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NCT01114893 · ClinicalTrials.gov registry record · Phase 2

Travoprost Five Day Posology Study

A Phase 2 study of Ocular Hypertension and Open Angle Glaucoma (OAG), sponsored by Alcon Research.

Completed
Registry status
Phase 2
Development phase
60
Enrollment target
1
Study location

NCT01114893 is a Phase 2 study of Ocular Hypertension and Open Angle Glaucoma (OAG) that has completed, run by Alcon Research. The registered enrollment target is 60 participants, below the 277-participant average among 54 other Ocular Hypertension trials with a reported enrollment target (78% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01114893, a Phase 2 study of Ocular Hypertension and Open Angle Glaucoma (OAG), has completed, sponsored by Alcon Research.

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

Study Summary

The purpose of this study is to determine the safety and efficacy of three concentrations of travoprost ophthalmic solution (Groups A, B and C) administered eight times daily.

Interventions

  • DRUG Travoprost 0.004%
  • DRUG Travoprost Vehicle
  • DRUG Travoprost (Groups A, B and C)

Study Locations (1)

Texas

  • Contact Alcon Call Center For Trial Locations - Fort Worth

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2010-04
Phase Phase 2

Sponsor

Alcon Research

275 total trials

What the Registry Record Tells You About NCT01114893

The ClinicalTrials.gov registry entry for NCT01114893 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, below the 277-participant average among 54 other Ocular Hypertension trials with a reported enrollment target (78% lower). The listed sponsor is Alcon Research, which has 275 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Ocular Hypertension appearing as the primary indexed condition, and to 3 interventions - of which Travoprost 0.004% is the first listed.

NCT01114893 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT01114893 about?

NCT01114893 is a clinical study titled "Travoprost Five Day Posology Study". The purpose of this study is to determine the safety and efficacy of three concentrations of travoprost ophthalmic solution (Groups A, B and C) administered eight times daily.

What is the current status of trial NCT01114893?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 60 participants. The study started on 2010-04.

What conditions does trial NCT01114893 study?

This clinical trial studies the following conditions: Ocular Hypertension, Open Angle Glaucoma (OAG).

What interventions are being tested in trial NCT01114893?

The interventions under investigation include: Travoprost 0.004% (DRUG), Travoprost Vehicle (DRUG), Travoprost (Groups A, B and C) (DRUG).

Who is sponsoring clinical trial NCT01114893?

This trial is sponsored by Alcon Research, which has 275 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01114893 being conducted?

This trial has 1 study location across Texas. 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 Editorial

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