Actively Recruiting

Age: 18Years +
All Genders
NCT05841914

Multicentre Implementation and Validation of a Molecular Diagnostic for VitreoRetinal Lymphoma

Led by Vinodh Kakkassery, MD · Updated on 2025-07-23

220

Participants Needed

1

Research Sites

278 weeks

Total Duration

On this page

Sponsors

V

Vinodh Kakkassery, MD

Lead Sponsor

U

University Hospital Tuebingen

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this observational study is to gain new insights into the changes in proteins, genes and other molecular biological substances in the aqueous humour, vitreous humour, blood serum and, in rare cases, retina/choroid samples in patients with ocular lymphoma disease. The hope is that this will expand the understanding of the mechanisms of the disease and thus contribute to improved and simplified diagnosis and treatment strategies in the future. The aim is the inclusion of at least 220 patients during the study period. The main questions it aims to answer are: * to evaluate the diagnostic quality of extended molecular diagnostics (based on standard work-up) of vitreous samples for the specific VitreoRetinalLymphoma (a type of ocular lymphoma disease) diagnosis in comparison to standard work-up alone. * To monitor VRL patients as part of regular tumour follow-up over a period of 24 months to determine the value of biomarkers with regard to treatment response and development of recurrence in the eye. Similarly, the vitritis patients are followed up by telephone every six months for a period of 24 months, during which questions of any interim occurrence of a VRL or other cancerous tumors are asked according to a defined catalogue of questions.

CONDITIONS

Official Title

Multicentre Implementation and Validation of a Molecular Diagnostic for VitreoRetinal Lymphoma

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Clinical suspicion of vitreoretinal lymphoma (VRL) with recommendation for diagnostic vitrectomy
  • Age over 18 years
  • Provided written informed consent to participate in the study
Not Eligible

You will not qualify if you...

  • Received systemic chemotherapy for lymphoma within 3 months before vitrectomy
  • Used cortisone within 2 weeks before vitrectomy
  • Presence of macular oedema
  • Presence of posterior synechiae
  • Presence of rubeosis iridis

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Clinic of Schleswig-Holstein

Lübeck, Schleswig-Holstein, Germany, 23538

Actively Recruiting

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Research Team

L

Liv Dollmann

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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