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A Phase II Study to Determine the Efficacy and Safety of Sivelestat in Subjects With Acute Lung Injury
NCT00036062 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to determine whether sivelestat will reduce the amount of time a patient must spend on a ventilator and/or increase the chance of survival of patients with acute lung injury.
Conditions Studied
Interventions
- DRUG Sivelestat
Study Locations (20)
Illinois
- — Chicago
- — Elk Grove Village
- — Maywood
- — North Chicago
California
- — Orange
- — Sacramento
- — San Diego
Florida
- — Bay Pines
- — Clearwater
- — Fort Lauderdale
Arizona
- — Phoenix
- — Tucson
Colorado
- — Denver
- — Englewood
Georgia
- — Augusta
- — Austell
Alabama
- — Birmingham
Connecticut
- — New Haven
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 600 participants |
| Start Date | 2001-08 |
| Est. Completion | 2002-12 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00036062
The ClinicalTrials.gov registry entry for NCT00036062 describes a study currently listed as completed. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 600 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Eli Lilly and Company, which has 704 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Acute Lung Injury appearing as the primary indexed condition, and to 1 intervention — of which Sivelestat is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT00036062 reports 20 study locations spanning 10 distinct geographic areas — top geographies include Illinois, California, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT00036062 about?
NCT00036062 is a clinical study titled "A Phase II Study to Determine the Efficacy and Safety of Sivelestat in Subjects With Acute Lung Injury". The purpose of this study is to determine whether sivelestat will reduce the amount of time a patient must spend on a ventilator and/or increase the chance of survival of patients with acute lung injury.
What is the current status of trial NCT00036062?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 600 participants. The study started on 2001-08. Estimated completion is 2002-12.
What conditions does trial NCT00036062 study?
This clinical trial studies the following conditions: Acute Lung Injury, Respiratory Distress Syndrome, Adult. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00036062?
The interventions under investigation include: Sivelestat (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00036062?
This trial is sponsored by Eli Lilly and Company, which has 704 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00036062 being conducted?
This trial has 20 study locations across Alabama, Arizona, California, Colorado, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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