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Search / Trial NCT00505427

Alpha Lipoic Acid and Polycystic Ovary Syndrome

Launched by UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · Jul 20, 2007

Trial Information

Current as of April 30, 2025

Completed

Keywords

Pcos Polycystic Ovary Syndrome Polycystic Ovarian Syndrome Alpha Lipoic Acid Insulin Resistance Oxidative Stress

ClinConnect Summary

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 o...

Gender

FEMALE

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

About University Of California, San Francisco

The University of California, San Francisco (UCSF) is a leading academic institution renowned for its commitment to advancing healthcare through innovative research and clinical trials. With a focus on translating scientific discoveries into effective therapies, UCSF collaborates with a diverse array of stakeholders, including healthcare professionals, industry partners, and patient communities. The university's research programs emphasize interdisciplinary approaches and leverage cutting-edge technology to address complex medical challenges. As a sponsor of clinical trials, UCSF is dedicated to maintaining the highest standards of ethical conduct and scientific rigor, ensuring the safety and well-being of participants while contributing to the broader medical knowledge base.

Locations

San Francisco, California, United States

Patients applied

0 patients applied

Trial Officials

Umesh Masharani, MD

Principal Investigator

University of California, San Francisco

Ira Goldfine, MD

Principal Investigator

University of California, San Francisco

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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