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CompletedNCT00000907Updated Jul 30, 2008

A Study to Examine the Effects of Stopping Preventive Therapy for Disseminated Mycobacterium Avium Complex (DMAC) in HIV-Positive Patients

An observational study in Mycobacterium Avium-Intracellulare Infection and HIV Infections, sponsored by National Institute of Allergy and Infectious Diseases (NIAID). Completed at 24 sites in United States. Open to participants aged 13 Years and older. Per ClinicalTrials.gov, last updated 2008-07-30.

Sponsored by National Institute of Allergy and Infectious Diseases (NIAID) · Observational

Study type
Observational
Enrollment
50
Ages
13 Years and older
Sex
All
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Study summary

The purpose of this study is to evaluate the effects of stopping preventive therapy for DMAC in HIV-positive patients who (1) have been treated for DMAC for at least 12 months and are now free of any signs of DMAC for at least 16 weeks, and (2) have improved immune systems (CD4 cell counts greater than or equal to 100 cells/mm3) due to anti-HIV drug therapy.

DMAC is a serious and sometimes life-threatening infection that usually affects only HIV-positive patients with CD4 cell counts (cells of the immune system that fight infection) less than 50 cells/mm3. It is recommended that people who are likely to get DMAC be placed on preventive medications which help reduce the risk of infection. New anti-HIV combination drug therapies can increase CD4 cell counts and can reduce the level of HIV in the blood. When CD4 counts are increased, risk of DMAC infection is less. This study examines whether it is possible to stop preventive therapy for DMAC when CD4 counts are high without placing individuals at risk for getting DMAC again.

Read the detailed description

A growing body of evidence suggests AIDS-related morbidity and mortality significantly decrease where potent antiretroviral therapies are used. HAART (highly active antiretroviral therapy) seems to significantly reduce the incidence of MAC. This study tests the validity of those observations.

Peripheral blood cultures and bone marrow (aspirate) samples from 50 eligible patients previously diagnosed with disseminated Mycobacterium avium complex (DMAC) are assessed for microbiologic sterilization of MAC at the time of study entry. If either bone marrow or blood cultures test positive for MAC, patients are discontinued from study. If cultures prove sterile, patients receive 6 weeks of treatment and then discontinue MAC therapy at Week 6 (entry into Step 2 of study). They are then monitored for clinical signs and symptoms of MAC recurrence and for the presence of mycobacteria in blood cultures. In cases of increased viral load during study, modification of antiretroviral therapy is allowed at the discretion of the patient's provider.

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Conditions studied

  • Mycobacterium Avium-Intracellulare Infection
  • HIV Infections

Keywords

  • AIDS-Related Opportunistic Infections
  • Mycobacterium avium-intracellulare Infection
  • Immunity, Cellular
  • Antibiotics, Macrolide
  • Mycobacterium avium Complex
  • CD4 Lymphocyte Count
  • Disease Progression
  • Anti-HIV Agents
03

In context

Mycobacterium avium-intracellulare Infection

73 studies on the registry are indexed under Mycobacterium avium-intracellulare Infection; 8 are open to participants now.

This study's enrollment of 50 is below the median of 100 across 13 observational studies indexed under Mycobacterium avium-intracellulare Infection.

Browse Mycobacterium avium-intracellulare Infection studies →

Lead sponsor

National Institute of Allergy and Infectious Diseases (NIAID) is the lead sponsor of 2,445 studies on the registry; 182 are open to participants now.

Of its 402 completed or terminated interventional studies of FDA-regulated products, 300 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
13 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Patients may be eligible for this study if they:

  • Are HIV-positive.
  • Have 2 CD4 cell counts greater than or equal to 100 cells/mm3 within 60 days and 14 days prior to entry. Measurements must be taken at least 24 hours apart.
  • Have been treated for DMAC with a drug regimen including at least 2 antimycobacterial drugs for at least 12 months, and have been free of symptoms for at least 16 weeks prior to study entry.
  • Have been on anti-HIV therapy for at least 16 weeks and have been on stable anti-HIV therapy for at least 8 weeks prior to study entry.
  • Are at least 13 years old (need consent of parent or guardian if under 18).

Exclusion criteria

Exclusion Criteria

Patients will not be eligible for this study if they:

  • Have any active infection (unless they have been on stable chronic suppressive therapy for at least 3 months).
  • Are pregnant.
05

Study design

Enrollment
50 participants
06

Study locations

24 sites
  • Univ of Southern California / LA County USC Med Ctr
    Los Angeles, California 900331079, United States
  • Willow Clinic
    Menlo Park, California 94025, United States
  • Univ of California / San Diego Treatment Ctr
    San Diego, California 921036325, United States
  • San Francisco AIDS Clinic / San Francisco Gen Hosp
    San Francisco, California 941102859, United States
  • San Francisco Gen Hosp
    San Francisco, California 941102859, United States
  • Santa Clara Valley Med Ctr / AIDS Community Rsch Consortium
    San Jose, California 951282699, United States
  • San Mateo AIDS Program / Stanford Univ
    Stanford, California 943055107, United States
  • Stanford Univ Med Ctr
    Stanford, California 943055107, United States
  • Univ of Colorado Health Sciences Ctr
    Denver, Colorado 80262, United States
  • Univ of Miami School of Medicine
    Miami, Florida 331361013, United States
  • Emory Univ
    Atlanta, Georgia 30308, United States
  • Univ of Hawaii
    Honolulu, Hawaii 96816, United States
  • Rush Presbyterian - Saint Luke's Med Ctr
    Chicago, Illinois 60612, United States
  • Indiana Univ Hosp
    Indianapolis, Indiana 462025250, United States
  • Division of Inf Diseases/ Indiana Univ Hosp
    Indianapolis, Indiana 46202, United States
  • Johns Hopkins Hosp
    Baltimore, Maryland 21287, United States
  • SUNY / Erie County Med Ctr at Buffalo
    Buffalo, New York 14215, United States
  • Beth Israel Med Ctr
    New York, New York 10003, United States
  • Bellevue Hosp / New York Univ Med Ctr
    New York, New York 10016, United States
  • Mount Sinai Med Ctr
    New York, New York 10029, United States
  • Univ of North Carolina
    Chapel Hill, North Carolina 275997215, United States
  • Univ of Cincinnati
    Cincinnati, Ohio 452670405, United States
  • Univ of Pennsylvania at Philadelphia
    Philadelphia, Pennsylvania 19104, United States
  • Julio Arroyo
    West Columbia, South Carolina 29169, United States
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References and documents

Publications

  • Aberg, C. A study of discontinuing maintenance therapy in subjects with disseminated Mycobacterium avium complex. Program and abstracts of the 9th Conference on Retroviruses and Opportunistic Infections. 9th Conference on Retroviruses and Opportunistic Infections. 2002, February 24-28; Seattle Washington (abstract no634)
  • Aberg JA, Williams PL, Liu T, Lederman HM, Hafner R, Torriani FJ, Lennox JL, Dube MP, MacGregor RR, Currier JS; AIDS Clinical Trial Group 393 Study Team. A study of discontinuing maintenance therapy in human immunodeficiency virus-infected subjects with disseminated Mycobacterium avium complex: AIDS Clinical Trial Group 393 Study Team. J Infect Dis. 2003 Apr 1;187(7):1046-52. doi: 10.1086/368413. Epub 2003 Mar 14. PubMed 12660918 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 30, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00000907
First posted
Aug 31, 2001
Last update
Jul 30, 2008

Study contacts

Judith Aberg
study chair
Judith Currier
study chair
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2003. You cannot join it, but the record below documents what was studied.

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