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NCT03901391: RU-RP

Prospective Open Clinical and Genetic Study of Patients With Retinitis Pigmentosa

Completed Last updated 20 May 2022
What this trial tests

trial testing Whole Exome Sequencing in Retinitis Pigmentosa in 130 participants. Completed in 20 October 2020.

Timeline
26 March 2019
Primary endpoint
19 October 2020
20 October 2020

Quick facts

Lead sponsorSensor Technology for Deafblind
StatusCompleted
Study typeOBSERVATIONAL
Enrollment130
Start date26 March 2019
Primary completion19 October 2020
Estimated completion20 October 2020
Sites2 locations across Russia

Drugs / interventions tested

Conditions studied

Sponsor

Sensor Technology for Deafblind

Who can join

Adults 6 to 65, any sex, with Retinitis Pigmentosa or Usher Syndromes. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is aimed to characterize Russian population of Retinitis Pigmentosa

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Abstracts from the 53rd European Society of Human Genetics (ESHG) Conference: e-Posters.
    · 2020 · cited 4× · PMID 33262486 · DOI 10.1038/s41431-020-00741-5

Verify or expand the search:

Other trials of Whole Exome Sequencing

Trials testing the same drug.

Other recruiting trials for Retinitis Pigmentosa

Currently open trials in the same condition.

Other Sensor Technology for Deafblind trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03901391.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing