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A retrospective study of spontaneous cervical epidural hematoma patients

A retrospective study of spontaneous cervical epidural hematoma patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000041498
Enrollment
Unknown
Registered
2020-12-27
Start date
2020-12-21
Completion date
Unknown
Last updated
2021-03-15

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

Conditions

Spontaneous cervical spinal epidural hematoma

Interventions

The time points between onset and the surgery is less than 8 hours:Nil
The time points between onset and the surgery is between 8 hours and 24 hours:Nil
The time points between onset and the surgery is more than 24 hours:Nil

Sponsors

The People's Hospital of Guangxi Zhuang Autonomous Region
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with spontaneous cervical intraspinal epidural hematoma were diagnosed in our hospital from January 2006 to January 2019; 2. Patients were given stage I cervical spinal canal decompression and epidural hematoma removal and internal fixation after admission; 3. High compliance and complete follow-up were conducted after operation.

Exclusion criteria

Exclusion criteria: 1. Non-specific spinal infection; 2. Spinal tuberculosis; 3. Cervical spine tumor; 4. Cervical fracture and dislocation; 5. Cervical spine injury without fracture and dislocation; 6. History of previous cervical surgery; 7. Hemophilia.

Design outcomes

Primary

MeasureTime frame
ASIA score;JOA score;VAS score;

Countries

China

Contacts

Public ContactHaoxi Li

The People's Hospital of Guangxi Zhuang Autonomous Region

volvoxc-90@163.com+86 18677154868

Outcome results

None listed

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