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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00599079
Other study ID # 340
Secondary ID
Status Completed
Phase Phase 4
First received January 11, 2008
Last updated May 19, 2017
Start date February 1993
Est. completion date May 18, 2017

Study information

Verified date May 2017
Source The University of Texas Health Science Center at Tyler
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


Description:

To study the safety and efficacy of azithromycin in combination treatment for M. abscessus and MAC lung disease


Recruitment information / eligibility

Status Completed
Enrollment 66
Est. completion date May 18, 2017
Est. primary completion date May 2008
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Azithromycin
Azithromycin Daily Dosage dependent on clinical factos such as age, weight and patient specific health descriptors

Locations

Country Name City State
United States The University of Texas Health Science Center at Tyler Tyler Texas

Sponsors (2)

Lead Sponsor Collaborator
The University of Texas Health Science Center at Tyler Pfizer

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical and microbiological outcomes such as clinical symptoms and laboratory cultures neg cultures X3( sputum conversion) 6 months
Secondary Microbiological cultures culture neg 1 yr on treatment 1yr
See also
  Status Clinical Trial Phase
Completed NCT00598897 - Use of Clarithromycin and Rifabutin for the Treatment of M. Avium Complex (MAC) Lung Disease Phase 4