Long Term Results of 450 Percutaneous Closures of PDA in a Single Center

Sponsor
Rambam Health Care Campus (Other)
Overall Status
Completed
CT.gov ID
NCT01929733
Collaborator
(none)
450
1
187
2.4

Study Details

Study Description

Brief Summary

Percutaneous closure is one of the methods used to treat, among other congenital heart disorder, Persistent Ductus Arteriosus (PDA) in children and adults. During the years 1998-2013 four hundred and fifty patients were catheterized in the department of pediatric cardiology and congenital heart diseases in Rambam health care campus, using various devices.

In this retrospective research, the investigators analyze data from patients' medical files, to estimate and define the correlation between the patients' demographic and morphologic data to the type and size of chosen closure device.

Aim of study:

To create an algorithm that can be used to choose the proper device for percutaneous closure of the PDA, based on the characteristics of the patient and the PDA type.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The investigators analyze the demographic characteristics of patients before the procedure (Age, gender, weight, height, co-morbidities etc.), the type and characteristics of PDA and the chosen device, success and failure rates of the procedure, and adverse effects.

    The data is taken from patients' medical files - based on medical reports regarding physical examination, blood tests and imaging studies including cineangiograms and echo-doppler studies.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    450 participants
    Time Perspective:
    Retrospective
    Official Title:
    Long Term Results of 450 Percutaneous Closures of PDA in a Single Center
    Study Start Date :
    Jan 1, 1998
    Actual Primary Completion Date :
    Aug 1, 2013
    Actual Study Completion Date :
    Aug 1, 2013

    Outcome Measures

    Primary Outcome Measures

    1. Success of implantation [one day, 10 days and a year after PDA closure and then last check-up exam]

      due to the fact that the research is retrospective and refers to a period of 15 years (1998-2013)and the fact that some patients had a check-up exam from time to time - the investigators have decided to include in this research the last check-up exam as well.

    Secondary Outcome Measures

    1. residual shunt [one day, 10 days and a year after PDA closure and then last check-up exam]

      due to the fact that the research is retrospective and refers to a period of 15 years (1998-2013) and the fact that some patients had a check-up exam from time to time - the investigators have decided to include in this research the last check-up exam as well.

    Other Outcome Measures

    1. Early and late Adverse effects [one day, 10 days and a year after PDA closure and then last check-up exam]

      hemolysis, bleeding, infections ect. due to the fact that the research is retrospective and refers to a period of 15 years (1998-2013)and the fact that some patients had a check-up exam from time to time - the investigators have decided to include in this research the last check-up exam as well.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • All the patients that underwent percutaneous closure of PDA between January 1998 and august 2013 in the department of pediatric cardiology and congenital heart diseases in Rambam health care campus
    Exclusion Criteria:
    • None

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 RAMBAM health care center Haifa Israel 31096

    Sponsors and Collaborators

    • Rambam Health Care Campus

    Investigators

    • Principal Investigator: Moshe Dotan, MD, Rambam Health Care Campus
    • Principal Investigator: Omer Ephrat, Rambam Health Care Campus

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Rambam Health Care Campus
    ClinicalTrials.gov Identifier:
    NCT01929733
    Other Study ID Numbers:
    • 0192-13
    First Posted:
    Aug 28, 2013
    Last Update Posted:
    Aug 28, 2013
    Last Verified:
    Aug 1, 2013
    Keywords provided by Rambam Health Care Campus
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 28, 2013