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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02043457
Other study ID # HUM00030088
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 2009
Est. completion date December 2025

Study information

Verified date August 2023
Source University of Michigan
Contact Amy E Rothberg, MD, PhD
Phone 734-647-5871
Email arothber@med.umich.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The Investigational Weight Management Clinic now entitled the Weight Management Program at the University of Michigan was created to identify strategies that will result in cost-effective, long term weight management for overweight and obese individuals. The driving hypothesis of the clinic is that the 'one size fits all' philosophy is untenable with a complex disease such as obesity. The clinic will serve as a portal for patients to choose standard clinical care or to explore alternatives from a variety of clinical studies offered through the clinic. These studies will include further investigations into nutrition, the biological basis of weight and weight management and protocols using approved and experimental pharmaceuticals as well as technologies that aid in self-management of weight.


Recruitment information / eligibility

Status Recruiting
Enrollment 3200
Est. completion date December 2025
Est. primary completion date December 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 15 Years to 75 Years
Eligibility Inclusion Criteria: - Obese males and females: age >20 years; Obese population defined as BMI > or = 27 kg/m2 - Lean population BMI < 27 but > 17 kg/m2 - Able and willing to provide written informed consent for the trial Exclusion Criteria: - Evidence of inherited disorders of lipid metabolism. - History of Cancer within the last 5 years - Human immunodeficiency virus (HIV) antibody positive. - Patients with solid organ transplants. - Participation in any other clinical trial within 90 days of entry into this trial. - Pregnant or lactating females. - Uncontrolled thyroid disease - Unstable angina or NY heart association class II failure or above - Gastrointestinal disease specifically GI motility disorders - Unstable neuropsychiatric disease including major depression/anxiety, eating disorder such as binge eating, bulimia or anorexia - End stage renal or hepatic disease - Autoimmune disorders (e.g. SLE) - Body weight fluctuation of more than 5 kg in the previous 3 months - Prior bariatric surgery - A history or current alcohol/substance abuse and change in smoking habits or cessation in the past 6 months. - Women of childbearing age must use a reliable form of contraception. - Any medical condition, which in the opinion of the investigator would make the patient unsuitable for recruitment, or could interfere with the patient participating in or completing the protocol. - Unwilling or unable to consent for the study.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
phenotyping


Locations

Country Name City State
United States University of Michigan Ann Arbor Michigan

Sponsors (1)

Lead Sponsor Collaborator
University of Michigan

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Phenotypic factors related to weight loss and long-term weight maintenance Phenotypic factors include:
blood glucose levels, lipomic/metabolomic measurements, genetic analysis, body fat percentage, maximal oxygen consumption, respiratory quotient, resting metabolic rate, physical/emotional health
Change in phenotypic factors from baseline to 3-6 months and at 2 years
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