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NCT04823663: SOCRATES

BoStOn SCientific Rhythm MAnagemenT REgiStry (SOCRATES)

Recruiting now Last updated 23 March 2026
What this trial tests

trial testing Implant in Cardiac Disease in 12,500 participants. Currently enrolling.

Timeline
31 March 2021
Primary endpoint
31 December 2030
31 December 2030

Quick facts

Lead sponsorBoston Scientific Corporation
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment12,500
Start date31 March 2021
Primary completion31 December 2030
Estimated completion31 December 2030
Sites26 locations across France, Italy, Greece, Belgium, Ireland, United Kingdom, Germany, Israel

Drugs / interventions tested

Conditions studied

Sponsor

Boston Scientific Corporation — full company profile →

Who can join

Eligibility, any sex, with Cardiac Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

SOCRATES is part of Boston Scientific's (BSC) Post-market surveillance system. The implementation of such systems is mandatory per local regulations such as the Regulation '(EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices' or short Medical Device Regulation (MDR). The SOCRATES design is therefore based on the BSC's commitment as well as external regulatory requirements to proactively and systematically gather, record and analyze relevant data on the quality, performance and safety of devices throughout their entire lifetime.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Implant

Trials testing the same drug.

Other recruiting trials for Cardiac Disease

Currently open trials in the same condition.

Other Boston Scientific Corporation 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/NCT04823663.

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