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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02348762
Other study ID # H-34686 Glutathione and Aging
Secondary ID
Status Completed
Phase Phase 1
First received
Last updated
Start date November 2014
Est. completion date March 2021

Study information

Verified date January 2022
Source Baylor College of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators have previously reported that older patients with HIV are deficient in glutathione (GSH) due to decreased availability of cysteine and glycine, and that oral supplementation with cysteine (as n-acetylcysteine) and glycine for 2-weeks corrects their own levels, and improves concentrations of red-cell GSH. The investigators also found that when GSH deficient, subjects had impaired mitochondrial energetics and this improved with an increase in intracellular GSH concentrations. The current proposal will investigate if cysteine and glycine supplementation for a duration of 24 weeks will result in changes in : (a) GSH levels; (b) body composition/anthropometry; (c) strength and function; (d) quality of life; (e) mitochondrial energetics; (f) biochemistry (including dyslipidemia and oxidative stress); (g) protein and glucose metabolism; (h) cognition and memory. 3 months after completing supplementation, measurement of GSH concentrations, strength, function, mitochondrial energetics and neurocognitive tests will be done to determine the effects of washout.


Description:

Data not available at present


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date March 2021
Est. primary completion date November 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 80 Years
Eligibility Inclusion Criteria: Older subjects: - age 70-80 years; Younger subjects: - age 21-30 years Exclusion Criteria: 1. No known diabetes, liver disease, kidney disease, coronary heart disease, stroke, or cancer; 2. Any limitations in ability to walk; 3. Triglyceride concentrations greater than 500 mg/dl (if lipid lowering medications are stopped); 4. BMI less than 20.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Cysteine (as n-acetylcysteine) and Glycine
Older subjects will be studied before and after receiving cysteine and glycine

Locations

Country Name City State
United States Baylor Metabolic Research Unit (MRU) Houston Texas

Sponsors (1)

Lead Sponsor Collaborator
Baylor College of Medicine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Red blood cell concentrations of Glutathione measured by HPLC 8 months
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