Skip to content

Targeted left ventricular lead placement in cardiac resynchronisation therapy

TARgeted left ventricular lead placement to Guide cardiac rEsynchronisation Therapy in patients with heart failure: a randomised prospective study (TARGET Study)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN19717943
Enrollment
220
Registered
2011-02-08
Start date
2009-04-01
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascualr disease/heart failure/device therapy Circulatory System Heart failure

Interventions

All patients schedules for CRT who are suitable candidates are randomised into one of two groups. All patients have baseline tests to include echocardiography, NYHA class assessment, 6-minute walk tes

Sponsors

Papworth Hospital NHS Foundation Trust (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients (aged 18 years or older, either sex) limited by symptoms of heart failure (New York Heart Association Class III - IV) 2. Left ventricular ejection fraction (LVEF) of less than or equal to 35% and QRS width of greater than or equal to 120 ms despite maximally tolerated doses of standard heart failure treatment (diuretics, angiotensin converting enzyme (ACE) inhibitors, angiotensin receptor blockers, beta blockers and aldosterone antagonists)

Exclusion criteria

Exclusion criteria: 1. Limiting angina 2. Myocardial infarction within preceding 3 months 3. Significant LV hypertrophy 4. Severe co-morbid illness

Design outcomes

Primary

MeasureTime frame
Response to treatment defined as greater than 15% reduction in Left Ventricular End Systolic Volume at 6 months follow up

Secondary

MeasureTime frame
Clinical Improvement in combined endpoint of 6 minute walk test performance, Minnesota Living with Heart Failure Questionnaire and NYHA Class

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 26, 2026