Alpha Lipoic Acid and Polycystic Ovary Syndrome
Primary Purpose
Insulin Resistance, Oxidative Stress
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Alpha Lipoic Acid
Sponsored by
About this trial
This is an interventional treatment trial for Insulin Resistance focused on measuring PCOS, polycystic ovary syndrome, polycystic ovarian syndrome, alpha lipoic acid, insulin resistance, oxidative stress
Eligibility Criteria
Inclusion Criteria:
- PCOS diagnosis
- 18 years of age or older
- Body Mass Index below 35
- Willing to use any form of contraception for the duration of the study
Exclusion Criteria:
- Diabetes
- Pregnancy
- Liver or heart disease or other health problems
- Taking medications that affect insulin resistance
Sites / Locations
- University of California at San Francisco
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT00505427
First Posted
July 20, 2007
Last Updated
June 28, 2013
Sponsor
University of California, San Francisco
Collaborators
National Institutes of Health (NIH)
1. Study Identification
Unique Protocol Identification Number
NCT00505427
Brief Title
Alpha Lipoic Acid and Polycystic Ovary Syndrome
Official Title
Alpha Lipoic Acid and Polycystic Ovary Syndrome
Study Type
Interventional
2. Study Status
Record Verification Date
June 2013
Overall Recruitment Status
Completed
Study Start Date
March 2006 (undefined)
Primary Completion Date
July 2010 (Actual)
Study Completion Date
July 2010 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco
Collaborators
National Institutes of Health (NIH)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The study will recruit 40 subjects with Polycystic Ovary Syndrome (PCOS) as defined by the NIH criteria. The subjects will be pre-screened for insulin sensitivity using fasting insulin and glucose levels and oral glucose tolerance test. The 20 most insulin resistant subjects will undergo measurements of in vivo insulin action by hyperinsulinemic, euglycemic clamp. Body composition will be measured by dual-energy X-ray absorptiometry (DEXA). Plasma lipids and markers of oxidative stress will be measured. They will then receive open label controlled release alpha lipoic acid (CRLA) at 800 mg twice daily for 16 weeks. After treatment hyperinsulinemic euglycemic clamps, DEXA, plasma lipids and markers of oxidative stress will be repeated.
Hypotheses: LA will improve insulin sensitivity in PCOS subjects; LA will reduce oxidative stress, testosterone levels and improve cardiovascular risk factors.
Detailed Description
Insulin resistance commonly occurs in patients with Polycystic Ovary Syndrome (PCOS) and may be responsible for many of the long term complications of PCOS. Patients with PCOS are at increased risk for developing type 2 diabetes and the metabolic syndrome (hypertension, dyslipidemia and cardiovascular disease). Data suggest that oxidative stress contributes to insulin resistance and thus inhibitors of oxidative stress improve insulin action. Alpha Lipoic Acid (LA) is synthesized in the liver and other tissues and is a key component of several mitochondrial enzyme complexes responsible for oxidative glucose metabolism and cellular energy production. When used pharmacologically, LA functions as a safe and effective antioxidant, recycling vitamins C and E,elevating glutathione levels,and lowering reactive oxygen species. Cell culture studies reveal that LA reverses the effects of oxidative stress and improving insulin action. Preliminary clinical data indicate that antioxidants may improve insulin resistance in PCOS patients. We propose, therefore, to study LA's effects on insulin-stimulated glucose uptake (insulin clamp) in a well characterized population of insulin resistant PCOS patients. Because these patients usually present in the adolescent and teenage years, the development of safe, long-term, treatment strategies are needed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insulin Resistance, Oxidative Stress
Keywords
PCOS, polycystic ovary syndrome, polycystic ovarian syndrome, alpha lipoic acid, insulin resistance, oxidative stress
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
22 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Dietary Supplement
Intervention Name(s)
Alpha Lipoic Acid
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
PCOS diagnosis
18 years of age or older
Body Mass Index below 35
Willing to use any form of contraception for the duration of the study
Exclusion Criteria:
Diabetes
Pregnancy
Liver or heart disease or other health problems
Taking medications that affect insulin resistance
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Umesh Masharani, MD
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ira Goldfine, MD
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California at San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
20307398
Citation
Masharani U, Gjerde C, Evans JL, Youngren JF, Goldfine ID. Effects of controlled-release alpha lipoic acid in lean, nondiabetic patients with polycystic ovary syndrome. J Diabetes Sci Technol. 2010 Mar 1;4(2):359-64. doi: 10.1177/193229681000400218.
Results Reference
derived
Learn more about this trial
Alpha Lipoic Acid and Polycystic Ovary Syndrome
We'll reach out to this number within 24 hrs