Diet Induced Weight Loss to Reduce Inflammation in Obese Women
NCT ID: NCT01699906
Last Updated: 2014-11-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
22 participants
INTERVENTIONAL
2012-09-30
2014-09-30
Brief Summary
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Detailed Description
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This pilot study of weight loss will be done in 10 very obese post menopausal women. This study will include nutritional and medical evaluation, a 3 day inpatient hospital stay eating a diet providing 50% of what they were taking before starting the study and then a nutritionally adequate diet that will allow them to lose about 10% of their initial weight within 7 to 10 week period. They will have about 4-5 grams of fat removed by suction through a syringe and a biopsy of the skin in addition to studies of blood and stool samples.
When they have completed the study with a 10% body weight loss they will be referred to a nutrition clinic which can counsel them to continue a slower weight loss to an optimal level.
Conditions
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Study Design
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NA
SINGLE_GROUP
BASIC_SCIENCE
NONE
Study Groups
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Dietary intervention
Diet regimen to induce weight loss
Diet regimen to induce weight loss
Diet regimen to induce weight loss
Interventions
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Diet regimen to induce weight loss
Diet regimen to induce weight loss
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Post-menopausal women defined as: 24 consecutive months without a menstrual period, currently not taking any medication known to induce amenorhea
* Body Mass Index 35-50
Exclusion Criteria
* HIV positive
* History of previous weight loss surgery.
* History of Inflammatory Bowel Disease
* History of any other malignancy other than non-melanoma skin cancer in the past 5 years
* Currently taking fish oil, omega-3 supplements or other herbal supplements that exceed GRAS (Generally Recognized as Safe) levels
* Currently taking any estrogen/progesterone hormones except vaginal cream
* Smokers (or stopped \< 3 months ago)
* Currently taking any medication that can alter fat stores as determined by the principal investigator
* Currently taking any weight control medication
* Currently taking hypoglycemic medications.
* Currently taking NSAIDS, aspirin, (if \> once a week, stopped \<30 days ago). Aspirin 81mg may be permitted if the Framingham Risk Score is \< 10
* Currently taking anticoagulant medication or stopped \<30 days ago.
* Screening fasting blood glucose \>165mg/dL
* Screening thyroid function test abnormal
* Screening LFT results \> 2X upper limit of normal
* Screening creatinine \> 2X upper limit of normal
* Any condition or situation which, in the opinion of the investigator, puts the patient at significant risk, could complicate the study results, or may interfere significantly with participation in the study.
40 Years
70 Years
FEMALE
Yes
Sponsors
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Rockefeller University
OTHER
Responsible Party
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Principal Investigators
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Peter R. Holt, MD
Role: PRINCIPAL_INVESTIGATOR
The Rockefeller University
Locations
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The Rockefeller University
New York, New York, United States
Countries
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References
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Aleman JO, Bokulich NA, Swann JR, Walker JM, De Rosa JC, Battaglia T, Costabile A, Pechlivanis A, Liang Y, Breslow JL, Blaser MJ, Holt PR. Fecal microbiota and bile acid interactions with systemic and adipose tissue metabolism in diet-induced weight loss of obese postmenopausal women. J Transl Med. 2018 Sep 3;16(1):244. doi: 10.1186/s12967-018-1619-z.
Other Identifiers
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PHO-0785
Identifier Type: -
Identifier Source: org_study_id
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