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NCT05289661 · ClinicalTrials.gov registry record · Phase 3

Descemet Endothelial Thickness Comparison Trial I

A Phase 3 study of Fuchs, sponsored by Stanford University.

Active
Registry status
Phase 3
Development phase
160
Enrollment target
7
Study locations

NCT05289661 is a Phase 3 study of Fuchs that is active but no longer recruiting, run by Stanford University. The registered enrollment target is 160 participants. The trial reports 7 study locations across 5 states.

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The verdict

NCT05289661, a Phase 3 study of Fuchs, is active but no longer recruiting, sponsored by Stanford University.

ACTIVE NOT RECRUITING
Registry status
Phase 3
Development phase
160 participants
Enrollment target
7
Study locations

Study Summary

Descemet Endothelial Thickness Comparison Trial (DETECT) I is a multi-center, outcome assessor-masked, placebo-controlled clinical trial randomizing 160 patients in a 2x2 factorial design. The purpose of this study is to determine differences in visual outcomes between two types of corneal transplant surgeries, ultrathin Descemet stripping automated endothelial keratoplasty (UT-DSAEK) and Descemet membrane endothelial keratoplasty (DMEK), and to determine the effect of rho-kinase inhibitors on endothelial cell loss.

Conditions Studied

Interventions

  • DRUG Topical Ripasudil
  • DRUG Topical Placebo

Study Locations (7)

California

  • Stanford University - Palo Alto
  • University of California Davis - Sacramento

Pennsylvania

  • University of Pennsylvania - Philadelphia
  • Wills Eye Hospital - Philadelphia

Florida

  • University of Miami - Palm Beach Gardens

New Hampshire

  • Dartmouth-Hitchcock Medical Center - Lebanon

Oregon

  • Oregon Health & Science University - Portland

Trial Details

FieldValue
Enrollment Target 160 participants
Start Date 2022-07-15
Est. Completion 2027-11-30
Phase Phase 3

Sponsor

Stanford University

1,744 total trials

What the Registry Record Tells You About NCT05289661

The ClinicalTrials.gov registry entry for NCT05289661 describes a study currently listed as active not recruiting, categorized as Phase 3. The registered enrollment target is 160 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Stanford University, which has 1,744 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Fuchs appearing as the primary indexed condition, and to 2 interventions - of which Topical Ripasudil is the first listed.

NCT05289661 reports 7 study locations spanning 5 distinct geographic areas - top geographies include California, Pennsylvania, Florida.

Frequently Asked Questions

What is clinical trial NCT05289661 about?

NCT05289661 is a clinical study titled "Descemet Endothelial Thickness Comparison Trial I". Descemet Endothelial Thickness Comparison Trial (DETECT) I is a multi-center, outcome assessor-masked, placebo-controlled clinical trial randomizing 160 patients in a 2x2 factorial design. The purpose of this study is to determine differences in visual outcomes between two types of corneal transplan...

What is the current status of trial NCT05289661?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 160 participants. The study started on 2022-07-15. Estimated completion is 2027-11-30.

What conditions does trial NCT05289661 study?

This clinical trial studies the following conditions: Fuchs.

What interventions are being tested in trial NCT05289661?

The interventions under investigation include: Topical Ripasudil (DRUG), Topical Placebo (DRUG).

Who is sponsoring clinical trial NCT05289661?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05289661 being conducted?

This trial has 7 study locations across California, Florida, New Hampshire, Oregon, Pennsylvania. 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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