Durham VA Medical Center HSR&D COE
Durham, North Carolina, 27705, United States
NCT Number: NCT00108524
This study compares two types of diet interventions: a low carbohydrate ketogenic diet (Atkins) and a low-fat diet combined with a medication (Orlistat).
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Notify Me18 year–69 year
All sexes
Interventional
Not applicable
Durham, North Carolina, 27705, United States
Overweight and obesity are increasingly prevalent in the veteran population as well as the general public. For patients with obesity-associated illnesses, there are few effective treatment options available after failed attempts at diet and exercise, even though weight loss has been shown to alleviate these conditions. The purpose of this study is to compare the tolerability, safety, and efficacy of a low-carbohydrate ketogenic diet (Atkins) with a combination of a low-fat diet and Orlistat. The outcomes examined over a 48 week duration will include body weight, risk factors for heart disease (e.g., lipid profiles), and blood sugar. This is a randomized, parallel-intervention trial. Subjects (n=150) will be recruited from the Durham VAMC Ambulatory Care Clinics. All patients receive one of the two intensive weight loss interventions.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
A low-carb diet limits carbohydrates - such as grains, starchy vegetables and fruit - and emphasizes dietary protein and fat.
In addition to the low fat diet, Orlistat is taken 3 times daily.
Other names: Xenical
Participants receive counseling on a low fat diet over 48 weeks aimed at reducing fat and calorie intake
Time frame: baseline and 48 weeks
Body weight was measured using the same calibrated scale (Tanita Corp, Arlington Heights, Illinois) at each visit at the same time of day, with the participant wearing light clothing and no shoes.
Time frame: baseline and 48 weeks
Measured change in low-density lipoprotein cholesterol, or LDL-C, from baseline to 48 weeks.
Time frame: Baseline and 48 weeks
Measured change in Fasting glucose, mg/dL, from baseline to 48 weeks.
US Department of Veterans Affairs
Fed
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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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