Registry for infants with Retinopathy of Prematurity in Europe
European Disease Registry on Retinopathy of Prematurity (ROP)
This study is collecting information about infants with Retinopathy of Prematurity across Europe to better understand how the condition varies and how it's treated.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 3000 (estimated) |
| Sex | All |
| Sponsor | University Medicine Greifswald Academic / other |
| Locations | 59 sites (Salzburg and 58 other locations) |
| Trial ID | NCT04939571 on ClinicalTrials.gov |
What this trial studies
The EU-ROP registry is a multicenter observational study across Europe aimed at collecting clinical data on infants treated for Retinopathy of Prematurity (ROP). This registry will gather information on the clinical features, treatment patterns, and long-term outcomes of ROP in various European countries without any specific interventions. The study seeks to document the natural history of the disease and variations in its presentation among different populations. By compiling this data, the registry aims to enhance understanding and management of ROP.
Who should consider this trial
Good fit: Ideal candidates for this registry are infants diagnosed with ROP requiring treatment as per national guidelines.
Not a fit: Patients whose parents or legal guardians do not consent to the documentation and storage of personal data will not benefit from this registry.
Why it matters
Potential benefit: If successful, this registry could improve the understanding of ROP and inform better treatment strategies for affected infants.
How similar studies have performed: Other observational registries have successfully contributed to the understanding of similar conditions, suggesting that this approach could yield valuable insights.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * ROP requiring treatment according to the respective national ROP screening and treatment guidelines Exclusion Criteria: * Denial or absence of consent for documentation and electronic storage of personal data by parents or legal guardians
Where this trial is running
Salzburg and 58 other locations
- University Eye Hospital Salzburg — Salzburg, Austria (Recruiting)
- University Hospital Saint George — Plovdiv, Bulgaria (Recruiting)
- Acibadem City Clinic Tokuda Hospital — Sofia, Bulgaria (Recruiting)
- University Eye Hospital Alexandrovska — Sofia, Bulgaria (Recruiting)
- University Eye Hospital Tartu — Tartu, Estonia (Recruiting)
- Hospital Rothschild — Paris, France (Recruiting)
- University Eye Hospital — Aachen, Germany (Recruiting)
- University Eye Hospital Helios — Berlin, Germany (Recruiting)
- University Eye Hospital Vivantes — Berlin, Germany (Recruiting)
- University Eye Hospital Bonn — Bonn, Germany (Recruiting)
- Braunschweig Muncipal Hospital — Braunschweig, Germany (Recruiting)
- University Eye Hospital — Chemnitz, Germany (Recruiting)
- University Eye Hospital — Cologne, Germany (Recruiting)
- Carl-Thiem University Hospital Cottbus — Cottbus, Germany (Recruiting)
- University Eye Hospital — Düsseldorf, Germany (Recruiting)
- University Eye Hospital — Freiburg im Breisgau, Germany (Recruiting)
- University Eye Hospital Fulda — Fulda, Germany (Recruiting)
- University Eye Hospital Gießen — Giessen, Germany (Recruiting)
- University Eye Hospital — Göttingen, Germany (Recruiting)
- University Eye Hospital — Greifswald, Germany (Recruiting)
- University Eye Hospital — Hamburg, Germany (Recruiting)
- University Eye Hospital Hannover — Hanover, Germany (Recruiting)
- Facharztpraxis für Augenheilkunde — Ludwigshafen, Germany (Recruiting)
- University Eye Hospital — Lübeck, Germany (Recruiting)
- Ludwig-Maximilins-University Munich — Munich, Germany (Not_yet_recruiting)
- Augenzentrum am St. Franziskus-Hospital — Münster, Germany (Recruiting)
- University Eye Hospital — Münster, Germany (Recruiting)
- Nuremberg South Hospital — Nuremberg, Germany (Recruiting)
- Ernst-von-Bergmann Hospital — Potsdam, Germany (Recruiting)
- University Eye Hospital — Regensburg, Germany (Recruiting)
- University Eye Hospital — Tübingen, Germany (Recruiting)
- University Eye Hospital Ulm — Ulm, Germany (Recruiting)
- P&A Kyriakou Athens Children Hospital — Athens, Greece (Recruiting)
- Department of Ophthalmology University Hospital of Larissa — Larissa, Greece (Recruiting)
- Aristotle University of Thessaloniki — Thessaloniki, Greece (Recruiting)
- University Clinical Center of Kosovo — Pristina, Kosovo (Recruiting)
- Medical University of Bialystok Children's Clinical Hospital — Bialystok, Poland (Recruiting)
- University Hospital in Bydgoszcz — Bydgoszcz, Poland (Recruiting)
- University Hospital in Zabrze Silesia — Katowice, Poland (Recruiting)
- Prof. Dr. Stanislaw Popowski Regional Specialized Children's Hospital — Olsztyn, Poland (Recruiting)
- University of Medical Sciences Poznan — Poznan, Poland (Recruiting)
- Children's Memorial Health Institute Warsaw — Warsaw, Poland (Recruiting)
- Biomédica de Málaga y Plataforma en Nanomedicina — Málaga, Spain (Recruiting)
- University and Polytechnic Hospital La Fe — Valencia, Spain (Recruiting)
- University Eye Hospital Genève — Geneva, Switzerland (Recruiting)
- University Eye Hospital Cukurova — Adana, Turkey (Türkiye) (Recruiting)
- Etlik Zübeyde Hanim Women's Health Education and Research Hospital — Ankara, Turkey (Türkiye) (Recruiting)
- Hacettepe University Children's Hospital — Ankara, Turkey (Türkiye) (Recruiting)
- University Eye Hospital Ankara — Ankara, Turkey (Türkiye) (Recruiting)
- University Eye Hospital Baskent — Ankara, Turkey (Türkiye) (Recruiting)
+9 more sites — see ClinicalTrials.gov for the full list.
Study contacts
- Principal investigator: Andreas Stahl, Professor — Department of Ophthalmology, University Medicine Greifswald
- Study coordinator: Andreas Stahl, Professor
- Email: andreas.stahl@med.uni-greifswald.de
- Phone: +49 3834 86
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.