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Efficacy and safety of local stem cell transplantation for sequelae of spinal cord injury

Efficacy and safety of local stem cell transplantation for sequelae of spinal cord injury

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TNRC-12002477
Enrollment
Unknown
Registered
2014-09-21
Start date
2011-02-01
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

Spinal Cord Injury

Interventions

B:local stem cell transplantation by CT-guided punct

Sponsors

General Hospital of Chinese people's Armed Police Forces
Lead Sponsor

Eligibility

Sex/Gender
All
Age
24 Years to 52 Years

Inclusion criteria

Inclusion criteria: Clear diagnosis of spinal cord injury and the duration of patients is more than one year.

Exclusion criteria

Exclusion criteria: For Group A patients, the exclusion criteria included the following: (1) inflammation or skin ulceration at the surgical site; (2) patients with a bleeding tendency or coagulation defects; (3) patients in poor general condition who could not tolerate surgery and (4) patients with systemic organ dysfunction who could not tolerate surgery. To minimize the influence of other factors that could also affect neurological rehabilitation during the assessment of the efficacy of SC transplantation, the following circumstances were also excluded from Group A: (1) patients with incomplete SCI; (2) patients who still showed recovery trends in terms of nerve function; (3) patients with adhesions at the injury site that required surgical intervention; (4) patients with significant compressive lesions at the injury site that required surgical intervention; (5) patients with progressive loss of nerve function for unknown reasons; (6) patients with associated syringomyelia who required surgical intervention and (7) patients with associated spinal cord or epidural vascular malformations that required surgical intervention. For Group B patients, the exclusion criteria included the following: (1) patients with incomplete spinal cord injuries; (2) patients who still showed recovery trends in terms of nerve function; (3) patients with adhesions at the injury site that required surgical intervention; (4) patients with significant compressive lesions at the injury site that required surgical intervention; (5) patients with progressive loss of nerve function for unknown reasons; (6) patients with associated syringomyelia that required surgical intervention; (7) patients with associated spinal cord or epidural vascular malformations that required surgical intervention and (8) patients who could not be in the prone position or who could not remain in the prone position for more than 30 minutes.

Design outcomes

Primary

MeasureTime frame
AIS grading scale;ASIA score;

Countries

China

Contacts

Public ContactYihua An
riveran@163.com+86 10-57976848

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 21, 2026