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NCT02814942Recruiting

Prospective Evaluation of Asians With CRT for Heart Failure

Source: ClinicalTrials.gov · Last updated 9 Mar 2021 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Aim:To determine the baseline characteristics of heart failure patients in Singapore undergoing cardiac resynchronization therapy (CRT); the long term outcome and predictors of response to CRT. Methodology:Among patients undergoing CRT for severe heart failure according to indications stipulated in international Cardiology guidelines, baseline demographic data is collected. Age, gender, NYHA functional class, co-morbidities, QRS width on ECG, presence of left bundle branch block pattern on ECG, presence of atrial fibrillation, left ventricular ejection fraction (LVEF) on echocardiogram, ventricular dimensions, 6 min walk test distance are collected. In addition, during the CRT implant procedure, blood is drawn from the vascular access and analysed for NT-pro BNP levels and other biomarkers of heart failure. The echocardiographic and ECG parameters and blood biomarkers are reanalysed at 6 months and 12 months following CRT implant. Response to CRT is defined as a reduction in the iLVESV (left ventricular end-systolic volume index to body surface area) of \>/= 15% and/or an increase in the LVEF of \>/= 10%.

Status (registry)
Recruiting
Study type
Observational
Enrollment
500 (estimated)
First submitted
22 Jun 2016
Start date
Jan 2011
Primary completion date
Dec 2030
Lead sponsor
National University Heart Centre, Singapore
NCT number
NCT02814942

What you commit to

  • Study type: Observational
  • Planned participants: 500
  • From Jan 2011 to the primary completion date, Dec 2030
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Infection

Age

  • \< 18 years of age

Other

  • Pregnant
  • Unable to consent

Who the study is looking for

  • Broad QRS (\>120 ms)
  • EF \< 40%
  • Symptomatic heart failure
  • Not on optimal medical therapy

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
National University Hospital
Coordinator of this site? Confirm its status
SingaporeSingaporeRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.