Results of Tc99m-Maraciclatide Scintigraphy in Subjects With Diabetes Mellitus and Heart Failure With Preserved Left Ventricular Ejection Fraction
Stopped early · Phase 2
Conditions studied: Diabetes Mellitus, Heart Failure
In brief
The purpose of this study is to evaluate the results of 99mTc maraciclatide scintigraphy in diabetic subjects with HFPEF. A maximum of 20 subjects with Diabetes Mellitus (DM) and Heart Failure With Preserved Left Ventricular Ejection Fraction (HFPEF) will be enrolled and imaged with 99mTc maraciclatide. In addition, a maximum of 10 subjects with DM and diastolic dysfunction but no diagnosis of heart failure (HF) will be enrolled and imaged with 99mTc-maraciclatide.
Key facts
- Study ID
- NCT01440517
- Run by
- GE Healthcare
- People needed
- 4
- Starts
- 2011-08-01
- Expected to finish
- 2012-03-01
- Last updated by the study team
- 2014-02-04
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- The subject is between 18 and 80 years of age.
- The subject was diagnosed with DM type 2 based upon accepted clinical criteria and currently takes at least one diabetes medication.
- For HF subjects: The subject was diagnosed with HF with preserved EF within the previous 1 year, at which time LVEF was determined to be ≥45%.
- For comparison subjects: The subject was determined to have diastolic dysfunction on EKG within the previous year and currently has no signs or symptoms of HF.
- The subject has been clinically stable for at least 7 days prior to the study imaging procedures (e.g., not experiencing continuing chest pain, hemodynamic instability, worsening HF symptoms, or clinically significant arrhythmia).
You may not qualify if…
- The subject had an acute myocardial infarction within the past 30 days.
- The subject had a cardiac revascularization (e.g., percutaneous transluminal coronary angiography [PTCA], percutaneous coronary intervention (PCI), or coronary artery bypass graft [CABG]) within the past 30 days.
- The subject has severe renal dysfunction.
- The subject is claustrophobic or has a movement disorder that prevents him/her from lying still in a supine position for up to 20 minutes at a time.
- The subject has participated in a research study using ionizing radiation in the previous 12 months.
Where it is running
- GE Healthcare — Princeton, New Jersey, United States
Full record on ClinicalTrials.gov
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