Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
ID06375759

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

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating whether Subarachnoid-Subarachnoid (S-S) Bypass leads to better outcomes with fewer complications and improved quality of life compared to intradural adhesion lysis in people with Spinal Arachnoiditis and Syringomyelia. This study compares two surgical approaches to treat these conditions, focusing on patient recovery and symptom improvement over time. Participants will be randomly assigned to either receive the S-S Bypass or intradural adhesion lysis. The S-S Bypass involves placing silicone tubes between the normal subarachnoid spaces after careful dissection, while adhesion lysis involves microsurgical removal of scar tissue followed by dural repair. After surgery, participants will have follow-up visits at 3-6 months, 12 months, and 24 months. During these visits, doctors will conduct physical exams, assess symptoms, and collect questionnaire responses. Spine MRIs will be done at each follow-up to monitor changes. Researchers will track complications at 12 months and evaluate improvements in syrinx size, neurological function, and spinal condition scores over the 24-month period. This monitoring helps understand the safety and effectiveness of each surgical procedure.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

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 infection
  • Willingness to be followed for more than 1 year
Not Eligible

You will not qualify if you...

  • Presence of Chiari-malformation
  • Presence of myelomalacia
  • Presence of 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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery

Duration - Single surgical procedure

Participants undergo either Subarachnoid-Subarachnoid (S-S) Bypass or Intradural Adhesion Lysis as treatment for spinal arachnoiditis and syringomyelia.

1 visit (in-person)

Post-operative Follow-up

Duration - Up to 24 months

After surgery, participants return for follow-up visits where physical exams, symptom assessments, and questionnaires are completed. Spine MRIs are performed to monitor progress.

Visits at 3 to 6 months, 12 months, and 24 months (in-person)

Trial Site Locations

Total: 1 location

1

Fengzeng Jian

Beijing, Beijing Municipality, China, 100053

Actively Recruiting

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Research Team

F

fengzeng jian

Y

yuan chenghua

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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Frequently Asked Questions

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Published Research Related To This Trial

Intradural Pathology Causing Cerebrospinal Fluid Obstruction in Syringomyelia and Effectiveness of Foramen Magnum and Foramen of Magendie Dredging Treatment.

Jian Guan, Chenghua Yuan, Can Zhang...

https://pubmed.ncbi.nlm.nih.gov/32805463

Long-Term Impairment of the Blood-Spinal Cord Barrier in Patients With Post-Traumatic Syringomyelia and its Effect on Prognosis.

Chenghua Yuan, Pingchuan Xia, Wanru Duan...

https://pubmed.ncbi.nlm.nih.gov/38014747