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Azithromycin in the Treatment of M. Avium Complex Lung Disease
This study is ongoing, but not recruiting participants.
First Received: January 11, 2008   No Changes Posted
Sponsor: The University of Texas Health Science Center at Tyler
Collaborator: Pfizer
Information provided by: The University of Texas Health Science Center at Tyler
ClinicalTrials.gov Identifier: NCT00599079
  Purpose

To determine the safety and efficacy of azithromycin in the treatment of lung infection with M.avium complex and M. abscessus lung disease.


Condition Intervention Phase
Mycobacterium Avium Complex
M. Abscessus
Drug: Azithromycin
Phase IV

Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study
Official Title: Open, Noncomparative Trial of Azithromycin in the Treatment of M.Avium Complex (MAC) Lung Disease

Resource links provided by NLM:


Further study details as provided by The University of Texas Health Science Center at Tyler:

Primary Outcome Measures:
  • Clinical and microbiological outcomes such as clinical symptoms and laboratory cultures [ Time Frame: Monthly while on treatment, then followup after therapy discontinuation will be at one month, then at three months, then at six months, then annually and prn for life ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • Microbiological cultures [ Time Frame: Monthly while on treatment, then followup after therapy discontinuation will be at one month, then at three months, then at six months, then annually and prn for life ] [ Designated as safety issue: Yes ]

Enrollment: 66
Study Start Date: February 1993
Estimated Primary Completion Date: August 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1 Drug: Azithromycin
Dosage dependent on clinical factors such as age, weight and patient-specific health status

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Meet American Thoracic Society criteria for nontuberculous lung disease: two or more AFB smear positive, culture positive sputums or bronchoscopic samples and/or two or more AFB smear negative respiratory samples with moderate to heavy growth (2+-4+); abnormal CXR consistent with M. avium lung disease; abnormal CXR consistent with M. avium lung disease; absence of other lung pathogens (except for the coexistence of M. abscessus).
  • Age 18 and older
  • Pretreatment isolate of M. avium complex available for MIC determination

Exclusion Criteria:

  • History of macrolide allergy
  • Received macrolide therapy in last two months
  • Children less than 18 years of age
  • If a menstruating female, not pregnant and on adequate birth control
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00599079

Locations
United States, Texas
The University of Texas Health Science Center at Tyler
Tyler, Texas, United States, 75708
Sponsors and Collaborators
The University of Texas Health Science Center at Tyler
Pfizer
Investigators
Principal Investigator: Richard J Wallace Jr., M.D. The University of Texas Health Science Center at Tyler
  More Information

No publications provided

Responsible Party: The University of Texas Health Science Center at Tyler ( Richard J. Wallace Jr., M.D. )
Study ID Numbers: 340
Study First Received: January 11, 2008
Last Updated: January 11, 2008
ClinicalTrials.gov Identifier: NCT00599079     History of Changes
Health Authority: United States: Food and Drug Administration

Keywords provided by The University of Texas Health Science Center at Tyler:
MAC

Additional relevant MeSH terms:
Bacterial Infections
Anti-Infective Agents
Actinomycetales Infections
Mycobacterium Infections, Atypical
Pharmacologic Actions
Mycobacterium avium-intracellulare Infection
Anti-Bacterial Agents
Gram-Positive Bacterial Infections
Respiratory Tract Diseases
Lung Diseases
Azithromycin
Therapeutic Uses
Mycobacterium Infections

ClinicalTrials.gov processed this record on February 08, 2010