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NCT03541577: SUPREME

Sensor-equipped Ultrathin Pressure Microcatheter Versus Pressure Wire for FFR Measurement

Completed Last updated 27 May 2022
What this trial tests

trial testing TruePhysioTM Microcatheter in Coronary Artery Disease in 242 participants. Completed in 31 January 2019.

Timeline
19 June 2018
Primary endpoint
31 January 2019
31 January 2019

Quick facts

Lead sponsorInsight Lifetech Co., Ltd.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment242
Start date19 June 2018
Primary completion31 January 2019
Estimated completion31 January 2019
Sites4 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

Insight Lifetech Co., Ltd.

Who can join

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

Sponsor's own description

TruePhysioTM Sensor-equipped Ultrathin Pressure Microcatheter (referred to as TruePhysioTM Microcatheter below) is a novel device for evaluating the functional significance of coronary stenosis. This study will compare the differences, if any, between the coronary fractional flow reserve (FFR) measured by the TruePhysioTM Microcatheter and the Pressure Wire.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Coronary Artery Disease

Currently open trials in the same condition.

Other Insight Lifetech Co., 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/NCT03541577.

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