Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06491615 · ClinicalTrials.gov registry record

National Ophthalmic Genotyping and Phenotyping Network (eyeGENE (Registered Trademark)), Stage 3 - Expansion of DNA and Data Repositories for Rare Inherited Ophthalmic Diseases

A clinical trial of Aniridia and Corneal Dystrophy, sponsored by National Eye Institute (NEI).

Recruiting
Registry status
1,000
Enrollment target
2
Study locations

NCT06491615: Recruiting study of Aniridia and Corneal Dystrophy, sponsored by National Eye Institute (NEI).

NCT06491615 is a study of Aniridia and Corneal Dystrophy that is actively recruiting participants, run by National Eye Institute (NEI). The registered enrollment target is 1,000 participants. The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06491615, a study of Aniridia and Corneal Dystrophy, is actively recruiting participants, sponsored by National Eye Institute (NEI).

RECRUITING
Registry status
1,000 participants
Enrollment target
2
Study locations

Study Summary

Background: The eyeGENE (Registered Trademark) program is a research resource for inherited eye conditions which includes genotypic and phenotypic data, imaging, and a corresponding biobank of DNA samples from people with a variety of eye diseases. Since 2007 this registry has been helping researchers learn more about the genetic sources for many inherited eye diseases. These findings helped them create better treatments. Now researchers want to expand eyeGENE (Registered Trademark) to include more people for certain eye diseases. Objective: To collect information and DNA samples for the study of eye diseases. * Primary objective --To expand the current eyeGENE (Registered Trademark) data repository with targeted participant accrual * Secondary objectives * To enhance recruitment for clinical trials and investigations in inherited eye diseases * To establish genotype-phenotype correlations for rare eye diseases Eligibility: People of any age with certain eye diseases. These can include aniridia; Best disease; blue-cone monochromacy; corneal dystrophy; and disorders of pigmentation, such as albinism. Relatives unaffected by the eye disease of interest may also be needed. Design: Researchers will select participants based on their diagnosis. The data may include images and test results from eye exams. Participants will provide a sample of saliva. They will receive a kit with written instructions. They will spit in a tube and mail it to the NIH. Participants may be asked to provide a blood sample. The blood may be drawn at the NIH or at a local clinic. The eyeGENE (Registered Trademark) repository will offer researchers data about the participants eye conditions. The data may include pictures of their eyes, results of the genetic testing, and history of other diseases. Researchers will be able to see data such as age and gender, but they will not see names, dates of birth, or contact information.

Primary Outcome

To expand the current eyeGENE data repository with targeted participant accrual.

Study Locations (2)

Maryland

  • National Eye Institute (NEI) - Bethesda
  • National Institutes of Health Clinical Center - Bethesda

Trial Details

FieldValue
Enrollment Target 1,000 participants
Start Date 2024-07-12
Est. Completion 2054-06-27
National Eye Institute (NEI)

221 total trials

What NCT06491615 shows while recruiting

NCT06491615 is an observational study that tracks outcomes without assigning an intervention. Its 1,000 participants enrollment target places it among the larger protocols in the corpus.

The record links to 7 conditions, with Aniridia appearing as the primary indexed condition, and to 0 interventions.

NCT06491615 reports a single indexed study location in Maryland.

Frequently Asked Questions

What is clinical trial NCT06491615 about?

NCT06491615 is a clinical study titled "National Ophthalmic Genotyping and Phenotyping Network (eyeGENE (Registered Trademark)), Stage 3 - Expansion of DNA and Data Repositories for Rare Inherited Ophthalmic Diseases". Background: The eyeGENE (Registered Trademark) program is a research resource for inherited eye conditions which includes genotypic and phenotypic data, imaging, and a corresponding biobank of DNA samples from people with a variety of eye diseases. Since 2007 this registry has been helping research...

What is the current status of trial NCT06491615?

This trial is currently recruiting. The enrollment target is 1,000 participants. The study started on 2024-07-12. Estimated completion is 2054-06-27.

What conditions does trial NCT06491615 study?

This clinical trial studies the following conditions: Aniridia, Corneal Dystrophy, Best Disease, Albinism, Inherited Ophthalmic Diseases.

Who is sponsoring clinical trial NCT06491615?

This trial is sponsored by National Eye Institute (NEI), which has 221 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06491615 being conducted?

This trial has 2 study locations across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Aniridia

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00018044 · 1,000 participants

    Study of Mycobacterial Infections

  • NCT01036581 · 1,000 participants · NA

    Advanced Functional and Structural MRI Techniques for Neuropharmacological Imaging

  • NCT01192048 · 1,000 participants

    Genetics of Congenital Heart Disease

  • NCT01553214 · 1,000 participants · Phase 4

    Improving White Blood Cell Collection From Healthy Donors

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06491615, the US trial registry maintained by the National Library of Medicine. NCT06491615 (large enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.