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Evaluation of safty and efficacy of rotational atherectomy for the treatment of chronic total occlusion lesions

Evaluation of safty and efficacy of rotational atherectomy for the treatment of chronic total occlusion lesions

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-15007610
Enrollment
Unknown
Registered
2015-12-19
Start date
2015-12-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Coronary Artery Disease

Interventions

trail group:rotational atherectomy
control group:predilatation balloon

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) ages between 18 and 90 years old; 2) the ischemic related lesion is chronic total occlusion lesion defined by coronary angiography, TIMI flow is 0; 3) occlusion artery territory exist collerated artery; 4) the guding wire could go through the occlusion lesion.

Exclusion criteria

Exclusion criteria: 1) target lesion is restenosis in stent; 2) target lesion is in vein-grafts; 3) there is moderate to severe dissection after guding wire go through the lsion; 4) the target lesion with extremely tortuous angle; 5) serious arrthymia caused unstable haemodynamic; 6) patients with serious infection; 7) patients with tumor and life expentancy is less than 1 year; 8) patients with activing bleeding; 9) patients with serious renal insufficiency.

Design outcomes

Primary

MeasureTime frame
late lumen loss;

Secondary

MeasureTime frame
operate success;major cardiac event at year 1;major cardiac event at year 2;

Countries

China

Contacts

Public ContactWang Yu
wangyu301@126.com+86 13701246810

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026