Trial · NCT02299414
Outcomes33
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
1 to 20 of 33
Download this page as JSON| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Composite Adverse Perinatal Outcome | Up to 2 weeks postpartum for preeclampsia or 90 days for neonatal death | Participants | COUNT_OF_PARTICIPANTS | |
| PRIMARY | Small for Gestational Age (Safety) | Until delivery | Analysis is restricted to 2270 (1146 in the Treatment Group and 1124 in the Standard Group) who were delivered and who had complete assessments during delivery. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Composite of Maternal Death or Severe Cardiovascular Morbidity | Up to 6 weeks (4-12 weeks) after delivery | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Severe Maternal Hypertension + Components of the Primary Composite Endpoint | Up to 2 weeks postpartum or 90 days for neonatal death | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Preterm Birth and Indicated Preterm Birth (<37 Weeks) | Until delivery | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Composite of Severe Neonatal Morbidities | Up to 90 days post delivery | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Adherence to Treatment After Delivery | 6 weeks (4-12 weeks) after delivery | Analysis is restricted to 706 in Treatment Group and 479 in Standard Group who had complete antihypertensive therapy assessments at the follow-up study visit. | Participants | COUNT_OF_PARTICIPANTS |
| OTHER_PRE_SPECIFIED | Superimposed Preeclampsia | Up to 2 weeks after delivery | Participants | COUNT_OF_PARTICIPANTS | |
| OTHER_PRE_SPECIFIED | Superimposed Gestational Hypertension | Enrollment (between 6 and 18 weeks gestation) to delivery | Participants | COUNT_OF_PARTICIPANTS | |
| OTHER_PRE_SPECIFIED | Severe Hypertension | Up to 6 weeks (4-12 weeks) after delivery | Participants | COUNT_OF_PARTICIPANTS | |
| OTHER_PRE_SPECIFIED | Cesarean Delivery | Until delivery | Participants | COUNT_OF_PARTICIPANTS | |
| OTHER_PRE_SPECIFIED | Blood Transfusion | Up to 6 weeks | Participants | COUNT_OF_PARTICIPANTS | |
| OTHER_PRE_SPECIFIED | NICU Admission | Up to 6 weeks (4-12 weeks) after delivery | Participants | COUNT_OF_PARTICIPANTS | |
| OTHER_PRE_SPECIFIED | Low Birth Weight | At birth | Participants | COUNT_OF_PARTICIPANTS | |
| OTHER_PRE_SPECIFIED | Ponderal Index | At birth | data incomplete for 71 in the Treated Group and 83 in the Standard Group | g/cm^3 | MEAN |
| OTHER_PRE_SPECIFIED | Head Circumference | At birth | data incomplete for 84 in the Treated Group and 97 in the Standard Group | cm | MEAN |
| OTHER_PRE_SPECIFIED | Placental Weight | At delivery | data incomplete for 549 in the Treated Group and 562 in the Standard Group | g | MEAN |
| OTHER_PRE_SPECIFIED | Hypoglycemia | From delivery to hospital discharge (2 - 3 days after delivery) | Participants | COUNT_OF_PARTICIPANTS | |
| OTHER_PRE_SPECIFIED | Bradycardia | From delivery to hospital discharge (2 - 3 days after delivery) | Participants | COUNT_OF_PARTICIPANTS | |
| OTHER_PRE_SPECIFIED | Hypotension | From delivery to hospital discharge (2 - 3 days after delivery) | 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
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GET https://conductscience.org/api/trials/v1/NCT02299414/outcomes