Trial · NCT05049616
Outcomes21
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
1 to 20 of 21
Download this page as JSON| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Number of Participants With Stage 2 Hypertension | 7-10 after delivery | Data were not collected for 1 participants in the Hctz/Lisionpril arm. Data were not collected for 8 participants in the extended release nifedipine arm. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants With Severe Postpartum Hypertension | 7-10 after delivery | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Number of Participants Who Received Additional Antihypertensive During Admission | 7-10 days postpartum | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Postpartum Length of Stay | up to 30 days after delivery | days | MEDIAN | |
| SECONDARY | Postpartum Readmission | up to 30 days after delivery | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Time to Blood Pressure Control | 10 days | Data were not collected for this outcome measure. | ||
| SECONDARY | Incidence of Persistent Postpartum Hypertension | 6 weeks postpartum | Data were not collected for this outcome measure. | ||
| SECONDARY | Occurrence of Proteinuria | 7-10 days, and 6 weeks postpartum | Data were not collected for this outcome measure | ||
| SECONDARY | Presense of Labs Abnormality | 7-10 days, and 6 weeks postpartum | Data were not collected for this outcome measure | ||
| SECONDARY | Compliance With Medications | at the time of the 1st postpartum clinic visit, which is about 6 to 37 days after birth | Data were not collected for 4 participants in the Hctz/Lisinopril arm. Data were not collected for 8 participants in the Extended release nifedipine arm | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Time to Control Blood Pressure | 3 month-1 year | Data were not collected for this outcome measure. | ||
| SECONDARY | Number of Patients Receiving Primary Care With BP Measurement | 1 year postpartum | Data were not collected for this outcome because participants were lost to follow up. | ||
| SECONDARY | Postpartum Complications- Number of Participants With ICU Admission | 10 days postpartum | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Postpartum Complications- Number of Participants With HELLP (Hemolysis, Elevated Liver Enzymes and Low Platelets) Syndrome | 10 days postpartum | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Postpartum Complications- Number of Participants With Eclampsia | 10 days postpartum | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Postpartum Complications- Number of Participants With Stroke | 10 days postpartum | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Postpartum Complications- Number of Participants With Renal Failure | 10 days postpartum | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Postpartum Complications- Number of Participants With Pulmonary Edema | 10 days postpartum | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Postpartum Complications - Number of Participants With Cardiomyopathy | 10 days postpartum | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Postpartum Complications- Number of Participants With Maternal Death | 10 days postpartum | Participants | COUNT_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.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT05049616/outcomes