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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04011527
Other study ID # SK 111 -- 168/11
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 25, 2002
Est. completion date December 31, 2032

Study information

Verified date June 2022
Source Segeberger Kliniken GmbH
Contact Abdelhakim Allali, MD
Phone +4945512802
Email allali.abdelhakim@gmail.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

A Prospective Follow-up Assessment in Bad Segeberg with Patients undergoing a Rotational Atherectomy in Coronary Lesion/s


Description:

A prospective single center registry including all patients treated with Rotational Atherectomy in Coronary Lesion/s at the Heart Center, Bad Segeberg, Germany. Patients undergo a routine clinical follow-up schedule, including a long-term follow-up.


Recruitment information / eligibility

Status Recruiting
Enrollment 1500
Est. completion date December 31, 2032
Est. primary completion date December 31, 2030
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - All patients undergoing a rotational atherectomy of coronary lesion/s Exclusion Criteria: - None

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Rotational Atherectomy in Coronary Lesion/s


Locations

Country Name City State
Germany Herzzentrum Segeberger Kliniken GmbH Bad Segeberg

Sponsors (1)

Lead Sponsor Collaborator
Segeberger Kliniken GmbH

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of in-hospital and long-term cardiovascular adverse events in percent Peri-procedural events and in-hospital cardiovascular events and long-term cardiovascular events (bleeding, peripheral and coronary vascular complication, stroke, myocardial infarction, stent thrombosis, revascularization, death) 2 years
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