Glider PTCA Balloon Catheter Registry

Registry for PCI With the TriReme Medical, Inc. Glider(TM) PTCA Balloon Catheter

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01184352

Enrollment

125

Registered

2010-08-18

Start date

2010-07-31

Completion date

2012-09-30

Last updated

2012-12-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Disease

Brief summary

The objective of this Registry is to demonstrate the utility of the Glider PTCA Balloon Catheter for crossing during the treatment of coronary artery disease.

Interventions

DEVICETriReme Medical, Inc. Glider(TM) PTCA Balloon Catheter

Percutaneous Coronary Interventions performed with the Glider PTCA Balloon Catheter

Study design

Observational model

CASE_ONLY

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Patients undergoing PCI who are at least 18 years old * PCI procedure included the use of at least one Glider PTCA Balloon Catheter * Patient has been informed, in accordance with local requirements, that their data will be used in the Glider Registry

Exclusion criteria

* N/A

Design outcomes

Primary

Measure	Time frame	Description
Technical Success	average of 1 hour	Percentage of lesions successfully crossed among those attempted with the Glider PTCA Balloon Catheter as assesed during procedure.

Secondary

Measure	Time frame	Description
Procedure Success	average of 2 days	Percentage of patients treated with at least one Glider PTCA Balloon Catheter having \<50% residual diameter stenosis, or TIMI 3 flow if at a bifurcation side branch, without the development of in-hospital MACE (Major Adverse Cardiac Event).

Countries

Germany, United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026