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Bacterial Infections clinical trials

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NCT ID: NCT00004829 Completed - Cystic Fibrosis Clinical Trials

Phase III Randomized Study of the Inhalation of Tobramycin in Patients With Cystic Fibrosis

Start date: June 1995
Phase: Phase 3
Study type: Interventional

OBJECTIVES: I. Determine the safety and efficacy of tobramycin in patients with cystic fibrosis who are chronically colonized with Pseudomonas aeruginosa. II. Determine whether this treatment produces tobramycin-resistant bacteria at a frequency different from the placebo group and whether the emergence of resistance is associated with a lack of clinical response.

NCT ID: NCT00004747 Completed - Cystic Fibrosis Clinical Trials

Phase II Randomized, Double-Blind, Placebo-Controlled Study of Intravenous Mucoid Exopolysaccharide Pseudomonas Aeruginosa Immune Globulin for Cystic Fibrosis

Start date: July 1995
Phase: Phase 2
Study type: Interventional

OBJECTIVES: I. Assess the efficacy of monthly intravenous mucoid exopolysaccharide Pseudomonas aeruginosa immune globulin (MEP IGIV) given over 1 year in reducing the frequency of acute pulmonary exacerbation in patients with cystic fibrosis, mild to moderate pulmonary disease, and mucoid P. aeruginosa colonization. II. Assess the effect of MEP IGIV on FEV1, sputum density of mucoid P. aeruginosa, and the quality of life in these patients. III. Assess the safety of monthly MEP IGIV. IV. Assess population-based MEP IGIV pharmacokinetics during chronic therapy.

NCT ID: NCT00002344 Completed - HIV Infections Clinical Trials

A Study of Azithromycin in HIV-Infected Patients

Start date: n/a
Phase: Phase 1
Study type: Interventional

To assess the dose proportionality of azithromycin concentrations and toleration when delivered in tablet formulation to HIV-infected patients. The need exists to further assess the antibacterial agent azithromycin at differing doses in an HIV-infected population.

NCT ID: NCT00002139 Completed - HIV Infections Clinical Trials

Phase I Study of the Clinical Pharmacology of Azithromycin in Buffy Coat of HIV-Infected Subjects.

Start date: n/a
Phase: Phase 1
Study type: Interventional

To compare the uptake of azithromycin in white cells relative to plasma concentrations in HIV-infected patients.

NCT ID: NCT00000826 Completed - HIV Infections Clinical Trials

Effect of Fluconazole, Clarithromycin, and Rifabutin on the Pharmacokinetics of Sulfamethoxazole-Trimethoprim and Dapsone and Their Hydroxylamine Metabolites

Start date: n/a
Phase: Phase 1
Study type: Interventional

To determine the effects of fluconazole and either rifabutin or clarithromycin, alone and in combination, on the pharmacokinetics of first sulfamethoxazole-trimethoprim and then dapsone in HIV-infected patients. Although prophylaxis for more than one opportunistic infection is emerging as a common clinical practice in patients with advanced HIV disease, little is known about possible adverse drug interactions. The need exists to define pharmacokinetics and pharmacodynamic adverse interactions of the many combination prophylactic regimens that may be prescribed.

NCT ID: NCT00000811 Completed - HIV Infections Clinical Trials

A Study to Compare Different Drugs Used to Prevent Serious Bacterial Infections in HIV-Positive Children

Start date: n/a
Phase: Phase 2
Study type: Interventional

This study compares 2 different treatments administered to try to prevent serious bacterial infections (such as pneumonia) in HIV-positive children. A combination of drugs (azithromycin plus atovaquone) will be compared to sulfamethoxazole-trimethoprim (SMX/TMP) alone. This study also evaluates the long-term safety and tolerance of these different drugs. SMX/TMP is a commonly prescribed drug for the prevention of bacterial infections. However, the combination of azithromycin and atovaquone may be safer and more effective than SMX/TMP. This study compares the 2 treatments.