Viewing Study NCT00002114



Ignite Creation Date: 2024-05-05 @ 9:42 AM
Last Modification Date: 2024-10-26 @ 9:02 AM
Study NCT ID: NCT00002114
Status: COMPLETED
Last Update Posted: 2005-06-24
First Post: 1999-11-02

Brief Title: A Double-Blind Randomized Parallel Group Study Comparing Procysteine to Placebo in HIV-Infected Patients Who Are Taking Antiretroviral Nucleosides
Sponsor: Free Radical Sciences
Organization: NIH AIDS Clinical Trials Information Service

Study Overview

Official Title: A Double-Blind Randomized Parallel Group Study Comparing Procysteine to Placebo in HIV-Infected Patients Who Are Taking Antiretroviral Nucleosides
Status: COMPLETED
Status Verified Date: 1994-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: To compare the efficacy and safety of orally administered Procysteine with placebo in HIV-infected patients who are receiving 1 of the following 1 zidovudine AZT alone 2 didanosine ddI alone 3 AZT plus ddI or 4 AZT plus zalcitabine ddC
Detailed Description: All patients must receive treatment with antiretroviral nucleosides in addition to study treatment Patients are randomized equally into 1 of 3 outpatient dosage groups Group 1 receives placebo Group 2 receives a low dose of Procysteine and Group 3 receives a higher dose of Procysteine Patients receive study treatment for 6 months total duration of patient participation is 30 weeks

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?:
Secondary IDs
Secondary ID Type Domain Link
CN9202D None None None