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NCT04386213

Trial for MicroPort's DCB

Status unknown NA Last updated 13 May 2020
What this trial tests

NA trial testing coronary artery in-stent restenosis in Coronary Artery In-stent Restenosis in 216 participants. Status unknown.

Timeline
1 September 2020
Primary endpoint
1 December 2023
31 July 2025

Quick facts

Lead sponsorShanghai MicroPort Medical (Group) Co., Ltd.
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment216
Start date1 September 2020
Primary completion1 December 2023
Estimated completion31 July 2025

Drugs / interventions tested

Conditions studied

Sponsor

Shanghai MicroPort Medical (Group) Co., Ltd. — full company profile →

Who can join

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

Sponsor's own description

This study is a multicenter, randomized, controlled clinical research and aims to evaluate the safety and efficacy of the paclitaxel drug-coated coronary artery balloon catheter in patients with coronary artery in-stent restenosis compared to seQuent® please paclitaxel drug-coated coronary artery balloon catheter.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Shanghai MicroPort Medical (Group) Co., Ltd. trials

Trials by the same sponsor.

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Data sources for this page

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