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Treatment of cauda equina injury by autologous bone marrow mononuclear cells: a series of n of 1 trial

Treatment of cauda equina injury by autologous bone marrow mononuclear cells: a series of n of 1 trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000038220
Enrollment
Unknown
Registered
2020-09-14
Start date
2020-09-13
Completion date
Unknown
Last updated
2020-11-30

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

Conditions

Cauda equina injury

Interventions

The test cycle:autologous bone marrow mononuclear cells
Controlled cycle:Conventional treatment

Sponsors

Xiangyang No.1 People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) The diagnostic is cauda equina injury; (2) Older than 18 years, less than 75 years; (3) The cause of cauda equina injury has been removed and the disease is in a stable period; (4) The type of cauda equina injury was incomplete or the cauda equina was dividing but had been sutured; (5) Good compliance, willing to cooperate with the study, and patients signed informed consent

Exclusion criteria

Exclusion criteria: (1) The menstrual period was 3 days before surgery for female patients; (2) The puncture site has the possibility of infection or poor skin conditions; (3) Patients with associated malignant tumors; (4) Any disease known to seriously affect the immune system, or advanced blood system, etc.; (6) Women who are pregnant or breastfeeding, or who plan to become pregnant during the study period; (5) People are inability to communicate properly and incapacitation,or psychiatric conditions that may affect programme compliance,or at risk of suicide, or with a history of alcohol or illicit drug abuse; (6) People have participated in or are participating in other clinical trials within 3 months before enrollment; (7) The researcher does not consider it appropriate to participate in this study.

Design outcomes

Primary

MeasureTime frame
ASIA2000??;

Secondary

MeasureTime frame
Bladder residual urine measurement;VAS;Barthel ADL;Functional Independence Measure, FIM;Safety outcome indicator;

Countries

China

Contacts

Public ContactBin Pei

Xiangyang No.1 People's Hospital

xyxzyxzx@163.com+86 18995678520

Outcome results

None listed

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