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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02887729
Other study ID # GENKYST
Secondary ID
Status Recruiting
Phase N/A
First received August 30, 2016
Last updated September 1, 2016
Start date June 2010

Study information

Verified date August 2016
Source University Hospital, Brest
Contact Yannick Le Meur, MD PhD
Email yannick.lemeur@chu-brest.fr
Is FDA regulated No
Health authority France: Commission nationale de l'informatique et des libertésFrance: Ministère de l'Enseignement supérieur et de la RechercheFrance: Comité consultatif sur le traitement de l'information en matière de recherche dans le domaine de la santé
Study type Observational

Clinical Trial Summary

Genkyst is a regional cohort involving up to nephrologists working in private and public nephrology centers in the West of France. It registers clinical and molecular genetic data of all consenting patients with ADPKD from this area.


Recruitment information / eligibility

Status Recruiting
Enrollment 4000
Est. completion date
Est. primary completion date January 2020
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- ADPKD patients followed in Nephrology centers in the West of France

- Age >17

Exclusion Criteria:

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
France CHU Angers Angers
France AUB Brest Brest
France Centre Nephrologie et Dialyse d Armorique Brest
France CHU Brest Brest
France CH La Roche Sur Yon La Roche sur Yon
France CH Le Mans Le Mans
France ECHO dialyse Le Mans
France AUB Lorient Lorient
France CH Bretagne Sud Lorient
France AUB Morlaix Morlaix
France CHU Nantes Nantes
France CH Niort Niort
France CHU Poitiers Poitiers
France CH Centre Bretagne Pontivy
France AUB Quimper Quimper
France CHI de Cournouaille Quimper
France CHU Rennes Rennes
France ECHO Confluent Reze
France Centre Heliomarin de Roscoff Roscoff
France CH Yves LE FOLL Saint Brieuc
France ECHO Centre Ambulatoire Saint Herblain
France CH Saint Malo Saint Malo
France CH de Saint Nazaire Saint Nazaire
France CHU Tours Tours
France CH Bretagne Atlantique Vannes
France ECHO Vannes Vannes

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Brest

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical description of the patient at the inclusion day No
Secondary Genetic analysis at the inclusion day No
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