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NCT06045481

Postexposure Prophylaxis With Single Dose Doxycycline for the Prevention of Tick-borne Relapsing Fever

Not yet recruiting NA Last updated 13 March 2024
What this trial tests

NA trial testing administration of single dose of doxycycline in Relapsing Fever, Tick-Borne in 526 participants. Not yet recruiting.

Timeline
1 August 2024
Primary endpoint
31 October 2026
31 October 2027

Quick facts

Lead sponsorMedical Corps, Israel Defense Force
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment526
Start date1 August 2024
Primary completion31 October 2026
Estimated completion31 October 2027

Drugs / interventions tested

Conditions studied

Sponsor

Medical Corps, Israel Defense Force — full company profile →

Who can join

Adults 18 to 30, any sex, with Relapsing Fever, Tick-Borne. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this clinical trial is to compare standard treatment (5 days of doxycycline) vs single dose doxycycline for the prevention of tick-borne relapsing fever in soldiers who found bite marks on their bodies after an activity that includes contact with the ground or staying at a site suspected of being infected with ticks. The main question\[s\] it aims to answer are: * Testing whether preventive treatment with a single dose of doxylin at a dose of 200 mg is effective in preventing recurrent fever, and if so, at what rate * Checking the profile and rate of side effects in each one of the proposed treatment protocols Participants will be treated with standard treatment (5 days of doxycycline) or single dose doxycycline.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Medical Corps, Israel Defense Force trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06045481.

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