Trial · NCT04615624
Registered outcomes21
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 20 of 21
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Mean Systolic Blood Pressure During Hour After Study Drug | 0 minutes to 60 minutes post-dose | Mean systolic blood pressure during hour after study drug administration. |
| Secondary | Mean Diastolic Blood Pressure During Hour After Study Drug | 0 minutes to 60 minutes post-dose | Mean diastolic blood pressure during the 1-hour period after drug administration. |
| Secondary | Change From Qualifying Systolic Blood Pressure | 0 minutes to 1 hour post-dose | Change from qualifying systolic blood pressure (qualifying SBP-mean SBP during hour after intervention) where qualifying systolic blood pressure refers to a severe range SBP (\>=160 millimeters of mercury (mmHg)) for at least 15 minutes. |
| Secondary | Change From Qualifying Diastolic Blood Pressure | 0 minutes to 1 hour post-dose | Change from qualifying diastolic blood pressure (qualifying DBP-mean DBP during hour after intervention) where qualifying diastolic blood pressure refers to a severe range DBP (\>=110 millimeters of mercury (mmHg)) for at least 15 minutes. |
| Secondary | Pulse Pressure at 2 Hours After Study Drug. | 2 hours post-dose | Pulse pressure at 2 hours after study drug. |
| Secondary | Systolic Blood Pressure at 2 Hours After Study Drug | 2 hours post-dose | Systolic blood pressure at 2 hours after study drug |
| Secondary | Diastolic Blood Pressure at 2 Hours After Study Drug | 2 hours post-dose | Diastolic blood pressure at 2 hours after study drug |
| Other | Gestational Age at Delivery | at the time of birth | Gestational age in weeks and days at the time of birth |
| Other | Time From Admission to Delivery | at the time of delivery | Time in days and hours from admission to birth |
| Other | Time From Treatment to Delivery | at the time of delivery | Time in days and hours from treatment to birth |
| Other | Induction of Labor | at the time of induction of labor | Number of women who required induction of labor |
| Other | Mode of Delivery | at time of delivery | Type of delivery |
| Other | Eclampsia | at time of hospital discharge | Number of women who developed seizure |
| Other | Low Apgar Scores of Neonate (Apgar Score <7 at 5 Min) | at 5 minutes after delivery | Neonatal clinical assessment (Apgar is not an abbreviated term). Minimum value 0; maximum value 9; Tool is used for assessment and not an accurate prognostic tool to predict outcomes. |
| Other | Newborns Admitted to Intensive Care Nursery | assessed from time of delivery until discharge since neonates can be admitted to the NICU at any time during this interval if issues arise. | Neonatal Intensive Care Unit admission |
| Other | Time 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. | Time to achieve first non-severe BP (m) |
| Other | Number of Participants Who Required Additional Antihypertensive Agents in an Hour After Allocation | Assessed from 0 minutes to 1 hour post-dose, 1-hour post-dose reported | Were any additional antihypertensive agents in hour after allocation |
| Other | Latency Until Next First-line Antepartum Antihypertensive Agents | 0 minutes to delivery of baby (72 hours post-dose) | time until next first-line antepartum antihypertensive agent given |
| Other | Discharged Without Delivery | at time of hospital discharge | proportion of participants who were discharged prior to delivery of the baby |
| Other | Length of Stay | at time of hospital discharge | length of stay |
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.
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GET https://conductscience.org/api/trials/v1/NCT04615624/registered