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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01105520
Other study ID # ZU-XYZ-003
Secondary ID
Status Recruiting
Phase Phase 1
First received April 15, 2010
Last updated April 15, 2010
Start date January 2010
Est. completion date December 2015

Study information

Verified date April 2010
Source University of Zurich
Contact 01 Studienregister MasterAdmins
Phone +41 (0)44 255 11 11
Is FDA regulated No
Health authority Switzerland: Swissmedic
Study type Observational

Clinical Trial Summary

Patients included in the study are treated at the Klinik für Neurochirurgie USZ. The clinical course is documented at Paraplegikerzentrum Balgrist using validated diagnostic procedures (e.g. SCIM, ASIA, neurophysiology).

Study aims:

Prognostic value of clinical diagnosis and additional diagnostic procedures? Which parameters exhibit optimal prognostic power? Differences between tumor/AVM associated lesions and traumatic lesions? What can we learn for pathophysiology and treatment?

- Trial with surgical intervention


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 2015
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion criteria:

- Benign intraspinal process (tumor or vascular malformation AVM)

- Primary lesion caudal of the brainstem, affecting C1

- Cognitive ability to give written informed consent

Exclusion criteria:

- Metastases, malign tumors

- Traumatic lesions

- Myelitis, polyneuropathy

- Disc prolaps

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Procedure:
Diagnostic
SCIM Spinal Cord Independence Measure ASIA scale American Spinal Injury Association

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

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