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NCT00606242 · ClinicalTrials.gov registry record · Phase 4
Dose Response Effects of Inhaled Fluticasone on Airway Effects of Hypertonic-saline in Asthma
A Phase 4 study of Asthma, sponsored by University of California, San Francisco.
- Completed
- Registry status
- Phase 4
- Development phase
- 44
- Enrollment target
- 1
- Study location
NCT00606242 is a Phase 4 study of Asthma that has completed, run by University of California, San Francisco. The registered enrollment target is 44 participants, below the 1,563-participant average among 374 other Asthma trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00606242, a Phase 4 study of Asthma, has completed, sponsored by University of California, San Francisco.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 44 participants
- Enrollment target
- 1
- Study location
Study Summary
This study investigates the effect of a inhaled corticosteroid (fluticasone or "Flovent") on airway narrowing induced by hypertonic saline (salty water). The study hypothesis is that fluticasone will be more effective in preventing saline-induced airway narrowing than methacholine-induced narrowing.
Conditions Studied
Interventions
- DRUG Fluticasone
Study Locations (1)
California
- University of California, San Francisco - San Francisco
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 44 participants |
| Start Date | 2000-01 |
| Est. Completion | 2007-12 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00606242
The ClinicalTrials.gov registry entry for NCT00606242 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 44 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,563-participant average among 374 other Asthma trials with a reported enrollment target (97% lower). The listed sponsor is University of California, San Francisco, which has 1,713 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Asthma appearing as the primary indexed condition, and to 1 intervention - of which Fluticasone is the first listed.
NCT00606242 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT00606242 about?
NCT00606242 is a clinical study titled "Dose Response Effects of Inhaled Fluticasone on Airway Effects of Hypertonic-saline in Asthma". This study investigates the effect of a inhaled corticosteroid (fluticasone or "Flovent") on airway narrowing induced by hypertonic saline (salty water). The study hypothesis is that fluticasone will be more effective in preventing saline-induced airway narrowing than methacholine-induced narrowing.
What is the current status of trial NCT00606242?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 44 participants. The study started on 2000-01. Estimated completion is 2007-12.
What conditions does trial NCT00606242 study?
This clinical trial studies the following conditions: Asthma.
What interventions are being tested in trial NCT00606242?
The interventions under investigation include: Fluticasone (DRUG).
Who is sponsoring clinical trial NCT00606242?
This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00606242 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.