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Simple foramen magnum decompression with foramen magnum decompression for the treatment of syringomyelia shunt Arnold - Chiari malformation type I merger syringomyelia safety and effectiveness analysis

Simple foramen magnum decompression with foramen magnum decompression for the treatment of syringomyelia shunt Arnold - Chiari malformation type I merge syringomyelia the safety and effectiveness analysis-a prospectie, non-randomized, controlled clinical trials

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONRC-13003609
Enrollment
Unknown
Registered
2013-05-09
Start date
2013-06-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Arnold-Chiari malformation with syringomyelia

Interventions

Experimental:foramen magnum decompression
B:foramen magnforamen magnum decompression + for the treatment of syringo-subarachnoid um decompression

Sponsors

The second affiliated hospital of Harbin medical university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) the clinical symptoms and imaging diagnosis of Arnold - Chiari malformation type I merge patients with syringomyelia; (2) aged > 18 years; (3) Arnold - Chiari malformation with syringomyelia patients, is not restricted to problems such as gender, race and region, but limit the specific operation method (foramen magnum or posterior fossa decompression, foramen magnum or posterior fossa decompression + syringomyelia bypass surgery); (4) voluntarily accept regular follow-up as required; (5) the patient and family to informed consent of the subjects.

Exclusion criteria

Exclusion criteria: (1) with other related diseases or complications, such as tumor, bone disease, infection, osteoporosis, spinal fractures and mental illness, etc.; (2) no intend to participate in any clinical trials or researchers.

Design outcomes

Primary

MeasureTime frame
Postoperative complications occurre;

Secondary

MeasureTime frame
Success rate of surgery;Postoperative recurrence rate;Postoperative sensory, motor, improve nerve dysfun;Improvement of postoperative pain;

Countries

China

Contacts

Public ContactSun Chongyi

The second affiliated hospital of Harbin medical university

spine1972@yahoo.com+86 15204600666

Outcome results

None listed

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