Working...
ClinicalTrials.gov
ClinicalTrials.gov Menu
Trial record 1 of 89 for:    Recruiting, Not yet recruiting, Available Studies | Angioplasty
Previous Study | Return to List | Next Study

Percutaneous Transluminal Angioplasty Registry

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT02728479
Recruitment Status : Recruiting
First Posted : April 5, 2016
Last Update Posted : January 9, 2019
Sponsor:
Information provided by (Responsible Party):
Klinik für Kardiologie, Pneumologie und Angiologie, Heinrich-Heine University, Duesseldorf

Brief 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.


Condition or disease
Percutaneous Transluminal Angioplasty

Layout table for study information
Study Type : Observational [Patient Registry]
Estimated Enrollment : 1000 participants
Observational Model: Cohort
Time Perspective: Prospective
Target Follow-Up Duration: 12 Months
Official Title: PTA Registry - an Observational Study of Percutaneous Transluminal Angioplasty
Study Start Date : January 2014
Estimated Primary Completion Date : January 2020
Estimated Study Completion Date : January 2020

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Angioplasty




Primary Outcome Measures :
  1. Patency rate [ Time Frame: 6 months ]
  2. Creatinine level [ Time Frame: 2 Days after PTA ]

Secondary Outcome Measures :
  1. Mortality [ Time Frame: 30 days ]
  2. Days of Hospitalization [ Time Frame: 12 months ]
    Days of Hospitalization at 12 months

  3. Ankle-Brachial Index [ Time Frame: 6 months and 12 months ]
    Clinical Improvement measured by Ankle-Brachial Index

  4. walking distance [ Time Frame: 6 months and 12 months ]
    Clinical Improvement measured by walking distance

  5. Restenosis rate [ Time Frame: 12 months ]
    Percentage of patients with restenosis at 12 months



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients undergoing PTA
Criteria

Inclusion Criteria:

  • Patients undergoing PTA

Exclusion Criteria:

  • < 18 years

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02728479


Contacts
Layout table for location contacts
Contact: Christian Heiss, MD +49 211 8118800 christian.heiss@med.uni-duesseldorf.de
Contact: Rabea Wagstaff, BSc., M.A. +49 211 8118800 rabea.wagstaff@med.uni-duesseldorf.de

Locations
Layout table for location information
Germany
Division of Cardiology, Pulmonary Disease and Vascular Medicine Recruiting
Düsseldorf, Germany, 40225
Contact: Christian Heiss, MD         
Sub-Investigator: Yvonne Heinen, MD         
Sub-Investigator: Nana-Yaw Bimpong-Buta, MD         
Sub-Investigator: Lucas Busch, MD         
Principal Investigator: Christian Heiss, MD         
Sponsors and Collaborators
Klinik für Kardiologie, Pneumologie und Angiologie
Investigators
Layout table for investigator information
Principal Investigator: Christian Heiss, MD Division of Cardiology, Pulmonary Disease and Vascular Medicine

Additional Information:

Layout table for additonal information
Responsible Party: Klinik für Kardiologie, Pneumologie und Angiologie, Heinrich-Heine University, Duesseldorf
ClinicalTrials.gov Identifier: NCT02728479     History of Changes
Other Study ID Numbers: PTA Registry
First Posted: April 5, 2016    Key Record Dates
Last Update Posted: January 9, 2019
Last Verified: January 2019