ConductScience.org, home

Trial · NCT02641340

Registered outcomes13

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryMaximum concentration (Cmax)within 24 hours (see detailed description)
PrimaryTime to reach peak or maximum concentration following drug administration (Tmax)within 24 hours (see detailed description)
PrimaryArea under the concentration-time curvewithin 24 hours (see detailed description)Categories: during a dosing interval (AUCtau ), from the time of dosing to infinity (AUC0-inf), from the time of dosing to the last quantifiable time point (AUC0-t)
PrimaryApparent elimination rate constant in the terminal phase by non-compartmental analysiswithin 24 hours (see detailed description)
PrimaryCorresponding half-life (t1/2)within 24 hours (see detailed description)
PrimaryTrough concentration during multiple dosing prior to next dose (Ctrough)within 24 hours (see detailed description)
PrimaryAccumulation ratioswithin 24 hours (see detailed description)Categories: of Cmax (ARcmax), based on trough concentration (ARctrough), of AUCtau (ARauctau)
PrimaryDose normalized Cmaxwithin 24 hours (see detailed description)
PrimaryDose normalized AUCwithin 24 hours (see detailed description)Categories: AUC0-1, AUC0-inf, AUCtau
SecondaryParticipants with respiratory depression requiring the use of naloxonewithin 24 hours
SecondaryParticipants with hypoxia requiring oxygen administrationwithin 24 hours
SecondaryParticipants needing noninvasive respiratory maneuvers (e.g., jaw thrust, bag-valve mask) to improve respiratory status at any point during the studywithin 24 hours
SecondaryParticipants with hypotension requiring interventionwithin 24 hours

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.

For software

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT02641340/registered