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NCT00002253 · ClinicalTrials.gov registry record · NA
A Multicenter Placebo-Controlled Double Blind Study to Evaluate the Efficacy and Safety of Sandostatin ( SMS 201-995 ) in Patients With Acquired Immunodeficiency Related Diarrhea Who Were Either "Responders" or "Non-Responders" in a Prior Placebo-Controlled Double-Blind Sandostatin Study.
A NA study, sponsored by Sandoz.
- Completed
- Registry status
- NA
- Development phase
NCT00002253 is a NA study that has completed, run by Sandoz.
The verdict
NCT00002253, a NA study, has completed, sponsored by Sandoz.
- COMPLETED
- Registry status
- NA
- Development phase
Study Summary
The primary objective of this study is to determine the relapse rate in patients with AIDS-related diarrhea who were found to be "Responders" in a previous placebo-controlled, double-blind study of Sandostatin (Study #D203 - FDA 102A). The secondary objectives include: 1) To evaluate clinical efficacy and safety of open-label Sandostatin in patients who were "Non-Responders" in Study #D203 - FDA 102A; 2) To evaluate the efficacy and safety of Sandostatin during prolonged open-label treatment in "Responders" from Study #D03 - FDA 102A.
Interventions
- DRUG Octreotide
Trial Details
| Field | Value |
|---|---|
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00002253
The ClinicalTrials.gov registry entry for NCT00002253 describes a study currently listed as completed, categorized as NA. An enrollment target was not published in the registry record, which is common for early-stage or observational entries. The listed sponsor is Sandoz, which has 29 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Octreotide is the first listed.
NCT00002253 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00002253 about?
NCT00002253 is a clinical study titled "A Multicenter Placebo-Controlled Double Blind Study to Evaluate the Efficacy and Safety of Sandostatin ( SMS 201-995 ) in Patients With Acquired Immunodeficiency Related Diarrhea Who Were Either "Responders" or "Non-Responders" in a Prior Placebo-Controlled Double-Blind Sandostatin Study.". The primary objective of this study is to determine the relapse rate in patients with AIDS-related diarrhea who were found to be "Responders" in a previous placebo-controlled, double-blind study of Sandostatin (Study #D203 - FDA 102A). The secondary objectives include: 1) To evaluate clinical effic...
What is the current status of trial NCT00002253?
This trial is currently completed. It is a NA study.
What interventions are being tested in trial NCT00002253?
The interventions under investigation include: Octreotide (DRUG).
Who is sponsoring clinical trial NCT00002253?
This trial is sponsored by Sandoz, which has 29 total clinical trials registered on ClinicalTrials.gov.
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