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NCT01308788 · ClinicalTrials.gov registry record

Aqueous Suppressant Versus Aqueous Outflow on Ocular Blood Flow

A clinical trial of Glaucoma, sponsored by Indiana University.

Completed
Registry status
35
Enrollment target
1
Study location

NCT01308788 is a study of Glaucoma that has completed, run by Indiana University. The registered enrollment target is 35 participants, below the 910-participant average among 92 other Glaucoma trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01308788, a study of Glaucoma, has completed, sponsored by Indiana University.

COMPLETED
Registry status
35 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study will be to compare the aqueous production suppressant to aqueous outflow drugs in terms of the response to known vascular parameters. Specifically; systemic perfusion pressure, retrobulbar blood flow and retinal microcirculation.

Conditions Studied

Study Locations (1)

Indiana

  • Department of Ophthalmology Indiana University School of Medicine - Indianapolis

Trial Details

FieldValue
Enrollment Target 35 participants
Start Date 2011-03
Est. Completion 2012-10

Sponsor

Indiana University

890 total trials

What the Registry Record Tells You About NCT01308788

The ClinicalTrials.gov registry entry for NCT01308788 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 35 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 910-participant average among 92 other Glaucoma trials with a reported enrollment target (96% lower). The listed sponsor is Indiana University, which has 890 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Glaucoma appearing as the primary indexed condition, and to 0 interventions.

NCT01308788 reports 1 study location spanning 1 distinct geographic area - top geographies include Indiana.

Frequently Asked Questions

What is clinical trial NCT01308788 about?

NCT01308788 is a clinical study titled "Aqueous Suppressant Versus Aqueous Outflow on Ocular Blood Flow". The purpose of this study will be to compare the aqueous production suppressant to aqueous outflow drugs in terms of the response to known vascular parameters. Specifically; systemic perfusion pressure, retrobulbar blood flow and retinal microcirculation.

What is the current status of trial NCT01308788?

This trial is currently completed. The enrollment target is 35 participants. The study started on 2011-03. Estimated completion is 2012-10.

What conditions does trial NCT01308788 study?

This clinical trial studies the following conditions: Glaucoma.

Who is sponsoring clinical trial NCT01308788?

This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01308788 being conducted?

This trial has 1 study location across Indiana. 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

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.