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Therapeutic Areas: Oncology | Trauma/Emergency Medicine | Cardiology/Vascular Diseases
Disease Category: Surgery
Trial Information
Planning to get a CRT-D
Ask your doctor if you would be a good candidate for the RESPONSE-HF research study.
Purpose: To compare the pacing function of CRT-D devices with and without a slight delay timing feature in patients who are not responding appropriately to treatment from their CRT-D.
Target Candidates: Patients planning to get a CRT-D.
Inclusion Criteria:
- Standard indication for a CRT-D.
Exclusion Criteria:
- Heart surgery in previous 6 months.
- Pregnancy.
Details: During your standard device follow-up visits for the nine months following your procedure, research data will be collected. Research data includes such things as questionnaires, hall walk, and echocardiogram. If at your three-month visit you are not responding appropriately to your device, you will be randomized to a pacing group. If you are appropriately responding, you will be withdrawn from the study.
If interested - call Irene Glenn 243-0046 or page 6836
PI: Dr. John DiMarco; HRB-ISR #12424; Location - UVa Health System
www.healthsystem.virginia.edu/clinical_trials
Irene Harvey MS
University of Virginia
School of Medicine
Cardiovascular Medicine (Heart Center), Internal Medicine
Charlottesville, VA 22908
Phone: 434-243-0046
Fax: --
EMail: img4k@virginia.edu
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Research Center Information: University of Virginia
If you would like to learn more about participating in this study, please send an e-mail message using the form below.
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