UnknownNot Applicable

Study on Early Lyme Neuroborreliosis

Slovenia50 participantsStarted 2009-01-01

Plain-language summary

The purpose of this study is to determine clinical course and the sequelae of early Lyme neuroborreliosis after treatment with ceftriaxone.

Who can participate

Age range15 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * erythema migrans within 4 months before neurologic involvement and pleocytosis in patients \>15 years old Exclusion Criteria: * pregnancy * lactation * history of adverse reaction to a beta-lactam antibiotic

What they're measuring

Objective sequelae and post-treatment subjective symptoms in patients treated with ceftriaxone for early Lyme neuroborreliosis

Timeframe: 1 year follow-up

Trial details

NCT IDNCT00910533

SponsorUniversity Medical Centre Ljubljana

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2018-12-31

Contact for this trial

Dasa Stupica, MD

+38615222110 cerar.dasa@gmail.com

View on ClinicalTrials.gov More Nervous System Lyme Borreliosis trials