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NCT03716011

A Postmarket Clinical Trial for EXCROSSAL Stent in CAD Patients With 3-month DAPT or 12-month DAPT

Status unknown NA Last updated 23 October 2018
What this trial tests

NA trial testing EXCROSSAL in Coronary Artery Disease in 2,700 participants. Status unknown.

Timeline
20 December 2018
Primary endpoint
20 December 2021
20 December 2025

Quick facts

Lead sponsorJW Medical Systems Ltd
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment2,700
Start date20 December 2018
Primary completion20 December 2021
Estimated completion20 December 2025
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

JW Medical Systems Ltd

Who can join

Adults 18 to 75, any sex, with Coronary Artery Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

1. Prospective, randomized, multicenter clinical study 2. This is a post-marketing clinical study to evaluate whether it will affect the safety event when it is used in different treatment ways. Adopting non - inferiority design, 2700 cases were enrolled. 3. EDC system (eCRF electronic data collection system) 4. Follow-up points: 30 days,3 months, 12 months, 24 months, 36 months, 48 months and 60 months after the operation;

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Coronary Artery Disease

Currently open trials in the same condition.

Other JW Medical Systems Ltd 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/NCT03716011.

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