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Status unknownNCT03150342Updated May 16, 2017

Presentations of Hypertrophic Cardiomyopathy on Myocardial Perfusion Imaging

An observational study in Hypertrophic Cardiomyopathy and Myocardial Perfusion Imaging, sponsored by Far Eastern Memorial Hospital. Status unknown at 1 site in Taiwan. Open to participants aged 20 Years and older. Per ClinicalTrials.gov, last updated 2017-05-16.

Sponsored by Far Eastern Memorial Hospital · Observational

The sponsor has not verified this record recently (last verified May 2017), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-only
Time perspective
Retrospective
Enrollment
100
Ages
20 Years and older
Sex
All
01

Study summary

Chest pain and myocardial ischemia are prevailing features in patients with hypertrophic cardiomyopathy (HCM). Recently introduced single-photon emission computed tomography (SPECT) cameras with solid-state cadmium-zinc-telluride (CZT) detectors have been shown to decrease imaging time and improved the imaging quality of gated myocardial perfusion imaging (MPI). The investigators also correlate the MPI parameters with echocardiographic parameters. This study is to examine the spatial distribution of stress perfusion abnormalities and tissue injury in patients with HCM using a CZT SPECT camera.

Read the detailed description

The investigators will retrospectively evaluate myocardial perfusion patterns and cardiac function with Thallium (Tl)-201 gated dipyridamole MPI in patients with clinical diagnosis of HCM and patent coronary angiography between January 2013 and October 2016. The inclusion criteria included a spade-like configuration on left ventriculogram, or echocardiographic findings suggestive of HCM. The participants will be then divided into the following three groups: apical, concentric and septal forms. Regional perfusion would be analyzed using a 17-segment model from 0-4 degree (0=normal, to 4=absent perfusion); and summed stress score (SSS), summed rest score (SRS) and summed difference score (SDS) were calculated. Gated SPECT would be processed by quantitative gated SPECT (QGS) software (Cedars-Sinai Medical Center, Los Angeles, CA, USA) and ejection fraction phase analysis. Diastolic parameters would be also acquired by Doppler echocardiography, and correlated with MPI parameters.

02

Conditions studied

  • Hypertrophic Cardiomyopathy
  • Myocardial Perfusion Imaging

Keywords

  • CZT scanner
  • myocardial perfusion imaging
  • Hypertrophic Cardiomyopathy
03

In context

Cardiomyopathies

1,176 studies on the registry are indexed under Cardiomyopathies; 287 are open to participants now.

This study's planned enrollment of 100 is below the median of 153 across 515 observational studies indexed under Cardiomyopathies.

Browse Cardiomyopathies studies →

Lead sponsor

Far Eastern Memorial Hospital is the lead sponsor of 253 studies on the registry; 38 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

HCM patients with patent coronary artery who underwent MPI

Inclusion criteria

  • clinical diagnosis of HCM and patent coronary angiography between January 2013 and October 2016.

Exclusion criteria

Exclusion Criteria:

  • patient with prior myocardial ischemia, conduction abnormality, valvular disease or other cardiomyopathy
05

Study design

Observational model
Case-only
Time perspective
Retrospective
Enrollment
100 participants (estimated)
Patient registry
No

Interventions

  • Diagnostic testmyocardial perfusion imaging

    dipyridamole-stressed MPI scan using thallium-201

06

What researchers measure

Primary outcomes

  1. MPI results

    including perfusion abnormalities, and ejection fraction phase analysis results

    Time frame: January 2013 and October 2016.

07

Study locations

1 of 1 sites recruiting
  • Far Eastern Memorial Hospital
    New Taipei City, 220, Taiwan
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 16, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03150342
Lead sponsor
Far Eastern Memorial Hospital
Responsible party
Szu-Ying Tsai (Resident Physician, department of nuclear medicine, Far Eastern Memorial Hospital) — Principal investigator
First posted
May 12, 2017
Start date
May 8, 2017
Primary completion
Aug 31, 2017 (estimated)
Completion
Jun 30, 2018 (estimated)
Last update
May 16, 2017

Study contacts

Szu-Ying Tsai, MD
Contact
dorissyt@mail.femh.org.tw
+886289227000 ext. 1223
Yen-Wen Wu, MD, PhD
study director · Far Eastern Memorial Hospital

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in May 2017. You cannot join it, but the record below documents what was studied.

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