Prognosis and Integrative Assessment of Aortic Coarctation Patients in China

Sponsor
Beijing Institute of Heart, Lung and Blood Vessel Diseases (Other)
Overall Status
Recruiting
CT.gov ID
NCT04011956
Collaborator
Beijing Anzhen Hospital (Other), Bayi Children's Hospital Affiliated to PLA Army General Hospital, China (Other), Capital Institute of Pediatrics, China (Other)
300
1
58
5.2

Study Details

Study Description

Brief Summary

This is a systemic research of Chinese aortic coarctation patients, aiming to determine risk factors and serial biomarkers of aortic coarctation in prognosis.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The goal is to determine how much the left ventricle remodeling pre-operation and how it changes in the following-up duration after surgery, so does in the blood pressure and heart function. Risk factors associated with complications and prognosis are investigated and analyzed. Identification of novel biomarkers is needed to help predicting the prognosis, such as the left ventricle anti-remodeling, heart function and blood pressure improvement, as well as the exercise tolerance post-operation. The findings of this study will help the investigators developping new tests to monitor affected patients and optimize the operation as well as the follow-up procedure.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    300 participants
    Observational Model:
    Cohort
    Time Perspective:
    Other
    Official Title:
    Prognosis and Integrative Assessment of Aortic Coarctation Patients in CHINA
    Actual Study Start Date :
    Mar 1, 2019
    Anticipated Primary Completion Date :
    Dec 31, 2022
    Anticipated Study Completion Date :
    Dec 31, 2023

    Arms and Interventions

    Arm Intervention/Treatment
    Retrospective Cohort of Aortic Coarctation

    Patients diagnosed as aortic coarctation and undergone corrected procedures from 2002 to Feb 28th 2019 were recruited in Beijing Anzhen Hospital, recording the results of clinical lab and echocardiography.

    Perspective Cohort of Aortic Coarctation

    Patients diagnosed as aortic coarctation and undergone corrected procedures after Mar. 1st 2019 will be recruited in Beijing Anzhen Hospital, recording the results of clinical lab and echocardiography.

    Outcome Measures

    Primary Outcome Measures

    1. Change in left ventricular mass [Prior to primary treatment and during follow-up visit(one month to 20 years for retrospective cohort and one year for prospective cohort)]

      Left ventricular mass will be measured by 2D echocardiography. For the retrospective cohort, the data is collected from the cases' medical record, and during follow-up visit.

    2. Hypertension [one month to 20 years after primary treatment for retrospective cohort and one year after primary treatment for prospective cohort]

      Both resting blood pressure and exercise-related blood pressure will be assessed for patients above 5 years old during the follow-up visit.

    Secondary Outcome Measures

    1. Left ventricular systolic function [one month to 20 years after primary treatment for retrospective cohort and one year after primary treatment for prospective cohort]

      Left ventricular systolic function assessed by echocardiography

    2. Left ventricular diastolic function [one month to 20 years after primary treatment for retrospective cohort and one year after primary treatment for prospective cohort]

      Left ventricular diastolic function assessed by echocardiography (TDI)

    3. Left ventricular systolic heart function of longitudinal myocardium [one month to 20 years after primary treatment for retrospective cohort and one year after primary treatment for prospective cohort]

      Left ventricular systolic heart function of longitudinal myocardium assessed by echocardiography (M mode Doppler).

    4. Exercise tolerance [one month to 20 years after primary treatment for retrospective cohort and one year after primary treatment for prospective cohort]

      Six minutes walking distance will be recorded and analyzed to evaluate the exercise tolerance. Echocardiographic images will be obtained after six minutes walking to assess the reserve function of left ventricle. Blood pressure will also be taken immediately after the Six minutes walking to analyze exercise-induced hypertension.

    5. Biomarkers of vascular inflammation [Prior to primary treatment and during follow-up visit(one month to 20 years for retrospective cohort and one year for prospective cohort)]

      Biomarkers of inflammation (hs-CRP). For the retrospective cohort, the data is collected from the cases' medical record, and during follow-up visit.

    6. Biomarkers of left ventricle remodeling [For the retrospective cohort, follow-up visit of 1 month to 20 years after primary treatment. For the prospective cohort, the data is collected prior to primary treatment and during follow-up visit of one year after primary treatment]

      Biomarkers of left ventricle remodeling (ST2)

    7. Biomarkers of left heart function [Prior to primary treatment and during follow-up visit(one month to 20 years for retrospective cohort and one year for prospective cohort)]

      Biomarkers of left heart function (BNP). For the retrospective cohort, the data is collected from the cases' medical record, and during follow-up visit.

    8. Biomarkers of hypertension phenotype related to aortic coarctation [one month to 20 years after primary treatment for retrospective cohort and one year after primary treatment for prospective cohort]

      Biomarkers of hypertension phenotype related to aortic coarctation

    9. Recoarctation [one month to 20 years after primary treatment for retrospective cohort and one year after primary treatment for prospective cohort]

      Recoarctation assessed by echocardiography or computed tomography angiography.

    10. All-cause death [20 years after primary treatment for retrospective cohort and one year after primary treatment for prospective cohort]

      The data is collected during follow-up visit at follow-up time point.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A to 17 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Diagnosis of isolated coarctation of the aorta, or accompanied with atrial septal defect(ASD), ventricular septal defect (VSD), patent ductus arteriosus( PDA), patent foramen ovale (PFO);

    • Patients who can cooperation with study procedures.

    Exclusion Criteria:
    • Co-morbidities that may independently affect cardiovascular function, including associated complicated congenital heart disease, such as hypoplastic left heart syndrome (HLHS), interruption of aortic arch (IAA), Shone Syndrome, moderate and severe mitral stenosis;

    • History of known vasculopathy, genetic syndromes, diabetes mellitus, hyperlipoidemia or other cardiovascular risk factors.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Beijing Anzhen Hospital Beijing Beijing China 100029

    Sponsors and Collaborators

    • Beijing Institute of Heart, Lung and Blood Vessel Diseases
    • Beijing Anzhen Hospital
    • Bayi Children's Hospital Affiliated to PLA Army General Hospital, China
    • Capital Institute of Pediatrics, China

    Investigators

    • Principal Investigator: Jie DU, PhD, Beijing Institute of Heart, Lung and Blood Vessel Diseases

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Beijing Institute of Heart, Lung and Blood Vessel Diseases
    ClinicalTrials.gov Identifier:
    NCT04011956
    Other Study ID Numbers:
    • PICC
    First Posted:
    Jul 9, 2019
    Last Update Posted:
    Jul 14, 2020
    Last Verified:
    Jul 1, 2020
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 14, 2020