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Completed

NCT Number: NCT03497572

Seroprevalence Study to Evaluate the Persistence of Anti-leptospira Antibody in Subjects Vaccinated With Spirolept® Vaccine

The study aims to assess antibody persistence induced by Spirolept® vaccination in subjects who received at least 4 doses (2 doses two weeks apart and 2 booster doses) and no more than a total of 8 doses (2 doses two weeks apart and 6 booster doses).

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

SIAAP, Maisons-Laffitte, France

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About this study

This is a seroprevalence, phase IV, multi -center study to evaluate anti-Leptospira antibody persistence in subjects who have received at least the 2nd booster (4 vaccine doses) and no more than the 6th booster (8 vaccine doses) of Spirolept® vaccine.

The study will be conducted at the Occupational Health Centre of companies employing workers at risk of leptospirosis for their occupational activities. Study participants will be selected from the company Occupational Health Centre database where each employee is registered. All workers are regularly followed-up and their medical and vaccination history recorded. Subjects selection will occur according the number of booster doses received (having received at least the 2nd booster and no more than the 6th booster). After they have signed the informed consent form, subjects will be recruited into the study and if all inclusion and exclusion criteria are met they will be taken a blood sample.

Anti-leptospira IgG antibody will be measured by a validated ELISA. Other assay may be performed to further characterize anti-leptospira antibodies. Data on subject demographics, relevant medical history, vaccination dates, and blood collection will be recorded in an appropriate Case Report Form.

The study does not include any vaccination.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Adults of both genders aged 18 to 65 years
  • High risk occupational subjects to leptospirosis having received at least 4 (2 initial doses and 2 booster doses) and no more than 8 (2 first doses and 6 booster doses) doses of Spirolept®
  • Previous Spirolept® vaccination dates documented
  • To be affiliated to a health insurance plan
  • Having signed the informed consent form

Exclusion criteria

  • Had an acute infection during the 3 weeks before study enrollment
  • Subject with documented HIV or hepatitis A, B, C
  • Immunosuppressive treatment (chemotherapy, corticosteroids > 20mg/day, biological agents)
  • Subject with progressive malignancy requiring specific treatment
  • Previous documented Leptospirosis

Treatment and study plan

Primary outcomes

  1. ELISA immunoglobulin G (IgG) anti-leptospire

    Time frame: through study completion, an average of 8 months

    Proportion of subjects seropositive to ELISA IgG anti-leptospira (with cut-off antibody titer ≥ 20) at different time points after the last booster dose

Secondary outcomes

  1. ELISA IgG geometric mean titer (GMTs)

    Time frame: through study completion, an average of 8 months

    Proportion of subjects seropositive to ELISA IgG anti-leptospira (with cut-off antibody titer ≥ 20) and GMTs at different time points according to demographic factors and vaccination scheme

Other outcomes

  1. exploratory growth inhibition test (GIT) Test

    Time frame: through study completion, an average of 8 months

    Proportion of subjects with positive GIT (positive GIT: serum that provides ≥ 50% leptospira growth inhibition in the test)

Sponsors and collaborators

Lead sponsor

Imaxio

Industry

Registry information

Official study title

Seroprevalence, Multi-center, Phase IV Cross-sectional Study to Evaluate the Persistence of Anti-leptospira Antibody in Subjects Vaccinated With Spirolept® Vaccine

Acronym: SPT-001

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Apr 13, 2018
Registry last updated
May 8, 2018

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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