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Subarachnoid-Subarachnoid (S-S) Bypass Versus Adhesion Lysis in Spinal Arachnoiditis and Syringomyelia

Syringomyelia Clinical Trial

Official title:
Subarachnoid-Subarachnoid (S-S) Bypass Versus Adhesion Lysis in Spinal Arachnoiditis and Syringomyelia

Clinical Trial Summary

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.

Clinical Trial Description

Participants with Spinal Arachnoiditis and Syringomyelia will be randomized to either have a Subarachnoid-Subarachnoid (S-S) Bypass or intradural adhesion Lysis. The participant will then return to the neurosurgeon's office at the following time points which are consistent with standard of care practice: 3-6 months, 12 and 24 months. At these visits, the clinician will complete a physical exam and the participant will report on the prognosis of symptoms and complete questionnaires. A spine MRI will be performed 3-6 months, 12 and 24 months after the decompression. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06375759
Study type Interventional
Source Xuanwu Hospital, Beijing
Contact fengzeng jian
Phone 01083198899
Email jianfengzeng@xwh.ccmu.edu.cn
Status Recruiting
Phase N/A
Start date April 2024
Completion date April 2027
View Details
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