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NCT02588430Withdrawn

PMCF Study for Partial Vision Restoration Using the Subretinal Implant RETINA IMPLANT Alpha AMS

Post-Market Clinical Follow-up Study for Partial Vision Restoration Using the Subretinal Implant RETINA IMPLANT Alpha AMS

Source: ClinicalTrials.gov · Last updated 19 Apr 2019

Brief summary (registry, in English)

This study is a post-market clinical follow-up (PMCF) study to monitor the safety, lifetime and efficacy of patients using the CE-certified RETINA IMPLANT Alpha AMS.

Status (registry)
Withdrawn
Study type
Observational
Enrollment
0 (actual)
First submitted
30 Sept 2014
Start date
Mar 2019
Primary completion date
Dec 2029
Lead sponsor
Retina Implant AG
NCT number
NCT02588430

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • none

Who the study is looking for

  • Patients who received a RETINA IMPLANT Alpha AMS.
  • Patients willing and able to give written informed consent.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Katharinenhospital StuttgartStuttgartGermanyUnknown status

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This page is information, not medical advice. Discuss any trial with your doctor.