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Clinical Trials/EUCTR2009-013112-12-GB
EUCTR2009-013112-12-GB
Active, not recruiting
Not Applicable

Randomised Controlled Trial To Compare The effects of G-CSF(Granocyte™) And Autologous Bone Marrow Progenitor Cells On Quality Of Life And Left Ventricular Function In Patients with Idiopathic Dilated Cardiomyopathy - REGENERATE-DCM

Barts & the London NHS Trust0 sitesMarch 17, 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Idiopathic Dilated Cardiomyopathy
Sponsor
Barts & the London NHS Trust
Status
Active, not recruiting
Last Updated
10 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 17, 2010
End Date
TBD
Last Updated
10 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 60 symptomatic patients with a confirmed diagnosis of dilated cardiomyopathy (NYHA II\-III) attending a ‘Heart Failure clinic’ who are on optimal heart failure treatment, with no further treatment options, under supervision from their physician or heart failure nurse specialist.
  • Patients who are NYHA II that have been hospitalised with a dilated cardiomyopathy related condition.
  • Prior to recruitment to the study patients at risk of ventricular arrhythmia will have undergone electrophysiological assessment and appropriate clinical management (including implantable defibrillator insertion) where indicated (as per NICE guidelines).
  • Coronary angiography will be performed where necessary to confirm the diagnosis and ensure no other conventional treatment options are indicated.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range
  • F.1\.3 Elderly (\>\=65 years) yes
  • F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • Patients who satisfy one or more of the following criteria are not suitable for inclusion in the study:
  • Documented ejection fraction \>45% (any imaging modality)
  • The presence of cardiogenic shock
  • The presence of acute left and/or right sided pump failure as judged by the presence of pulmonary oedema and/or new peripheral oedema
  • Known severe pre\-existent left ventricular dysfunction (ejection fraction \<10%) prior to randomisation
  • Congenital cardiac disease
  • Cardiomyopathy secondary to a reversible cause that has not been treated e.g. thyroid disease, alcohol abuse, hypophosphataemia, hypocalcaemia, cocaine abuse, selenium toxicity \& chronic uncontrolled tachycardia
  • Cardiomyopathy in association with a neuromuscular disorder e.g. Duchenne’s progressive muscular dystrophy
  • Previous cardiac surgery
  • Contra\-indication for bone marrow aspiration

Outcomes

Primary Outcomes

Not specified

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