Cardiac Sarcoidosis Multi-Center Prospective Cohort

Last updated: May 7, 2024
Sponsor: Ottawa Heart Institute Research Corporation
Overall Status: Active - Recruiting

Phase

N/A

Condition

Sarcoidosis

Treatment

N/A

Clinical Study ID

NCT01477359
UOHI-04
  • Ages 18-99
  • All Genders

Study Summary

Recent data has shown that sarcoidosis, presenting initially with cardiac manifestations (CS) of either conduction system disease or cardiomyopathy and sustained VT, is not uncommon. A Canadian physician survey found that most physicians do not investigate for CS as a possibility in these situations. Thus many patients with clinically important CS are going un-diagnosed. A study from Finland showed that missing the diagnosis of CS in these patients' leads to significant mortality and morbidity.

There are no published clinical consensus guidelines on treatment of CS. Corticosteroid therapy is advocated by most experts. This is based on very modest data from small retrospective observational studies using variable definitions of clinical response. The effect of corticosteroid treatment on the clinical course of CS has not been studied in prospective studies and will be one of the aims of this project. Recent physician surveys regarding CS, in Canada and the US, found that current clinical practice varies widely. The 2008 American College of Cardiology/American Heart Association/Heart Rhythm society guidelines recommend implantation of a defibrillator (Class IIa recommendation) to prevent sudden cardiac death. The most recent Canadian device therapy guidelines do not mention CS.

A multi-center collaborative approach to study CS is greatly needed." The investigators propose exactly that i.e. a multi-center prospective cohort to start to answer clinical questions. The investigators have formed the CANADIAN CARDIAC SARCOIDOSIS RESEARCH GROUP. The group includes respirologists with an interest in sarcoidosis, cardiac electrophysiologists, cardiac imaging specialists with extensive experience in imaging of sarcoidosis and biostatisticians. The research will be in two phases; a registry of current diagnostic approaches, treatment and prognosis, and a randomized clinical trial of the effect of corticosteroid treatment on the clinical course of cardiac sarcoidosis.

Eligibility Criteria

Inclusion

Inclusion Criteria: To diagnose Clinically Manifest CS all following criteria must be met:

(i) Positive biopsy* for Sarcoid (either EMB or extra-cardiac) AND/OR (ii) CT Chest highlysuggestive of pulmonary sarcoidosis AND (iii) one or more of the following clinicalfeatures:

  • advanced conduction system disease (sustained Mobitz II AV block or third degree AVblock)
  • non- sustained or sustained ventricular arrhythmia
  • ventricular dysfunction (LVEF < 50% and/or RVEF < 40%) AND (iv) No alternativeexplanation for clinical features AND (v) FDG-PET suggestive of active CS To diagnose clinically silent CS all of the following criteria must be met

(i) Biopsy proven extra-cardiac sarcoidosis AND/OR (ii) CT Chest highly suggestive of pulmonary sarcoidosis AND (iii) CMR suggestive of cardiac sarcoidosis AND (iv) Does not have criteria for clinically manifest CS ie. should not have any offollowing

  • advanced conduction system disease (sustained Mobitz II AV block or third degree AVblock)
  • non- sustained or sustained ventricular arrhythmia
  • ventricular dysfunction (LVEF < 50% and/or RVEF < 40%) Patients with negative CMR will be designated as 'extra-cardiac sarcoidosis with noevidence of CS' and followed as control

Exclusion

Exclusion Criteria:

  • unable or unwilling to provide informed consent
  • patients who are pregnant or lactating
  • patients with known claustrophobia
  • age < 18 years

Study Design

Total Participants: 1500
Study Start date:
August 01, 2012
Estimated Completion Date:
December 31, 2025

Study Description

Baseline assessment of Clinically Manifest CS patients consists of: history, echocardiogram, ECG, chest CT scan, FDG-PET scan, blood for biomarkers within 2 months of the PET scan, cardiac MRI and possibly a signal average ECG and biopsy (encouraged-either endomyocardial or extra-cardiac).

Follow-up and clinical management of clinically manifest patients diagnosed with CS will occur at 3-6 months with a repeat FDG-PET scan and blood biomarkers. Follow-up will then be annually with an echo and ECG. Treatment with steroids/immunosuppressants and device therapy will be at the discretion of the treating physician.

Baseline assessment of patients diagnosed with extra-cardiac sarcoidosis and being screened for CS consists of: history, echocardiogram, ECG, holter, chest CT scan, biopsy, and cardiac MRI (CMR). If the CMR is suggestive of CS the patient will be have a FDG-PET scan done and be followed as a Clinically Silent patient. They will be contacted every 2 years. If the CMR is negative the patient will be followed as a extra-cardiac sarcoidosis patient with no evidence of CS and be in the control group. They will be contacted at 5 years and at the time of study completion.

All patients will be followed until the last patient recruited has been followed for 4 years.

The occurrence of the primary and secondary outcomes will be assessed in treated and untreated patients.

There will be 2 imaging core labs. The PET core lab will be located at UOHI under the direction of Dr. Robert Beanlands. The CMR core lab will be under the direction of Dr. Mathias Friedrich (McGill University). All scans will be read in the core labs by physicians who are blinded to the clinical details of the patients.

The Biomarker core lab will be at The University of Ottawa Heart Institute under the leadership of Dr P Liu.

Connect with a study center

  • Libin Cardiovascular Institute of Alberta

    Calgary, Alberta T2N 2T9
    Canada

    Active - Recruiting

  • University of Alberta Hospital

    Edmonton, Alberta T6G 2B7
    Canada

    Active - Recruiting

  • St. Paul's Hospital

    Vancouver, British Columbia V5Z 1M9
    Canada

    Active - Recruiting

  • Victoria Cardiac Arrhythmia Trials Inc.

    Victoria, British Columbia V8R 4R2
    Canada

    Site Not Available

  • St. Boniface General Hospital

    Winnipeg, Manitoba R2H 2A6
    Canada

    Site Not Available

  • Saint John Regional Hospital, NB Heart Centre

    Saint John, New Brunswick E2L 4L2
    Canada

    Site Not Available

  • St. John's Health Sciences Centre

    St. John's, Newfoundland and Labrador A1B 3V6
    Canada

    Site Not Available

  • QEII Health Sciences Center

    Halifax, Nova Scotia B3H 3A7
    Canada

    Active - Recruiting

  • Hamilton Health Sciences Centre

    Hamilton, Ontario L8L 2X2
    Canada

    Active - Recruiting

  • Kingston General Hospital

    Kingston, Ontario K7L 2V7
    Canada

    Site Not Available

  • London Health Sciences Centre

    London, Ontario N6A 5A5
    Canada

    Active - Recruiting

  • Southlake Regional Health Centre

    Newmarket, Ontario L3Y 2P9
    Canada

    Active - Recruiting

  • University of Ottawa Heart Institute

    Ottawa, Ontario K1Y 4W7
    Canada

    Active - Recruiting

  • Toronto General Hospital

    Toronto, Ontario M5G 2C4
    Canada

    Active - Recruiting

  • Centre Hospitalier de l"Universite de Montreal-Hotel Dieu

    Montreal, Quebec H2W 1T8
    Canada

    Site Not Available

  • McGill University Health Centre

    Montreal, Quebec H3G 1A4
    Canada

    Active - Recruiting

  • Montreal Heart Institute

    Montreal, Quebec H1T 1C8
    Canada

    Active - Recruiting

  • Centre Hospitalier de L'Université de Sherbrooke

    Montréal, Quebec J1H 5N4
    Canada

    Site Not Available

  • Centre Hospitalier de L'Université de Sherbrooke

    Montréal, Quebec J1H 5N4
    Canada

    Site Not Available

  • Prairie Vascular Research Inc-Regina General Hospital

    Regina, Saskatchewan S4P 0W5
    Canada

    Active - Recruiting

  • Hokkaido University

    Sapporo, 060-8638
    Japan

    Active - Recruiting

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