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Search / Trial NCT05841914

Multicentre Implementation and Validation of a Molecular Diagnostic for VitreoRetinal Lymphoma

Launched by VINODH KAKKASSERY, MD · Apr 21, 2023

Trial Information

Current as of November 06, 2025

Recruiting

Keywords

Vitreoretinal Lymphoma Primary Cns Lymphoma Improved Detection Molecular Diagnostics Diagnostic Standardisation Health Services Research Prospective Study

ClinConnect Summary

This clinical trial is focused on understanding a type of eye cancer called Vitreoretinal Lymphoma (VRL). Researchers want to learn more about the changes in proteins and genes in different fluids related to the eye, like the aqueous humour and vitreous humour, as well as blood samples. By studying these changes, the goal is to improve the way doctors diagnose and treat this disease. The trial aims to include at least 220 patients and will compare new testing methods with standard procedures to see which is more effective at identifying VRL.

To participate in this study, individuals must be over 18 years old and have a clinical suspicion of VRL that requires a specific eye procedure called vitrectomy. Participants will need to give their written consent to take part. Those who have recently received certain treatments for lymphoma or have specific eye conditions might not be eligible. During the study, participants will be monitored for two years to track their treatment response and any potential recurrence of the disease. This trial is not yet recruiting participants, but it represents an important step toward enhancing the understanding and management of Vitreoretinal Lymphoma.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Clinical suspicion of the presence of VRL with indication for diagnostic vitrectomy. Clinical suspicion is based on the assessment of the treating physicians in the clinics participating in this study.
  • Age over 18 years.
  • Written informed consent to participate in the study.
  • Exclusion Criteria:
  • Systemic chemotherapy for lymphoma within 3 months prior to vitrectomy.
  • Cortisone use within 2 weeks before vitrectomy, macular oedema, posterior synechiae, rubeosis iridis

About Vinodh Kakkassery, Md

Dr. Vinodh Kakkassery, MD, is a distinguished clinical trial sponsor with a robust commitment to advancing medical research and improving patient outcomes. With a strong background in clinical practice and a focus on innovative therapeutic solutions, Dr. Kakkassery leads trials that emphasize rigorous scientific methodologies and ethical standards. His expertise spans various therapeutic areas, contributing to the development of cutting-edge treatments and fostering collaboration within the research community. Dr. Kakkassery's dedication to excellence in clinical trials positions him as a key player in the pursuit of transformative healthcare advancements.

Locations

Lübeck, Schleswig Holstein, Germany

Patients applied

0 patients applied

Trial Officials

Vinodh Kakkassery, PD Dr.med.

Study Chair

University of Luebeck

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported