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NCT00934362 · ClinicalTrials.gov registry record · Phase 2

Effect of Lucinactant on Mucus Clearance in Cystic Fibrosis Lung Disease

A Phase 2 study of Cystic Fibrosis, sponsored by University of North Carolina, Chapel Hill.

Completed
Registry status
Phase 2
Development phase
16
Enrollment target
1
Study location

NCT00934362 is a Phase 2 study of Cystic Fibrosis that has completed, run by University of North Carolina, Chapel Hill. The registered enrollment target is 16 participants, below the 179-participant average among 169 other Cystic Fibrosis trials with a reported enrollment target (91% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00934362, a Phase 2 study of Cystic Fibrosis, has completed, sponsored by University of North Carolina, Chapel Hill.

COMPLETED
Registry status
Phase 2
Development phase
16 participants
Enrollment target
1
Study location

Study Summary

Mucus clearance is impaired in cystic fibrosis. Inhaled surfactants may reduce adhesive forces between mucus and airway surfaces and improve mucus clearance. This in turn my improve lung health. The investigators propose to measure mucus clearance before and after lucinactant or vehicle administration in patients with cystic fibrosis.

Conditions Studied

Interventions

  • DRUG Lucinactant first
  • DRUG Placebo first

Study Locations (1)

North Carolina

  • University of North Carolina - Chapel Hill

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2008-10
Est. Completion 2010-08
Phase Phase 2

What the Registry Record Tells You About NCT00934362

The ClinicalTrials.gov registry entry for NCT00934362 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 16 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 179-participant average among 169 other Cystic Fibrosis trials with a reported enrollment target (91% lower). The listed sponsor is University of North Carolina, Chapel Hill, which has 1,109 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Cystic Fibrosis appearing as the primary indexed condition, and to 2 interventions - of which Lucinactant first is the first listed.

NCT00934362 reports 1 study location spanning 1 distinct geographic area - top geographies include North Carolina.

Frequently Asked Questions

What is clinical trial NCT00934362 about?

NCT00934362 is a clinical study titled "Effect of Lucinactant on Mucus Clearance in Cystic Fibrosis Lung Disease". Mucus clearance is impaired in cystic fibrosis. Inhaled surfactants may reduce adhesive forces between mucus and airway surfaces and improve mucus clearance. This in turn my improve lung health. The investigators propose to measure mucus clearance before and after lucinactant or vehicle administrati...

What is the current status of trial NCT00934362?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 16 participants. The study started on 2008-10. Estimated completion is 2010-08.

What conditions does trial NCT00934362 study?

This clinical trial studies the following conditions: Cystic Fibrosis.

What interventions are being tested in trial NCT00934362?

The interventions under investigation include: Lucinactant first (DRUG), Placebo first (DRUG).

Who is sponsoring clinical trial NCT00934362?

This trial is sponsored by University of North Carolina, Chapel Hill, which has 1,109 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00934362 being conducted?

This trial has 1 study location across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

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