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OpenTrials
Completed

NCT Number: NCT00138801

Effect of Intravenous Ceftriaxone and Oral Doxycycline for Lyme Neuroborreliosis

The aim of this study is to compare parenteral ceftriaxone and oral doxycycline in the treatment of neuroborreliosis in a randomized controlled trial.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Neurological symptoms and/or findings consistent with neuroborreliosis and at least one of the following fulfilled:
  • Intrathecal production of borrelia antibodies;
  • White cell count in cerebrospinal fluid (CSF) > 5/mm3;
  • Significant rise in borrelia antibodies in two serum samples collected from a patient with at least 3 weeks interval;
  • Verified acrodermatitis chronica atrophicans.

Exclusion criteria

  • Allergy to the contents in the medication, or earlier type I reaction to penicillin.
  • Treatment with cephalosporins, penicillin or tetracyclins during the last 14 days
  • Pregnancy or breastfeeding
  • Age < 18 years

Treatment and study plan

Ceftriaxone

Drug

Doxycycline

Drug

Sponsors and collaborators

Lead sponsor

Sorlandet Hospital HF

Other Gov

Registry information

Official study title

Effect of Intravenous Ceftriaxone and Oral Doxycycline for Lyme Neuroborreliosis. A Randomized Double-blind Comparison

Important dates

Study start
2004
Primary completion
2008
Study completion
2008
First posted
Aug 30, 2005
Registry last updated
May 6, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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