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Clinical studies related to the use of cerebrospinal fluid drainage in patients with spinal cord injury

Clinical studies related to the use of cerebrospinal fluid drainage in patients with spinal cord injury

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400092804
Enrollment
Unknown
Registered
2024-11-24
Start date
2024-11-24
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

Spinal cord injury

Interventions

Case group:None

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: ? diagnosis of acute C4 - C8 spinal cord injury and visit within 24 hours of injury; ?Grade A, B, or C on the American Spinal Cord Injury Association (ASIA) Impairment Scale based on initial evaluation; ? 18 to 75 years of age; ? complete medical records, including detailed clinical data, laboratory results, imaging results, and follow-up records during the course of treatment.

Exclusion criteria

Exclusion criteria: 1. SCI due to penetrating injury. 2. Previous history of SCI. 3. Concomitant severe head injury (Glasgow Coma Scale < 14 with clinically significant abnormalities on head CT). 4. Presence of a pre-existing neurological or psychiatric disorder that would affect accurate assessment and follow-up. 5. Has a history of chemical dependence or significant psychosocial disorder (which may affect outcomes or participation) and has been < 1 year. 6. Females of childbearing potential with a positive serum ß - hCG pregnancy test or uterine urine pregnancy test. 7. Have acquired immunodeficiency syndrome or related syndromes. 8. Has an active malignancy or a history of aggressive malignancy within the past 5 years (excluding superficial basal cell carcinoma or squamous cell carcinoma of the skin that has been definitively treated).

Design outcomes

Primary

MeasureTime frame
Visual Analog Scale;Spinal perfusion pressure, SCPP;Changes of ASIA grade ;

Secondary

MeasureTime frame
Motor and sensory function;Anal sphincter function;

Countries

China

Contacts

Public ContactYuan Feng

Affiliated Hospital of Xuzhou Medical University

cnxzyf@163.com+86 159 0520 1635

Outcome results

None listed

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