ClinicalTrials.Veeva

Menu

Human Umbilical Cord Mesenchymal Stem Cell in Cerebral Hemorrhage Sequela

S

Shenzhen Hornetcorn Biotechnology

Status and phase

Unknown
Phase 1

Conditions

Cerebral Hemorrhage

Treatments

Biological: Human umbilical cord mesenchymal stem cells

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT02283879
HYK-Cerebral hemorrhage

Details and patient eligibility

About

The purpose of this study is to evaluate the safety and efficacy of human umbilical cord mesenchymal stem cell(hUC-MSC) for cerebral hemorrhage sequela.

Full description

Human umbilical cord mesenchymal stem cells exhibit the potential to differentiate into neural cells, which have been confirmed in in vivo and in vitro experiments. There have been few clinical reports describing umbilical cord mesenchymal stem cells for treatment of cerebral hemorrhage.

To investigate the effects of hUC-MSC treatment for cerebral hemorrhage sequela, 20 patients with cerebral hemorrhage will be enrolled and receive 4 times of hUC-MSC transplantation.

Enrollment

20 estimated patients

Sex

All

Ages

40 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged 40-70 intracerebral hemorrhage patient
  • With stroke history of more than 3 months, less than 60 months
  • National Institutes of Health stroke scale(NIHSS) score of 7 or more points
  • Patient is stable (normal respiration, afebrile, BP less than mean arterial pressure of 125 mm of Hg, fasting blood sugar <7 mg, and normal urea/electrolytes for at least 48 hours.)

Exclusion criteria

  • History of neurological disease, head injury or psychiatric disorder;
  • Pregnant women;
  • Impaired liver function, abnormal blood coagulation, AIDS, HIV, combine other tumor or special condition;
  • Progressive apoplexy;
  • With malignant tumors.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

hUC-MSC treatment
Experimental group
Description:
Patients will receive human umbilical cord mesenchymal stem cells transplantation with a 12 months follow-up.
Treatment:
Biological: Human umbilical cord mesenchymal stem cells

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems