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Safety and efficacy study of umbilical cord mesenchymal stem cells transplantation for the treatment of cerebral infarction

Safety and efficacy study of umbilical cord mesenchymal stem cells transplantation for the treatment of cerebral infarction

Status
Active, not recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONRC-12002929
Enrollment
Unknown
Registered
2012-12-05
Start date
2009-09-27
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cerebral infarction

Interventions

Lumbar puncture stem cells therapy:Infusion of umbilical cord mesenchymal stem cells
Control:Using conventional drug therapy, including the application of cerebral protection agent (such as cell two choline and intravenous infusion of 10 d/course), improve microcirculation (Salvia mil
Vein group:Infusion of umbilical cord mesenchymal stem cells

Sponsors

The 105th Hospital of PLA
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Individuals aged 18–80 years of both sexes were eligible for the study if they had the following characteristics: 1. Ischemic stroke in the middle cerebral artery (MCA) territory evidenced by computed tomography or MRI occurring within 14 days; 2. Recanalization of the involved MCA as assessed by transcranial Doppler studies or by magnetic resonance angiography; 3. A score between four and 17 according to the National Institutes of Health Stroke Scale (NIHSS).

Exclusion criteria

Exclusion criteria: 1. Ipsilateral carotid stenosis (>50%,by Doppler studies); 2. Neurological worsening (>four points in the NIHSS) before injection due to either edema or intracerebral hemorrhage; 3. Thrombophilias or primary hematological diseases; 4. Previous stroke with modifed Rankin Scale(mRS) of more than 2; 5. Neurodegenerative disorders; 6. Autoimmune disorders; 7. Intracardiac thrombus; 8. Sepsis; 9. History of neoplasia or other comorbidity that could impact a patients short-term survival; 10. renal failure (serum creatinine >2 mg/ml); 11. Pregnancy or previous participation in other clinical trials; 12. Diffculty in obtaining vascular access for percutaneous procedure; 13. Liver failure;(14)Lacunar stroke;(15)Any condition that in the judgment of the investigator would place the patient under undue risk.

Design outcomes

Primary

MeasureTime frame
NIHSS-Score;

Countries

China

Contacts

Public ContactQingsong Wang
wangqs65@yahoo.com+86 18909696277

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026