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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02728479
Other study ID # PTA Registry
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 2014
Est. completion date January 2030

Study information

Verified date February 2020
Source Heinrich-Heine University, Duesseldorf
Contact Christian Heiss, MD
Phone +49 211 8118800
Email christian.heiss@med.uni-duesseldorf.de
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Percutaneous transluminal angioplasty (PTA) is a minimally invasive procedure for dilating blood vessels in the treatment of peripheral artery disease.

The aim of this registry is to collect prospectively and systematically clinical research data from patients undergoing PTA. This registry is an open-end observational study to assess the characteristics and outcomes in patients with undergoing PTA.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date January 2030
Est. primary completion date January 2030
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients undergoing PTA

Exclusion Criteria:

- < 18 years

Study Design


Related Conditions & MeSH terms

  • Percutaneous Transluminal Angioplasty

Locations

Country Name City State
Germany Division of Cardiology, Pulmonary Disease and Vascular Medicine Düsseldorf

Sponsors (1)

Lead Sponsor Collaborator
Klinik für Kardiologie, Pneumologie und Angiologie

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Patency rate 6 months
Primary Creatinine level 2 Days after PTA
Secondary Mortality 30 days
Secondary Days of Hospitalization Days of Hospitalization at 12 months 12 months
Secondary Ankle-Brachial Index Clinical Improvement measured by Ankle-Brachial Index 6 months and 12 months
Secondary walking distance Clinical Improvement measured by walking distance 6 months and 12 months
Secondary Restenosis rate Percentage of patients with restenosis at 12 months 12 months
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