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CompletedNCT00004444Updated Mar 25, 2015

Pilot Randomized Study of Paromomycin (Aminosidine) vs Streptomycin for Uncomplicated Pulmonary Tuberculosis

An interventional study of paromomycin and streptomycin in Tuberculosis, Pulmonary, sponsored by FDA Office of Orphan Products Development. Completed. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2015-03-25.

Sponsored by FDA Office of Orphan Products Development · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
24
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

OBJECTIVES: I. Compare the pharmacokinetics and early bactericidal activity of paromomycin (aminosidine) vs streptomycin for the treatment of uncomplicated pulmonary tuberculosis.

II. Compare the tolerability of these two drugs in these patients. III. Establish the relationships between achieved serum concentration, minimal inhibitory concentration, and early bactericidal activity of paromomycin and streptomycin.

Read the detailed description

PROTOCOL OUTLINE: This is a randomized study. Patients are randomized to one of three treatment arms. Patients in arms I and II receive one of two doses of paromomycin intramuscularly once a day for 3 days. Patients in arm III receive streptomycin intramuscularly once a day for 3 days. All patients then begin a course of standard therapy for tuberculosis.

02

Conditions studied

  • Tuberculosis, Pulmonary

Keywords

  • bacterial infection
  • immunologic disorders and infectious disorders
  • mycobacterium infection
  • mycobacterium tuberculosis infection
  • rare disease
03

In context

Tuberculosis

1,417 studies on the registry are indexed under Tuberculosis; 208 are open to participants now.

This study's enrollment of 24 is below the median of 150 across 952 interventional studies indexed under Tuberculosis.

Browse Tuberculosis studies →

Lead sponsor

FDA Office of Orphan Products Development is the lead sponsor of 31 studies on the registry; none are open to participants now.

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

04

Who can participate

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

Eligibility criteria

PROTOCOL ENTRY CRITERIA:

--Disease Characteristics--

  • Microbiologically proven uncomplicated pulmonary tuberculosis Positive direct sputum smear for acid-fast bacilli OR Presumptive diagnosis based on clinical and radiological findings
  • No known risk factors for multidrug resistant tuberculosis (MDR TB) including: Domicile, shelter, or prison exposure to MDR TB within 6 months Residence in a specific domicile, shelter, or prison cell block within 6 months of a known outbreak of MDR TB Hospitalization, within 6 months, on a medical service or unit in which nosocomial transmission of MDR TB is known to have occurred
  • No clinical evidence of CNS or miliary tuberculosis
  • HIV seronegative

--Prior/Concurrent Therapy--

  • Biologic therapy: At least 12 weeks since immune modulators (including colony-stimulating factors, interferons, or interleukins)
  • Chemotherapy: No concurrent chemotherapy
  • Endocrine therapy: At least 12 weeks since corticosteroids
  • Other: At least 2 years since treatment or prophylaxis for tuberculosis At least 12 weeks since treatment with any drug with activity against tuberculosis, including: All standard drugs used for tuberculosis Clofazimine Rifabutin Quinolones Aminoglycosides At least 12 weeks since pentoxifylline

--Patient Characteristics--

  • Hematopoietic: Absolute neutrophil count at least 1,000/mm3
  • Renal: Creatinine clearance greater than 60 mL/min
  • Pulmonary: No chronic obstructive pulmonary disease
  • Other: Not pregnant Fertile patients must use effective contraception No history of intolerance or known hypersensitivity to aminoglycosides No known or suspected Mycobacterium avium complex infection No other serious, acute infection No diabetes No major organ dysfunction No malignancy requiring chemotherapy
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Enrollment
24 participants

Interventions

  • Drugparomomycin
  • Drugstreptomycin
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Study locations

No study locations are listed for this record.

07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 25, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00004444
Lead sponsor
FDA Office of Orphan Products Development
Collaborators
University of Illinois at Chicago
First posted
Oct 19, 1999
Start date
Nov 1994
Completion
Jan 2001
Last update
Mar 25, 2015

Study contacts

Thomas Paul Kanyok
study chair · University of Illinois at Chicago
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2001. You cannot join it, but the record below documents what was studied.

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