Actively Recruiting
Subarachnoid-Subarachnoid (S-S) Bypass Versus Adhesion Lysis in Spinal Arachnoiditis and Syringomyelia
Led by Xuanwu Hospital, Beijing · Updated on 2024-04-19
200
Participants Needed
1
Research Sites
156 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To determine whether Subarachnoid-Subarachnoid (S-S) Bypass results in better patient outcomes with fewer complications and improved quality of life compared to intradural adhesion lysis in individuals with Spinal Arachnoiditis and Syringomyelia.
CONDITIONS
Official Title
Subarachnoid-Subarachnoid (S-S) Bypass Versus Adhesion Lysis in Spinal Arachnoiditis and Syringomyelia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- History of traumatic spinal cord injury or other infection
- Evidence of progressive neurological deficit and/or pain syndrome
- MRI showing syringomyelia due to spinal trauma or other infection
- Willingness to complete a minimum follow-up period of more than 1 year
You will not qualify if you...
- Chiari-malformation
- Myelomalacia
- Subarachnoid cyst
- Syringomyelia caused by other spinal diseases such as degenerative spinal disease
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Fengzeng Jian
Beijing, Beijing Municipality, China, 100053
Actively Recruiting
Research Team
F
fengzeng jian
CONTACT
Y
yuan chenghua
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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