Pilot Study on the Effect of Oral Controlled-Release Alpha-Lipoic Acid on Oxidative Stress in Adolescents With Type 1 Diabetes Mellitus
Completed · Not applicable
Conditions studied: Diabetes Mellitus, Type 1
In brief
The long-term effects of high blood sugar include blindness, kidney failure, and nerve damage that can ultimately cause loss of limbs. Research has shown that high blood sugar increases the amount of reactive oxygen species (ROS) produced in diabetics, and that the increase in ROS causes damage to eyes, kidneys, and nerves by a process called "oxidative stress." We postulate that alpha-lipoic acid, a potent anti-oxidant, can stop ROS from forming, thereby preventing long-term complications in diabetes. In this pilot study, we will be giving 30 teenagers with type 1 diabetes (T1D) controlled-release alpha-lipoic acid for 3 months, and comparing the amount of oxidative stress before and after treatment. Ten teenagers with T1D will receive placebo instead of alpha-lipoic acid and undergo the same research protocol to aid in validation of outcome measures.
Key facts
- Study ID
- NCT00187564
- Run by
- University of California, San Francisco
- People needed
- 40
- Starts
- 2004-08-01
- Expected to finish
- 2005-10-01
- Last updated by the study team
- 2008-05-06
Who can join
Age: 8 and older, up to 21. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subjects must be pubertal (defined as Tanner stage II or greater), or post-pubertal, with an upper age limit of 21 years.
- Subjects must have diabetes by 1997 ADA criteria:
- fasting plasma glucose >= 126 mg/dL, or
- 2 hour postprandial glucose >= 200 mg/dL
- Subjects must have history of least one auto-antibody associated with T1D, either glutamic acid decarboxylase (GADA) or islet cell autoantigen 512 (ICA512), or history of diabetic ketoacidosis.
You may not qualify if…
- Subjects must not have history of eye, kidney or nerve damage 2. Subjects must not be deemed unable or unlikely to comply with the protocol. Children who are unable to swallow pills, or are unwilling to take pills twice daily will be excluded from the study.
Where it is running
- UCSF Division of Pediatric Endocrinology — San Francisco, California, United States
Full record on ClinicalTrials.gov
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