Registry for patients undergoing percutaneous transluminal angioplasty
Official title: PTA Registry - an Observational Study of Percutaneous Transluminal Angioplasty
Run by Heinrich-Heine University, Duesseldorf · NCT02728479 · Data updated 2026-11-12
This study collects information from patients who are having a minimally invasive procedure called angioplasty to see how well it works and how safe it is for different people with peripheral artery disease.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 1000 (estimated) |
| Sponsor | Heinrich-Heine University, Duesseldorf Academic / other |
| Locations | 1 site (Düsseldorf) |
| Status | Recruiting |
| Started | January 2014 |
| Main results expected | January 2030 |
| Study ends | January 2030 |
| Registry record updated | February 7, 2020 |
| Trial ID | NCT02728479 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this registry are patients who are scheduled to undergo percutaneous transluminal angioplasty.
✕Probably not a fit
Patients under 18 years old will not benefit from this registry.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This registry collects clinical data from patients who are undergoing percutaneous transluminal angioplasty (PTA), a minimally invasive procedure used to treat peripheral artery disease. The study is observational and aims to systematically assess the characteristics and outcomes of these patients. By gathering this data, researchers hope to better understand the effectiveness and safety of PTA in various patient populations.
Why it matters
Potential benefit: If successful, this registry could provide valuable insights that improve treatment strategies for patients with peripheral artery disease.
How similar studies have gone: While this registry approach is common in clinical research, the specific outcomes of PTA have been previously studied, indicating potential for valuable insights.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients undergoing PTA Exclusion Criteria: * \< 18 years
Where it's running
-
Division of Cardiology, Pulmonary Disease and Vascular Medicine
Düsseldorf, Germany Recruiting
Study contacts
- Principal investigator: Christian Heiss, MD — Division of Cardiology, Pulmonary Disease and Vascular Medicine
- Study coordinator: Christian Heiss, MD
- Email: christian.heiss@med.uni-duesseldorf.de
- Phone: +49 211 8118800
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.