Last reviewed · How we verify
NCT04013646
Combination Therapy of Umbilical Cord Blood and Erythropoietin for Stroke Paients
Phase 1, PHASE2 trial testing Umbilical cord blood infusion in Stroke in 24 participants. Status unknown.
2 November 2020
Quick facts
| Lead sponsor | Bundang CHA Hospital |
|---|---|
| Phase | Phase 1, PHASE2 |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | quadruple |
| Primary purpose | treatment |
| Enrollment | 24 |
| Start date | 2 May 2019 |
| Primary completion | 2 November 2020 |
| Estimated completion | 2 November 2021 |
| Sites | 1 location across South Korea |
Drugs / interventions tested
- Umbilical cord blood infusion — full drug profile →
- Erythropoietin injection
- Placebo umbilical cord blood infusion
- Placebo erythropoietin injection
- Active rehabilitation
Conditions studied
- Stroke — all drugs for Stroke →
- Umbilical Cord Blood — all drugs for Umbilical Cord Blood →
- Erythropoietin — all drugs for Erythropoietin →
- Safety — all drugs for Safety →
Sponsor
Bundang CHA Hospital
Who can join
20 and older, any sex, with Stroke or Umbilical Cord Blood. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This clinical trial is a clinical trial for the evaluation of the safety and efficacy of umbilical cord blood (UCB) therapy, UCB and erythropoietin (EPO) combination therapy in adult stroke patients.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
Mechanism of inflammatory response and therapeutic effects of stem cells in ischemic stroke: current evidence and future perspectives.
Wang Y, Yuan T, Lyu T, Zhang L, et al · · 2025 · cited 16× · PMID 38767477 · DOI 10.4103/1673-5374.393104 -
Safety and efficacy of allogeneic umbilical cord blood cells and erythropoietin combination therapy in patients with subacute stroke.
Kim JM, Shin S, Lee D, Choi JI, et al · · 2025 · PMID 41456040 · DOI 10.1186/s13287-025-04856-8
Verify or expand the search:
- PubMed search for NCT04013646
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Currently open trials in the same condition.
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Other Bundang CHA Hospital trials
Trials by the same sponsor.
- NCT07366554 — Epigenetic Factors of Colorectal Adenoma in Korean · not yet recruiting
- NCT06982573 — The Effect of Magnetic Stimulation on Low Back Pain Relief and Muscle Mass Maintenance in Patients With ESRD · NA · recruiting
- NCT06982586 — A Prospective, Single-Center, Single-Arm, Investigator-Initiated Exploratory Clinical Trial to Assess the Safety of Repe · NA · not yet recruiting
- NCT06995274 — Umbilical Cord Blood Therapy in a Child With Eosinophilic Duodenitis and Autism Spectrum Disorder: a Case Study · NA · not yet recruiting
- NCT06543797 — A Pilot Clinical Trial Study to Determine the Safety of the Application of a Wearable Medical Electromagnetic Generator · EARLY_PHASE1 · not yet recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04013646 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 9 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Bundang CHA Hospital
- Last refreshed: 5 November 2020
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04013646.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing