study plan
Orlistat
DrugParticipants will receive orlistat on an intermittent basis as 120 milligrams (mg) three times a day: once with breakfast, once with lunch, and once with dinner. In case of weight relapse (increase 2.5 percent [%] or more from Baseline) orlistat will be administered for up to 2 months or until weight regain reaches 0% from Baseline. For special occasions (feasts, birthdays, anniversaries) orlistat will be given for up to 3 days.
Other names: Xenical
Primary outcomes
-
Percent Change from Baseline in Body Weight at Year 2
Time frame: Baseline and Year 2
-
Percent Change from Baseline in Body Weight at Year 4
Time frame: Baseline and Year 4
Secondary outcomes
-
Percentage of Participants Diagnosed with Binge Eating Disorder According to Diagnostic and Statistical Manual of Mental Disorders (DSM) IV Criteria
Time frame: Every 6 months during Year 1, annually during Years 2 to 4
-
Eating Disorder Inventory (EDI) 2 Subscale and Total Score
Time frame: Baseline and Year 4
-
Hospital Anxiety and Depression (HAD) Subscale Score
Time frame: Baseline and Year 4
-
Number of Orlistat Capsules Taken During the Study
Time frame: Given up to three times per day for 4 years
-
Duration of Orlistat Treatment During the Study
Time frame: Given up to three times per day for 4 years
-
Waist-to-Hip Circumference Ratio
Time frame: Baseline and Year 4
-
Waist, Hip, Wrist, and Arm Circumference (Expressed in Centimeters)
Time frame: Baseline and Year 4
-
Skinfold Thickness (Expressed in Millimeters)
Time frame: Baseline and Year 4
-
Bioelectrical Impedance (Expressed in Kilograms of Body Fat Mass)
Time frame: Baseline and Year 4
-
Number of Kilocalories Expended, Total and at Rest
Time frame: Baseline and Year 4
Sponsors and collaborators
Lead sponsor
Hoffmann-La Roche
Industry
Registry information
Official study title
Multifactorial Approach Associated With Orlistat (Xenical) for 4 Years Weight Loss Maintenance in Obese Patients
Important dates
- Study start
- 2002
- Primary completion
- 2009
- Study completion
- 2009
- First posted
- Mar 11, 2016
- Registry last updated
- Apr 5, 2016
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.
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