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A Patient Registry at the Neurosurgery Department

This study is enrolling participants by invitation only.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01628406
First Posted: June 26, 2012
Last Update Posted: May 30, 2016
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
University of Zurich
  Purpose

The investigators record all indications, treatments and outcomes from patients treated at the Neurosurgery Department.

  • Trial with surgical intervention

Condition Intervention Phase
Patients Treated at the Neurosurgery Department Procedure: Treatment at the neurosurgery departement Phase 1

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Retrospective
Official Title: A Patient Registry at the Neurosurgery Department.

Further study details as provided by University of Zurich:

Primary Outcome Measures:
  • neurological outcome [ Time Frame: 1 year ]
    validated scales like KPSS or NIHSS

  • social outcome [ Time Frame: 1 year ]
    e.g. activity of daily living, employment status


Estimated Enrollment: 12000
Study Start Date: June 2012
Estimated Study Completion Date: August 2022
Estimated Primary Completion Date: August 2022 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Patients treated at the neurosurgery department
Patients treated at the neurosurgery department
Procedure: Treatment at the neurosurgery departement
Treatment at the neurosurgery departement

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
All patients treated at the Neurosurgery Department
Criteria

Inclusion criteria:

All patients treated at the Neurosurgery Department

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01628406


Locations
Switzerland
University Hospital Zurich, Neurosurgery
Zurich, ZH, Switzerland, 8091
Sponsors and Collaborators
University of Zurich
Investigators
Principal Investigator: Johannes Sarnthein, MD University Hospital Zurich, Division of Neurosurgery
  More Information

Responsible Party: University of Zurich
ClinicalTrials.gov Identifier: NCT01628406     History of Changes
Other Study ID Numbers: 122
First Submitted: June 21, 2012
First Posted: June 26, 2012
Last Update Posted: May 30, 2016
Last Verified: May 2016