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RECRUITING Phase 2

ExCrossV Multi Site Trial for Vascularized High Risk Keratoplasty

NCT06753916 · View on ClinicalTrials.gov ↗

Study Summary

The main objective of this study is to determine the safety of Ex Vivo Cross Linking (CXL) of donor corneal tissue in participants who have undergone high-risk penetrating keratoplasty.

Conditions Studied

Interventions

  • PROCEDURE Corneal Donor Tissue with Cross Linking
  • PROCEDURE Corneal Donor Tissue without Cross Linking

Study Locations (12)

California

  • University of California Irvine - Gavin Herbert Eye Institute — Irvine
  • The University of California Los Angeles - Doris Stein Eye Research Center — Los Angeles
  • University of California San Francisco - Wayne and Gladys Valley Center for Vision — San Francisco

North Carolina

  • Wake Forest Baptist Eye Center — Bermuda Run
  • Duke University - Duke Eye Center — Durham

Florida

  • University of Miami - Bascom Palmer Eye Institute — Miami

Indiana

  • Price Vision Group — Indianapolis

Kansas

  • Kansas City Eye Clinic — Overland Park

Maryland

  • Mid-Atlantic Cornea Consultant — Towson

Massachusetts

  • Massachusetts Eye and Ear — Boston

Michigan

  • University of Michigan - Kellogg Eye Center — Ann Arbor

Trial Details

FieldValue
Enrollment Target 96 participants
Start Date 2025-04-01
Est. Completion 2031-01-01
Phase Phase 2

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06753916

The ClinicalTrials.gov registry entry for NCT06753916 describes a study currently listed as recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 96 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Massachusetts Eye and Ear Infirmary, which has 94 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Corneal Transplant Failure appearing as the primary indexed condition, and to 2 interventions — of which Corneal Donor Tissue with Cross Linking is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06753916 reports 12 study locations spanning 9 distinct geographic areas — top geographies include California, North Carolina, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06753916 about?

NCT06753916 is a clinical study titled "ExCrossV Multi Site Trial for Vascularized High Risk Keratoplasty". The main objective of this study is to determine the safety of Ex Vivo Cross Linking (CXL) of donor corneal tissue in participants who have undergone high-risk penetrating keratoplasty.

What is the current status of trial NCT06753916?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 96 participants. The study started on 2025-04-01. Estimated completion is 2031-01-01.

What conditions does trial NCT06753916 study?

This clinical trial studies the following conditions: Corneal Transplant Failure. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06753916?

The interventions under investigation include: Corneal Donor Tissue with Cross Linking (PROCEDURE), Corneal Donor Tissue without Cross Linking (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06753916?

This trial is sponsored by Massachusetts Eye and Ear Infirmary, which has 94 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06753916 being conducted?

This trial has 12 study locations across California, Florida, Indiana, Kansas, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial