ConductScience.org, home

Trial · NCT04615624

Outcomes21

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYMean Systolic Blood Pressure During Hour After Study Drug0 minutes to 60 minutes post-dosemmHgMEAN
SECONDARYMean Diastolic Blood Pressure During Hour After Study Drug0 minutes to 60 minutes post-dosemmHgMEAN
SECONDARYChange From Qualifying Systolic Blood Pressure0 minutes to 1 hour post-dosemmHgMEAN
SECONDARYChange From Qualifying Diastolic Blood Pressure0 minutes to 1 hour post-dosemmHgMEAN
SECONDARYPulse Pressure at 2 Hours After Study Drug.2 hours post-doseNot every participant had their blood pressure and thus pulse pressure checked at 2 hours which is a limitation of the study.mmHgMEAN
SECONDARYSystolic Blood Pressure at 2 Hours After Study Drug2 hours post-doseNot every participant had their blood pressure checked at 2 hours which is a limitation of the study.mmHgMEAN
SECONDARYDiastolic Blood Pressure at 2 Hours After Study Drug2 hours post-doseNot every participant had their blood pressure checked at 2 hours which is a limitation of the study.mmHgMEAN
OTHER_PRE_SPECIFIEDGestational Age at Deliveryat the time of birthweeksMEAN
OTHER_PRE_SPECIFIEDTime From Admission to Deliveryat the time of deliverydaysMEDIAN
OTHER_PRE_SPECIFIEDTime From Treatment to Deliveryat the time of deliverydaysMEDIAN
OTHER_PRE_SPECIFIEDInduction of Laborat the time of induction of laborParticipantsCOUNT_OF_PARTICIPANTS
OTHER_PRE_SPECIFIEDMode of Deliveryat time of deliveryParticipantsCOUNT_OF_PARTICIPANTS
OTHER_PRE_SPECIFIEDEclampsiaat time of hospital dischargeParticipantsCOUNT_OF_PARTICIPANTS
OTHER_PRE_SPECIFIEDLow Apgar Scores of Neonate (Apgar Score <7 at 5 Min)at 5 minutes after deliveryneonatesNUMBER
OTHER_PRE_SPECIFIEDNewborns Admitted to Intensive Care Nurseryassessed from time of delivery until discharge since neonates can be admitted to the NICU at any time during this interval if issues arise.neonatesNUMBER
OTHER_PRE_SPECIFIEDTime to Achieve First Non-severe BP (m)Assessed from time of severe range blood pressure to time at resolution of severe range blood pressure. Reported at time of resolution of severe range blood pressure.minutesMEDIAN
OTHER_PRE_SPECIFIEDNumber of Participants Who Required Additional Antihypertensive Agents in an Hour After AllocationAssessed from 0 minutes to 1 hour post-dose, 1-hour post-dose reportedParticipantsCOUNT_OF_PARTICIPANTS
OTHER_PRE_SPECIFIEDLatency Until Next First-line Antepartum Antihypertensive Agents0 minutes to delivery of baby (72 hours post-dose)Those who required additional medication (not all participants required additional antihypertensive medication).hoursMEDIAN
OTHER_PRE_SPECIFIEDDischarged Without Deliveryat time of hospital dischargeParticipantsCOUNT_OF_PARTICIPANTS
OTHER_PRE_SPECIFIEDLength of Stayat time of hospital dischargedaysMEDIAN

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/NCT04615624/outcomes