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NCT03420833Completed

Metabolic Mapping and Cardiac Resynchronization

Metabolic Mapping and Cardiac Resynchronization (Aim 1)

Source: ClinicalTrials.gov · Last updated 23 Jan 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The purpose of this study is to gather information on the safety and effectiveness of cardiac resynchronization therapy (CRT) in patients who have mild heart failure (HF) and left bundle branch block (LBBB).

Status (registry)
Completed
Study type
Interventional
Enrollment
82 (actual)
First submitted
29 Jan 2018
Start date
20 Aug 2018
Primary completion date
19 Dec 2023
Lead sponsor
Yong-Mei Cha
NCT number
NCT03420833

What you commit to

  • Study type: Interventional
  • Participants enrolled: 82
  • From 20 Aug 2018 to the primary completion date, 19 Dec 2023
  • 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.

Prior treatment

  • Female patients who is pregnant or not on a reliable form of birth control. Women of childbearing potential are required to have negative pregnancy test within the 7 days prior to device implant

Other illness

  • Advanced comorbid conditions with life expectancy \<1 year

Age

  • Patient is \<18 of years of age

Other

  • Patient has a CRT device
  • Unwilling or unable to return for required follow-up visits
  • Patient decides study participation is cost-prohibited

Who the study is looking for

  • Left Ventricular Ejection Fraction (LVEF) 35%-50%
  • New York Heart Association (NYHA) class I-II
  • QRS duration of ≥120ms
  • Left bundle branch block (LBBB)
  • Patient is able to receive a transvenous pectoral CRT implant
  • Patient is able to sign informed consent
  • Two echocardiograms are required to confirm a stable reduced LVEF
  • Patient is on optimal and stable medical therapy (ACE inhibitor or angiotensin II type 1 (AT1 )blocker, beta blocker, etc. over the last 6 months)

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
Mayo Clinic in Rochester
Coordinator of this site? Confirm its status
RochesterUnited StatesUnknown status

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