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Clinical trials for Retinal

The European Union Clinical Trials Register   allows you to search for protocol and results information on:
  • interventional clinical trials that were approved in the European Union (EU)/European Economic Area (EEA) under the Clinical Trials Directive 2001/20/EC
  • clinical trials conducted outside the EU/EEA that are linked to European paediatric-medicine development

    • EU/EEA interventional clinical trials approved under or transitioned to the Clinical Trial Regulation 536/2014 are publicly accessible through the
    Clinical Trials Information System (CTIS).

    The EU Clinical Trials Register currently displays   44339   clinical trials with a EudraCT protocol, of which   7369   are clinical trials conducted with subjects less than 18 years old.   The register also displays information on   18700   older paediatric trials (in scope of Article 45 of the Paediatric Regulation (EC) No 1901/2006).

    Phase 1 trials conducted solely on adults and that are not part of an agreed paediatric investigation plan (PIP) are not publicly available (see Frequently Asked Questions ).  
     
    Examples: Cancer AND drug name. Pneumonia AND sponsor name.
    How to search [pdf]
    Search Tips: Under advanced search you can use filters for Country, Age Group, Gender, Trial Phase, Trial Status, Date Range, Rare Diseases and Orphan Designation. For these items you should use the filters and not add them to your search terms in the text field.
    Advanced Search: Search tools
     
    Query did not match any clinical trials.
    These are paediatric studies completed by 26 January 2007, in respect of products authorised in the Community (Article 45 of the Paediatric Regulation (EC) No 1901/2006).
    Note: Advanced search filters for country, trial phase, gender, rare disease, IMP with orphan designation in the indication and age ranges of in-utero, adult or elderly do not apply to these records.
    Study title: Subramaniam, R., B. Ghai, et al."A comparison of intravenous ketoprofen versus pethidine on peri-operative analgesia and post-operative nausea and vomiting in paediatric vitreoretinal surgery."; J Postgrad Med 49(2): 123-6, 2003.
    Active substance: KETOPROFEN
    Study summary document link (including results):
    View full study record
    Document reference: 30884
    Study title: Long-term results of laser treatment for retinal angiomatosis in von Hippel-Lindau disease. Schmidt D, Natt E, Neumann HP. Eur J Med Res. 2000 Feb 28;5(2):47-58.
    Active substance: FLUORESCEIN
    Study summary document link (including results): Long-term results of laser treatment for retinal angiomatosi.pdf
    View full study record
    Document reference: 28245
    Study title: Morel C, Metge F, Roman S, Scheer S, Larricart P, Monin C et al. [Acute retinal necrosis: clinical presentation, treatment, and prognosis in a series of 22 patients]. [French]. Journal Francais d Opthalmologie 2004; 27(1):7-13.Morel C, Metge F, Roman S, Scheer S, Larricart P, Monin C et al. [Acute retinal necrosis: clinical presentation, treatment, and prognosis in a series of 22 patients]. [French]. Journal Francais d Opthalmologie 2004; 27(1):7-13.
    Active substance: FOSCARNET
    Study summary document link (including results): Morel C et al 2004.pdf
    View full study record
    Document reference: 28589
    Study title: The Studies of Ocular Complications of AIDS (SOCA) Research Group in Collaboration with the AIDS Clinical Trials Group. Rhegmatogenous retinal detachment in patients with cytomegalovirus retinitis: the Foscarnet-Ganciclovir Cytomegalovirus Retinitis Trial. American Journal of Opthalmology 1997; 124(1): 61-70.The Studies of Ocular Complications of AIDS (SOCA) Research Group in Collaboration with the AIDS Clinical Trials Group. Rhegmatogenous retinal detachment in patients with cytomegalovirus retinitis: the Foscarnet-Ganciclovir Cytomegalovirus Retinitis Trial. American Journal of Opthalmology 1997; 124(1): 61-70.
    Active substance: Foscarnet
    Study summary document link (including results): SOCA studies 1997 (a).pdf
    View full study record
    Document reference: 39654
    Study title: Tran TH, Stanescu D, Caspers-Velu L, Rozenberg F, Liesnard C, Gaudric A et al. Clinical characteristics of acute HSV-2 retinal necrosis. [Review] [42 refs]. American Journal of Ophthalmology 2004; 137(5):872-879.Tran TH, Stanescu D, Caspers-Velu L, Rozenberg F, Liesnard C, Gaudric A et al. Clinical characteristics of acute HSV-2 retinal necrosis. [Review] [42 refs]. American Journal of Ophthalmology 2004; 137(5):872-879.
    Active substance: FOSCARNET
    Study summary document link (including results): Tran TH et al 2004.pdf
    View full study record
    Document reference: 28591
    Study title: Follow-Up Screening to Investigate the Occurrence of Long-Term Retinal Effects in Children Exposed to Vigabatrin Treatment and in Subjects Exposed to Vigabatrin In Utero.
    Active substance: VIGABATRIN
    Study summary document link (including results): Vigabatrin-Study 3.pdf
    View full study record
    Document reference: 39389
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    The status and protocol content of GB trials is no longer updated since 1 January 2021. For the UK, as of 31 January 2021, EU Law applies only to the territory of Northern Ireland (NI) to the extent foreseen in the Protocol on Ireland/NI. Legal notice
    As of 31 January 2023, all EU/EEA initial clinical trial applications must be submitted through CTIS . Updated EudraCT trials information and information on PIP/Art 46 trials conducted exclusively in third countries continues to be submitted through EudraCT and published on this website.

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