Postencephalitic Symptoms After Tick Borne Encephalitis

NCT ID: NCT00941590

Last Updated: 2009-07-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-07-31

Brief Summary

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The purpose of this study is to assess clinical outcome in patients with tick borne encephalitis.

Detailed Description

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Conditions

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Central European Encephalitis

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients with tick borne encephalitis.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* serologically proved tick borne encephalitis in patients \> 15 years

Exclusion Criteria

* pregnancy
Minimum Eligible Age

15 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University Medical Centre Ljubljana

OTHER

Sponsor Role lead

Responsible Party

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University Medical Centre Ljubljana

Principal Investigators

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Franc Strle, MD PhD

Role: STUDY_CHAIR

UMC Ljubljana

Locations

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UMC Ljubljana, Department of Infectious Diseases

Ljubljana, , Slovenia

Site Status

Countries

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Slovenia

Central Contacts

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Katarina Ogrinc, MD PhD

Role: CONTACT

+386 1 522 4217

Franc Strle, PhD MD

Role: CONTACT

+386 1 522 2110

Other Identifiers

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POST-KME

Identifier Type: -

Identifier Source: org_study_id

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