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NCT00755183 · ClinicalTrials.gov registry record · Phase 2

Safety and Efficacy Study of a Testosterone Eye Drop for the Treatment of Meibomian Gland Dysfunction

A Phase 2 study, sponsored by ORA.

Completed
Registry status
Phase 2
Development phase
60
Enrollment target

NCT00755183 is a Phase 2 study that has completed, run by ORA. The registered enrollment target is 60 participants.

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The verdict

NCT00755183, a Phase 2 study, has completed, sponsored by ORA.

COMPLETED
Registry status
Phase 2
Development phase
60 participants
Enrollment target

Study Summary

The objective of this study is to assess the safety and efficacy of testosterone 0.03% ophthalmic solution compared to vehicle for the treatment of meibomian gland dysfunction.

Interventions

  • DRUG testosterone ophthalmic solution
  • DRUG vehicle of testosterone ophthalmic solution

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2008-07
Est. Completion 2009-04
Phase Phase 2

Sponsor

ORA

19 total trials

What the Registry Record Tells You About NCT00755183

The ClinicalTrials.gov registry entry for NCT00755183 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is ORA, which has 19 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which testosterone ophthalmic solution is the first listed.

NCT00755183 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00755183 about?

NCT00755183 is a clinical study titled "Safety and Efficacy Study of a Testosterone Eye Drop for the Treatment of Meibomian Gland Dysfunction". The objective of this study is to assess the safety and efficacy of testosterone 0.03% ophthalmic solution compared to vehicle for the treatment of meibomian gland dysfunction.

What is the current status of trial NCT00755183?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 60 participants. The study started on 2008-07. Estimated completion is 2009-04.

What interventions are being tested in trial NCT00755183?

The interventions under investigation include: testosterone ophthalmic solution (DRUG), vehicle of testosterone ophthalmic solution (DRUG).

Who is sponsoring clinical trial NCT00755183?

This trial is sponsored by ORA, which has 19 total clinical trials registered on ClinicalTrials.gov.

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

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.