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Not yet taking people in ChinaPhase 2

Tests umbilical cord stem cells for stroke recovery

Tests umbilical cord stem cells against placebo in adults with ischemic stroke.

Plain-language title generated from the registry record
Registry title: Clinical Trial of Umbilical Cord Mesenchymal Stem Cells in Subacute Ischemic Stroke

Key facts

Where
Beijing, ChinaSee the site
Phase
Phase 2

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 70 years old?

Source: NCT07197606, who can take part

Where in China

  • Xuanwu Hospital, Capital Medical UniversityBeijing, ChinaNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Shanghai IxCell Biotechnology Co., LTD
Trial code
NCT07197606
Record updated
29 September 2025
Original description
The goal of this clinical trial is to evaluate the efficacy, safety, and pharmacodynamic characteristics of Human Umbilical Cord Mesenchymal Stem Cells (hUC-MSCs) in adults with ischemic stroke in the anterior circulation during the recovery phase. Researchers will compare hUC-MSCs to a placebo to determine whether hUC-MSCs treatment is effective in treating recovery-phase anterior circulation ischemic stroke.Read full original descriptionShow less

A Multicenter, Double-Blind, Randomized, Placebo-Controlled, Phase II Clinical Study to Evaluate the Efficacy and Safety of IxCell hUC-MSC-S in Patients With Ischemic Stroke in the Recovery Phase

The goal of this clinical trial is to evaluate the efficacy, safety, and pharmacodynamic characteristics of Human Umbilical Cord Mesenchymal Stem Cells (hUC-MSCs) in adults with ischemic stroke in the anterior circulation during the recovery phase. Researchers will compare hUC-MSCs to a placebo to determine whether hUC-MSCs treatment is effective in treating recovery-phase anterior circulation ischemic stroke.

Inclusion: Age ≥18 years and ≤70 years, regardless of gender; 14 to 90 days after ischemic stroke; Clinical diagnosis of anterior circulation ischemic stroke; National Institutes of Health Stroke Scale (NIHSS) score is 6-20 points (inclusive), with NIHSS motor arm (item 5) or motor leg (item 6) score of 2-4 points, and NIHSS level of consciousness item (1a) score <2 points; It was anticipated that participants would either be able to give informed consent or have a legal representative who could do so.

Exclusion: People who had a history of epilepsy, dementia, Parkinson's disease, severe depression, or other neurological or psychiatric disorders; Intracranial hemorrhagic conditions; Pre-stroke mRS score >1; Severe cardiovascular disease; Severe pulmonary diseases.

ClinicalTrials.gov NCT07197606