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NCT02857894: ATM

Genetic Factors of Idiopathic Polypoidal Vasculopathies in the ATM Gene (Ataxia Telangiectasia Mutated)

Terminated Last updated 29 October 2018
What this trial tests

trial in Choroidal Neovascularization in 7 participants. Terminated before completion.

Timeline
5 November 2015
Primary endpoint
23 October 2018
23 October 2018

Quick facts

Lead sponsorFondation Ophtalmologique Adolphe de Rothschild
StatusTerminated
Study typeOBSERVATIONAL
Enrollment7
Start date5 November 2015
Primary completion23 October 2018
Estimated completion23 October 2018
Sites1 location across France

Conditions studied

Sponsor

Fondation Ophtalmologique Adolphe de Rothschild — full company profile →

Who can join

18 and older, any sex, with Choroidal Neovascularization. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Polypoidal choriodal vasculopathy (PCV) is an ophthalmologic disease, characterized by vascular abnormalities of the walls of small choroidal vessels, reproducing the specific aspect of polyps (cluster aspect). PCV is one of the "boundary-forms" of age related macular degeneration. These vasculopathies can be idiopathic. Following the radiotherapy treatments of active and occult-typed neovessels in Age-Related Macular Degeneration (ARMD), 10% of the patients would present typical polypoidal vasculopathic lesions. These polypoidal secondary lesions have been induced by radiotherapy treatment and may show an increased sensibility to radiation in these patients. Such an increase of radiosensibility is noticed in ataxia telangiectasia syndrome, in relation to the ATM gene mutations. The secondary or idiopathic polypoidal vasculopathic lesions are to be brought closer to telangiectasias in Ataxia Telangiectasia. Considering the iatrogenic component of radiotherapy in the secondary forms of ataxia telangiectasia, it seems legitimate to search for predisposing variants to polypoidal vasculopathies in the ATM gene. Considering the frequency of PCV worldwide, it seems important to identify the predisposing genetic factors of the ATM gene. These biomarkers to the pathology might enable us to offer prevention (reinforced protection against radiations, including light) and to develop therapeutics (recruitment of other kinases, ATM's partners, in the stability and cellular control of DNA).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Choroidal Neovascularization

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Data sources for this page

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