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Clinical Research Directory

Browse clinical research sites, groups, and studies.

4 clinical studies listed.

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Fuchs

Tundra lists 4 Fuchs clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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ACTIVE NOT RECRUITING

NCT05289661

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 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.

Gender: All

Ages: 18 Years - Any

Updated: 2026-08-17

5 states

Fuchs
RECRUITING

NCT05275972

Descemet Endothelial Thickness Comparison Trial II

Descemet Endothelial Thickness Comparison Trial (DETECT) II is a multi-center, outcome assessor-masked, placebo-controlled clinical trial randomizing 60 patients with Fuchs endothelial dystrophy to DMEK versus Descemet Stripping Only (DSO) with adjunctive Ripasudil.

Gender: All

Ages: 18 Years - Any

Updated: 2026-08-17

5 states

Fuchs
Fuchs Dystrophy
Fuchs' Endothelial Dystrophy
NOT YET RECRUITING

NCT07729137

Study of EO2002 in Subjects With Corneal Edema Secondary to Corneal Endothelial Dysfunction

This study will evaluate the safety and effectiveness of a single injection of EO2002 at one of two dose levels (150,000 or 500,000 magnetic human corneal endothelial cells \[mHCECs\]), compared with a placebo injection, in participants with corneal edema caused by corneal endothelial dysfunction.

Gender: All

Ages: 21 Years - Any

Updated: 2026-07-29

1 state

Corneal Edema
Fuchs
Fuchs Dystrophy
+9
RECRUITING

NCT07024693

DT-168 in Keratoplasty Patients With Fuchs Endothelial Corneal Dystrophy

The purpose of this study is to evaluate the pharmacodynamics, safety, and tolerability of DT-168 Ophthalmic Solution in pre-keratoplasty patients with Fuchs endothelial corneal dystrophy.

Gender: All

Ages: 30 Years - Any

Updated: 2025-12-29

2 states

Fuchs Endothelial Corneal Dystrophy
Fuchs