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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00598897
Other study ID # 447
Secondary ID
Status Completed
Phase Phase 4
First received January 11, 2008
Last updated May 19, 2017
Start date August 1995
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 tolerance of clarithromycin given three times per week in combination with multiple drugs including rifabutin three times per week


Description:

Safety and tolerance of clarithromycin given 3 times weekly with multiple drugs including ethambutol and rifampin/rifabutin


Recruitment information / eligibility

Status Completed
Enrollment 89
Est. completion date May 18, 2017
Est. primary completion date August 7, 2002
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Meet American Thoracic Society criteria for nontuberculous mycobacterial 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; absence of other potential mycobacterial or fungal lung pathogens (except for the coexistence of M. abscessus).

- Adults age 18 and older

- Pretreatment isolate of M. avium complex available for MIC determination

Exclusion Criteria:

- History of allergy to study drugs

- If a mensruating female, not pregnant and on adequate birth control.

- Children less than 18 years of age

- HIV + or at high risk for HIV infection.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
clarithromycin, rifabutin
Clarithromycin three times per week (variable dosage) in combination with multiple drugs including rifabutin or rifampin three times per week (variable dosage). Dosage dependent on age, weight and other patient-specific health factors.

Locations

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

Sponsors (3)

Lead Sponsor Collaborator
The University of Texas Health Science Center at Tyler Abbott, 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 sputum conversion culture neg x3 6 months
Secondary Clinical and microbiological outcomes culture neg 1 yr on treatment 1 yr
See also
  Status Clinical Trial Phase
Completed NCT00599079 - Azithromycin in the Treatment of M. Avium Complex Lung Disease Phase 4