Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 5:13 PM
Ignite Modification Date:
2025-12-24 @ 5:13 PM
NCT ID:
NCT01751750
Eligibility Criteria:
Inclusion Criteria:
\-
Exclusion Criteria:
* Age \<60 years at beginning of study
* Fasting glucose \> 126 mg/dl
* Blood pressure \> 160/100
* Fasting total blood cholesterol \> 280 mg/dl
* Fasting triglycerides \> 300 mg/dl
* Presence of kidney disease, liver disease, gout, hyperthyroidism, untreated or unstable hypothyroidism, certain cancers, gastrointestinal disease, pancreatic disease, other metabolic diseases, or malabsorption syndromes
* Presence of type 2 diabetes requiring the use of oral antidiabetic agents or insulin
* History of bariatric or certain other surgeries related to weight control
* Smokers or other tobacco users (during 6 months prior to the start of the study)
* Consumption of more than 3 servings of tea, wine, or grape juice per day
* Use of supplements containing grape extracts or products
* Use of antibiotics during the intervention or for 3 weeks prior to the intervention period
* History of eating disorders, dietary patterns, or supplement use which will interfere with the goal of the intervention
* Volunteers who have lost 10% of body weight within the last 4 months
* Volunteers who are unable or unwilling to give informed consent or communicate with study staff
* Volunteers who self-report of alcohol or substance abuse within the past 12 months and/or current acute treatment or rehabilitation program for these problems (long-term participation in Alcoholics Anonymous is not an exclusion)
* Other medical, psychiatric, or behavioral factors that in the judgment of the Principal Investigator may interfere with study participation or the ability to follow the intervention protocol
Healthy Volunteers:
True
Sex:
ALL
Maximum Age:
59 Years
Study:
NCT01751750
Study Brief:
Protocol Section:
NCT01751750