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Trial · NCT02014519

Outcomes37

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYNumber of Seropositive Subjects in Terms of Anti-pertussis Toxin (Anti-PT) ConcentrationsAt the time of enrollment of each subject (Day 0)The analysis was performed on the According-to-Protocol (ATP) cohort included all evaluable subjects for whom valid laboratory test results for anti-pertussis toxin antibodies were available.ParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYNumber of Subjects With Anti-PT IgG Levels Strongly Indicative of Current/Recent InfectionAt the time of enrollment of each subject (Day 0)The analysis was performed on the According-to-Protocol (ATP) cohort included all evaluable subjects for whom valid laboratory test results for anti-pertussis toxin antibodies were available.ParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYNumber of Subjects With Anti-PT IgG Levels Indicative of Current/Recent InfectionAt the time of enrollment of each subject (Day 0)The analysis was performed on the According-to-Protocol (ATP) cohort included all evaluable subjects for whom valid laboratory test results for anti-pertussis toxin antibodies were available.ParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYNumber of Seronegative Subjects in Terms of Anti-PT ConcentrationsAt the time of enrollment of each subject (Day 0)The analysis was performed on the According-to-Protocol (ATP) cohort included all evaluable subjects for whom valid laboratory test results for anti-pertussis toxin antibodies were available.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Seropositive Subjects in Terms of Anti-PT Concentrations (by Age)At the time of enrollment of each subject (Day 0).The analysis was performed on the According-to-Protocol (ATP) cohort included all evaluable subjects for whom valid laboratory test results for anti-pertussis toxin antibodies were available.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Subjects With Anti-PT IgG Levels Strongly Indicative of Current/Recent Infection (by Age)At the time of enrollment of each subject (Day 0)The analysis was performed on the According-to-Protocol (ATP) cohort included all evaluable subjects for whom valid laboratory test results for anti-pertussis toxin antibodies were available.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Subjects With Anti-PT IgG Levels Indicative of Current/Recent Infection (by Age)At the time of enrollment of each subject (Day 0)The analysis was performed on the According-to-Protocol (ATP) cohort included all evaluable subjects for whom valid laboratory test results for anti-pertussis toxin antibodies were available.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Seronegative Subjects in Terms of Anti-PT Concentrations (by Age)At the time of enrollment of each subject (Day 0)The analysis was performed on the According-to-Protocol (ATP) cohort included all evaluable subjects for whom valid laboratory test results for anti-pertussis toxin antibodies were available.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Seropositive Subjects in Terms of Anti-PT Concentrations (by Gender)At the time of enrollment of each subject (Day 0)The analysis was performed on the According-to-Protocol (ATP) cohort included all evaluable subjects for whom valid laboratory test results for anti-pertussis toxin antibodies were available.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Subjects With Anti-PT IgG Levels Strongly Indicative of Current/Recent Infection (by Gender)At the time of enrollment of each subject (Day 0)The analysis was performed on the According-to-Protocol (ATP) cohort included all evaluable subjects for whom valid laboratory test results for anti-pertussis toxin antibodies were available.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Subjects With Anti-PT IgG Levels Indicative of Current/Recent Infection (by Gender)At the time of enrollment of each subject (Day 0)The analysis was performed on the According-to-Protocol (ATP) cohort included all evaluable subjects for whom valid laboratory test results for anti-pertussis toxin antibodies were available.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Seronegative Subjects in Terms of Anti-PT Concentrations (by Gender)At the time of enrollment of each subject (Day 0)The analysis was performed on the According-to-Protocol (ATP) cohort included all evaluable subjects for whom valid laboratory test results for anti-pertussis toxin antibodies were available.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Subjects With Anti-PT IgG Levels Not Indicative of Current/Recent Infection (by Gender)At the time of enrollment of each subject (Day 0)The analysis was performed on the According-to-Protocol (ATP) cohort included all evaluable subjects for whom valid laboratory test results for anti-pertussis toxin antibodies were available.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Seropositive Subjects in Terms of Anti-PT Concentrations (by Recent History of Long-lasting Cough)At the time of enrollment of each subject (Day 0)
The analysis was performed on the According-to-Protocol (ATP) cohort included all evaluable subjects for whom valid laboratory test results for anti-pertussis toxin antibodies were available and who provided information on recent history of long-lasting cough.
ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Seronegative Subjects in Terms of Anti-PT Concentrations (by Recent History of Long-lasting Cough)At the time of enrollment of each subject (Day 0)
The analysis was performed on the According-to-Protocol (ATP) cohort included all evaluable subjects for whom valid laboratory test results for anti-pertussis toxin antibodies were available and who provided information on recent history of long-lasting cough.
ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Subjects With Anti-PT IgG Levels Indicative of Current/Recent Infection (by Recent History of Long-lasting Cough)At the time of enrollment of each subject (Day 0)
The analysis was performed on the According-to-Protocol (ATP) cohort included all evaluable subjects for whom valid laboratory test results for anti-pertussis toxin antibodies were available and who provided information on recent history of long-lasting cough.
ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Subjects With Anti-PT IgG Levels Not Indicative of Current/Recent Infection (by Recent History of Long-lasting Cough)At the time of enrollment of each subject (Day 0)
The analysis was performed on the According-to-Protocol (ATP) cohort included all evaluable subjects for whom valid laboratory test results for anti-pertussis toxin antibodies were available and who provided information on recent history of long-lasting cough.
ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Seropositive Subjects in Terms of Anti-PT Concentrations (by Smoking Status)At the time of enrollment of each subject (Day 0)The analysis was performed on the According-to-Protocol (ATP) cohort included all evaluable subjects for whom valid laboratory test results for anti-pertussis toxin antibodies were available.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Seronegative Subjects in Terms of Anti-PT Concentrations (by Smoking Status)At the time of enrollment of each subject (Day 0)The analysis was performed on the According-to-Protocol (ATP) cohort included all evaluable subjects for whom valid laboratory test results for anti-pertussis toxin antibodies were available.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Subjects With Anti-PT IgG Levels Indicative of Current/Recent Infection (by Smoking Status)At the time of enrollment of each subject (Day 0)The analysis was performed on the According-to-Protocol (ATP) cohort included all evaluable subjects for whom valid laboratory test results for anti-pertussis toxin antibodies were available.ParticipantsCOUNT_OF_PARTICIPANTS

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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