From: In vivo experience with natural scaffolds for myocardial infarction: the times they are a-changin’
Scaffold material | Study name | Cell lines and/or other components | State | Follow-up | Main results/objectives | References/clinical trial identifier |
---|---|---|---|---|---|---|
Collagen | MAGNUM | Human mononuclear bone marrow stem cells | Completed with 20 patients | 10Â months | No adverse related events, 1 point reduction of New York Heart Association functional class, 26Â % reduction of LV end-diastolic volume, 22Â % improvement of LV filling deceleration time, 50Â % increase of scar thickness, 26Â % enhancement of EF | |
Fibrin | ESCORT | hESC | Recruiting patients | – | Study the number and nature of adverse events (clinical/biological abnormalities, arrhythmias and cardiac or extracardiac tumors). Test feasibility and efficacy of the scaffold in cardiac function recovery | NCT02057900 |
Alginate | AUGMENT-HF | – | Completed with 6 patients | 3 months | Increase of Kansas City Cardiomyopathy Questionnaire from 39.4 to 74, number of patients with New York Heart Association class III/IV reduced from 6 to 1. No improves in EF and LV end-diastolic and end-systolic volumes | [111] |
Gelatin | ALCADIA | Human cardiac-derived stem cells+bFGF | Completed with 6 patients | 6Â months | 12Â % increase in LV EF, 3.3Â % decrease of infarct size, maximal aerobic exercise capacity enhanced by 4.5Â ml/kg/min | [145], NCT00981006 |
SIS | – | – | Enrolling participants (by invitation only) | – | Evaluate scaffold safety and beneficial effects in heart function | NCT02139189 |