CompletedNot applicableNCT04793100
Spontaneous Retinal Artery Pulses (SPARs) as a Prognostic Determinant of Central Retinal Vein Occlusions (CRVO) in Patients With or Without Intravitreal Aflibercept Injections
Studying Central retinal vein occlusion
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Fondation Ophtalmologique Adolphe de Rothschild
- Principal Investigator
- Martine MAUGET FAYSSE, MDHôpital Fondation A. de Rothschild
- Intervention
- Ophthalmologic exam at inclusion and 12 months after CRVO(other)
- Enrollment
- 60 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2021 – 2025
Study locations (3)
- Centre Pôle Vision du Val d'ouest, Lyon, Écully, France
- Hôpital Fondation A. de Rothschuld, Paris, France
- Centre médical et chirurgical de la rétine Strasbourg, Strasbourg, France
Collaborators
Bayer
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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