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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03025685
Other study ID # TRUST
Secondary ID
Status Completed
Phase N/A
First received January 12, 2017
Last updated December 24, 2017
Start date September 2016
Est. completion date December 2016

Study information

Verified date December 2017
Source Meshalkin Research Institute of Pathology of Circulation
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Adequate support is required for challenging percutaneous coronary interventions (PCI). The "TransRadial Ultra Support Technique" (TRUST technique) is a new support technique that provides active support by deep pass of the coronary wire into the heart cavities (left ventricle-LV, right ventricle-RV) or aorta.


Recruitment information / eligibility

Status Completed
Enrollment 54
Est. completion date December 2016
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Subjects singed informed consent form

- Subjects eligible for percutaneous coronary intervention

Exclusion Criteria:

- Age <18 years or >75 years

- Subject has a platelet count < 100,000 cells/mm3 or > 700,000 cells/mm3.

- Known non-adherence to double anti-platelet therapy (DAPT)

- LVEF <30%

- Continuing bleeding

- Acute coronary syndrome (ST-elevation Myocardial infarction)

- Pregnancy

Study Design


Intervention

Procedure:
TRUST technique
A soft hydrophilic wire easily pass through the invisible small vessels in the distal parts of a coronary artery into a heart cavity. It is necessary to pass a wire softly and forward as deep as possible. Quite often the wire goes through the left ventricle to aorta arch, and sometimes distal soft tip can be visible in a descending aorta. Thus the stiffest part of the wire become staying on all length of artery, straightening bends and giving the maximum support. After that balloons and stents can be delivered more easily
Anchoring Technique
A standard endovascular technique of coronary wire support improvement
Coronary stenting
A standard endovascular procedure of percutaneous coronary intervention with coronary stenting

Locations

Country Name City State
Russian Federation State Research Institute of CIrculation Pathology Novosibirsk

Sponsors (1)

Lead Sponsor Collaborator
Meshalkin Research Institute of Pathology of Circulation

Country where clinical trial is conducted

Russian Federation, 

Outcome

Type Measure Description Time frame Safety issue
Primary Procedural success Device success without the occurrence of in-hospital MACCE 1 week after PCI
Primary Device success Achievement of a final residual diameter stenosis <20% and a TIMI 3 flow in the target vessel Intraoperative
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