ClinicalTrials.gov
 Home    Search    Study Topics    Glossary  
 

  Full Text View  
  Tabular View  
  Contacts and Locations  
  No Study Results Posted  
  Related Studies  
Use of a Test That Evaluates How the Body Handles Insulin and Glucose

This study has been completed.

Sponsored by: National Institute of Allergy and Infectious Diseases (NIAID)
Information provided by: National Institute of Allergy and Infectious Diseases (NIAID)
ClinicalTrials.gov Identifier: NCT00027092
  Purpose

The purpose of this study is to find out if testosterone gel affects how the body handles insulin and glucose.

Specific anti-HIV treatments may increase a patient's risk of certain diseases by causing metabolic problems such as reduced sensitivity to insulin. This substudy will examine how testosterone affects insulin sensitivity. If testosterone increases insulin sensitivity in the patients, then giving testosterone to HIV-infected patients may allow the continuation of anti-HIV treatments without increasing the patients' risk of disease. The test used to determine insulin sensitivity will be a modified frequently sampled intravenous glucose tolerance test (FSIVGTT), which can accurately measure insulin sensitivity.


Condition
HIV Infections

MedlinePlus related topics:   AIDS   

Drug Information available for:   Testosterone    Methyltestosterone    Oxymesterone    Testosterone enanthate    Testosterone Propionate    Testosterone undecanoate    Insulin    Dextrose   

U.S. FDA Resources

Study Type:   Observational
Official Title:   AACTG Modified Frequently Sampled Intravenous Glucose Tolerance Test (FSIVGTT) for the Assessment of Insulin Sensitivity: A Substudy of A5079

Further study details as provided by National Institute of Allergy and Infectious Diseases (NIAID):

Estimated Enrollment:   50

Detailed Description:

Assessment of insulin sensitivity is an important objective of this substudy. Extrapolation from earlier studies suggests that insulin resistance will be associated with low testosterone levels at baseline in HIV-infected men with visceral obesity and that physiologic testosterone replacement in these individuals is likely to increase insulin sensitivity. However, direct assessment of insulin sensitivity under carefully controlled conditions is crucial to understanding the full metabolic impact of physiologic testosterone replacement in the context of A5079. The FSIVGTT, using the Bergman minimal model, has become a widely used method for the assessment of insulin sensitivity in epidemiological and intervention studies. Based on these considerations, the modified FSIVGTT was chosen as the optimal modality to assess insulin sensitivity in A5112s.

This study is a substudy of A5079. Patients enrolled in A5079 are eligible for this substudy but receive no study treatment other than that which they receive on A5079. Insulin sensitivity is measured by FSIVGTT performed at entry and at Weeks 24 and 48. In the modified FSIVGTT, 15 serial blood specimens for glucose are drawn over a 245-minute interval. The FSIVGTT assesses whether patients given testosterone supplements have more sensitivity to insulin than patients given a placebo.

  Eligibility
Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria

Patients may be eligible for this study if they:

  • Are enrolled in A5079.
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00027092

Locations
United States, California
Univ of Southern California / LA County USC Med Ctr    
      Los Angeles, California, United States, 900331079
Univ of California San Francisco    
      San Francisco, California, United States, 94110
United States, Hawaii
Univ of Hawaii    
      Honolulu, Hawaii, United States, 96816
United States, Illinois
Rush Presbyterian - Saint Luke's Med Ctr    
      Chicago, Illinois, United States, 60612
United States, Indiana
Indiana Univ Hosp    
      Indianapolis, Indiana, United States, 462025250
Methodist Hosp of Indiana / Life Care Clinic    
      Indianapolis, Indiana, United States, 46202
Wishard Hosp    
      Indianapolis, Indiana, United States, 46202
United States, New York
Bellevue Hosp / New York Univ Med Ctr    
      New York, New York, United States, 10016

Sponsors and Collaborators

Investigators
Study Chair:     Shalender Bhasin    
  More Information


Haga clic aquí para ver información sobre este ensayo clínico en español.  This link exits the ClinicalTrials.gov site
 

Study ID Numbers:   ACTG A5112s, AACTG A5112s
First Received:   November 20, 2001
Last Updated:   August 6, 2008
ClinicalTrials.gov Identifier:   NCT00027092
Health Authority:   United States: Federal Government

Keywords provided by National Institute of Allergy and Infectious Diseases (NIAID):
Infusions, Intravenous  
Testosterone  
Insulin Resistance  
Hormone Replacement Therapy  
Glucose Tolerance Test  

Study placed in the following topic categories:
Virus Diseases
Testosterone
Sexually Transmitted Diseases, Viral
HIV Infections
Sexually Transmitted Diseases
Acquired Immunodeficiency Syndrome
Methyltestosterone
Insulin Resistance
Retroviridae Infections
Insulin
Immunologic Deficiency Syndromes
Testosterone 17 beta-cypionate

Additional relevant MeSH terms:
RNA Virus Infections
Slow Virus Diseases
Immune System Diseases
Lentivirus Infections
Infection

ClinicalTrials.gov processed this record on December 03, 2008




Links to all studies - primarily for crawlers