Safety, Performance and Usability of BALT Medical Devices: The EVIDENCE Post Marketing Clinical Follow-up Platform. An International, Multicenter, Prospective, and Retrospective Data Collection

Status: Recruiting
Location: See all (12) locations...
Intervention Type: Device
Study Type: Observational
SUMMARY

BALT has designed an electronic platform to continue collecting clinical data as part of the post-marketing clinical follow-up of its devices. This platform is purely exploratory, without hierarchical order of the objectives and associated outcomes.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 2
Healthy Volunteers: f
View:

• Provision of a signed, written and dated informed consent or non-opposition (where applicable)

Locations
Other Locations
France
CHU Angers
RECRUITING
Angers
Chu Bordeaux
RECRUITING
Bordeaux
CHU Grenoble Alpes
RECRUITING
La Tronche
Hôpital Roger Salengro
RECRUITING
Lille
Kremlin Bicêtre - APHP
RECRUITING
Paris
Chu Tours
RECRUITING
Tours
Germany
Halle
RECRUITING
Halle
Spain
Hospital Clinico Universitario San Carlos
TERMINATED
Madrid
Hospital: Fundacion Jimenez Diaz
RECRUITING
Madrid
Unversitario Central de Asturias
RECRUITING
Oviedo
Hospital Universitario Marqués de Valdecilla (HUMV)
RECRUITING
Santander
Hospital Universitario Miguel Servet
NOT_YET_RECRUITING
Zaragoza
Contact Information
Primary
Clinical Affairs Department
Evidence@baltgroup.com
+33 1 39 89 46 41
Time Frame
Start Date: 2021-07-12
Estimated Completion Date: 2041-10
Participants
Target number of participants: 10000
Treatments
BALT medical devices
Authors
Joaquin Medrano
Sponsors
Leads: Balt Extrusion

This content was sourced from clinicaltrials.gov