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NCT01060072 · ClinicalTrials.gov registry record · Phase 3

Evaluation of Loteprednol Etabonate Versus Vehicle for the Treatment of Inflammation and Pain Following Cataract Surgery

A Phase 3 study of Pain and Inflammation, sponsored by Bausch & Lomb Incorporated.

Completed
Registry status
Phase 3
Development phase
407
Enrollment target
1
Study location

NCT01060072 is a Phase 3 study of Pain and Inflammation that has completed, run by Bausch & Lomb Incorporated. The registered enrollment target is 407 participants, above the 303-participant average among 374 other Pain trials with a reported enrollment target (34% higher). The trial reports 1 study location across 1 state.

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The verdict

NCT01060072, a Phase 3 study of Pain and Inflammation, has completed, sponsored by Bausch & Lomb Incorporated.

COMPLETED
Registry status
Phase 3
Development phase
407 participants
Enrollment target
1
Study location

Study Summary

This study is being conducted to compare the safety and efficacy of loteprednol etabonate to vehicle for the treatment of postoperative inflammation and pain following cataract surgery.

Conditions Studied

Interventions

  • DRUG Loteprednol etabonate
  • DRUG Vehicle of Loteprednol Etabonate

Study Locations (1)

New York

  • Bausch & Lomb - Rochester

Trial Details

FieldValue
Enrollment Target 407 participants
Start Date 2010-02
Est. Completion 2010-10
Phase Phase 3

Sponsor

Bausch & Lomb Incorporated

174 total trials

What the Registry Record Tells You About NCT01060072

The ClinicalTrials.gov registry entry for NCT01060072 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 407 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 303-participant average among 374 other Pain trials with a reported enrollment target (34% higher). The listed sponsor is Bausch & Lomb Incorporated, which has 174 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Pain appearing as the primary indexed condition, and to 2 interventions - of which Loteprednol etabonate is the first listed.

NCT01060072 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT01060072 about?

NCT01060072 is a clinical study titled "Evaluation of Loteprednol Etabonate Versus Vehicle for the Treatment of Inflammation and Pain Following Cataract Surgery". This study is being conducted to compare the safety and efficacy of loteprednol etabonate to vehicle for the treatment of postoperative inflammation and pain following cataract surgery.

What is the current status of trial NCT01060072?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 407 participants. The study started on 2010-02. Estimated completion is 2010-10.

What conditions does trial NCT01060072 study?

This clinical trial studies the following conditions: Pain, Inflammation.

What interventions are being tested in trial NCT01060072?

The interventions under investigation include: Loteprednol etabonate (DRUG), Vehicle of Loteprednol Etabonate (DRUG).

Who is sponsoring clinical trial NCT01060072?

This trial is sponsored by Bausch & Lomb Incorporated, which has 174 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01060072 being conducted?

This trial has 1 study location across New York. 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

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.