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Clinical Trials/NCT01415024
NCT01415024
Unknown
Phase 4

Resynchronization in Paced Heart Failure Patients With ICD Indication

Schuechtermann-Klinik1 site in 1 country30 target enrollmentMay 2011

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Heart Failure
Sponsor
Schuechtermann-Klinik
Enrollment
30
Locations
1
Primary Endpoint
LV dp/dt pressure during dual LV CRT stimulation vs. conventional biventricular pacing
Last Updated
14 years ago

Overview

Brief Summary

Today patients with a Cardiac Resynchronization Therapy (CRT) indication usually receive 2 ventricular leads, right ventricular (RV) apex and left ventricular (LV) (postero-) lateral, gaining a responder rate of approximately 70%. However, the physiological agitation of the left ventricle takes place over two pathways. Therefore single point stimulation might be insufficient for a dilated, insufficiently and asynchronously contracting left ventricle, resulting in either insufficient or no response to the therapy.

In the "CRT ICD Dual LV" study the patients receive a second LV lead in an anterior vein. When this lead is placed, temporary dual LV stimulation is started. To assess the effectivity of the dual LV lead stimulation intraoperatively a LV dp/dt-pressure measurement is taken. If there is an increase in LV dp/dt, the patients will be stimulated with both leads permanently. If not they will be stimulated conventionally.

The patients participating in this study are monitored for 12 months after implantation.

Registry
clinicaltrials.gov
Start Date
May 2011
End Date
May 2012
Last Updated
14 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Schuechtermann-Klinik

Eligibility Criteria

Inclusion Criteria

  • EF less than 35 percent
  • CAD or dilatative Cardiomyopathy
  • Sinus rhythm
  • NYHA III or IV, stable recompensated
  • QRS more than 120ms
  • Patient signed Consent Form
  • Age more than 18 and less than 80 y

Exclusion Criteria

  • permanent atrial Fibrillation
  • permanent AV-Block II or III
  • Tricuspidal- and or artificial aortic valve
  • Indication for ACB or ACB less than 3 months ago
  • myocardial infarction less than 3 months
  • hypertrophic obstructive Cardiomyopathy; constrictive Pericarditis
  • heartfailure with iv catecholamine therapy
  • Manifested, uncontrolled, Hypo- oder Hyperthyreosis
  • Severe renal insufficiency with Creatinine more than 2,5 mg per dL
  • patients, who did not sign the consent form

Outcomes

Primary Outcomes

LV dp/dt pressure during dual LV CRT stimulation vs. conventional biventricular pacing

Time Frame: Implantation with pressure measurement will take place in the first week

Secondary Outcomes

  • Leftventricular endsystolic volume(12 month)

Study Sites (1)

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