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Study identifier: NCT06705023 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study to Assess Safety and Efficacy of Treating Symptomatic, Ischemic, Chronic Congestive Heart Failure Patients with an LVEF of ≤40% with Fresh, Uncultured, Autologous, Adipose-derived Regenerative Cells Isolated from Lipoaspirate.

Condition: Myocardial Injury · LV Dysfunction · Coronary Artery Disease  ·  Sponsor: Ralf Rothoerl

PhasePhase 2
Planned participants36
Who can joinAll sexes, 21 Years to 80 Years
Healthy volunteersNo

About this study

To investigate patients suffering from iHF and a LVEF of equal or less than 40% despite best medical treatment safety and efficacy of a single retrograde intra-cardiac venous (i.cv.) injection of UA-ADRCs isolated from lipoaspirate at the point of care, using the Transpose® RT / Matrase System (InGeneron, Houston, TX, USA) through an over-the- wire, small balloon catheter, advanced through the coronary si-nus and located within a coronary vein at the site of inter-est, versus patients on best medical treatment.

This description comes directly from the study's public registry record.

Talk to the study team

Anastassiya Ganina-Smelova, PhD  ·  +77024346421  ·  anastassiya_smelova@mail.ru

Aizhan Akhaeva, PhD  ·  +77075008522  ·  akhaeva@mail.ru

Always discuss trial participation with your own doctor first.

Locations (1)

National Scientific Medical CenterAstana, KazakhstanRecruiting

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Source record: clinicaltrials.gov/study/NCT06705023