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NCT00716742 · ClinicalTrials.gov registry record

Safety and Efficacy Study of Bimatoprost, Latanoprost, and Travoprost in Patients With Elevated Intraocular Pressure (IOP) and Open-angle Glaucoma (OAG)

A clinical trial, sponsored by Allergan.

Completed
Registry status
1,099
Enrollment target

NCT00716742: Completed study, sponsored by Allergan.

NCT00716742 is a clinical trial that has completed, run by Allergan. The registered enrollment target is 1,099 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00716742 has completed, sponsored by Allergan.

COMPLETED
Registry status
1,099 participants
Enrollment target

Study Summary

To investigate the effectiveness of the newer IOP-lowering therapies, as prescribed in normal clinical practice, in larger patient numbers. Patients will be assessed at baseline, at each follow-up visit (follow-up visits are variable as per physician discretion) and at final follow-up visit.

Primary Outcome

Change from baseline in bilateral (both eyes) IOP at the 1 year follow-up visit. IOP is a measure of the fluid pressure inside the eye. The bilateral IOP was calculated as an average between both eye's IOP. A negative number change from baseline indicates reduction in IOP (improvement).

Interventions

  • DRUG bimatoprost 0.03%, latanoprost 0.005%, and travoprost 0.004%

Trial Details

FieldValue
Enrollment Target 1,099 participants
Start Date 2004-09
Est. Completion 2009-09
Allergan

314 total trials

What the finished NCT00716742 record still lists

NCT00716742 is an observational study that tracks outcomes without assigning an intervention. Its 1,099 participants enrollment target places it among the larger protocols in the corpus.

The record links to 0 conditions, and to 1 intervention - of which bimatoprost 0.03%, latanoprost 0.005%, and travoprost 0.004% is the first listed.

NCT00716742 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00716742 about?

NCT00716742 is a clinical study titled "Safety and Efficacy Study of Bimatoprost, Latanoprost, and Travoprost in Patients With Elevated Intraocular Pressure (IOP) and Open-angle Glaucoma (OAG)". To investigate the effectiveness of the newer IOP-lowering therapies, as prescribed in normal clinical practice, in larger patient numbers. Patients will be assessed at baseline, at each follow-up visit (follow-up visits are variable as per physician discretion) and at final follow-up visit.

What is the current status of trial NCT00716742?

This trial is currently completed. The enrollment target is 1,099 participants. The study started on 2004-09. Estimated completion is 2009-09.

What interventions are being tested in trial NCT00716742?

The interventions under investigation include: bimatoprost 0.03%, latanoprost 0.005%, and travoprost 0.004% (DRUG).

Who is sponsoring clinical trial NCT00716742?

This trial is sponsored by Allergan, which has 314 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT00716742, the US trial registry maintained by the National Library of Medicine. NCT00716742 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.