Trial · NCT00135707
Outcomes38
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
1 to 20 of 38
Download this page as JSON| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Composite of Pregnancy-associated Hypertension and Serious Adverse Outcomes in the Mother or Fetus or Neonate | 20 weeks through discharge following delivery | The analysis was intent to treat. | Participants | COUNT_OF_PARTICIPANTS |
| PRIMARY | Severe Hypertension | 20 weeks through discharge following delivery | Participants | COUNT_OF_PARTICIPANTS | |
| PRIMARY | Severe or Mild Pregnancy-associated Hypertension With Elevated Liver Enzyme Levels | 20 weeks through discharge following delivery | Participants | COUNT_OF_PARTICIPANTS | |
| PRIMARY | Severe or Mild Pregnancy-associated Hypertension With Thrombocytopenia | 20 weeks through discharge following delivery | participants | NUMBER | |
| PRIMARY | Severe or Mild Pregnancy-associated Hypertension With an Elevated Serum Creatinine Level | 20 weeks through discharge following delivery | Participants | COUNT_OF_PARTICIPANTS | |
| PRIMARY | Severe or Mild Pregnancy-associated Hypertension With an Eclamptic Seizure | 20 weeks through discharge following delivery | Participants | COUNT_OF_PARTICIPANTS | |
| PRIMARY | Severe or Mild Pregnancy-associated Hypertension With an Indicated Preterm Birth Before 32 Weeks of Gestation Owing to Hypertension-related Disorders | 20 weeks through discharge following delivery | Participants | COUNT_OF_PARTICIPANTS | |
| PRIMARY | Severe or Mild Pregnancy-associated Hypertension With a Fetus That Was Small for Gestational Age (Below the 3rd Percentile) Adjusted for Sex and Race or Ethnic Group | 20 weeks through discharge following delivery | Participants | COUNT_OF_PARTICIPANTS | |
| PRIMARY | Severe or Mild Pregnancy-associated Hypertension With a Fetal Death After 20 Weeks of Gestation or Neonatal Death | 20 weeks through discharge or prior to discharge following delivery admission | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Preeclampsia (Mild, Severe, HELLP Syndrome, Eclampsia) | 20 weeks through discharge following delivery | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Pregnancy Associated Hypertension | 20 weeks through discharge following delivery | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Medically Indicated Delivery Because of Hypertension | 20 weeks through discharge following delivery | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Aspartate Aminotransferase ≥100 U/Liter | 20 weeks through discharge | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Creatinine ≥1.5 mg/dl (133 μmol/Liter) | 20 weeks through discharge | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Antepartum Bleeding | During pregnancy | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Premature Rupture of Membranes | During pregnancy | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Placental Abruption | During pregnancy | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Cesarean Delivery | Delivery | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Maternal Death | Delivery through hospital discharge | One maternal death in each group due to peripartum cardiomyopathy. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Postpartum Pulmonary Edema | After delivery through discharge | Participants | COUNT_OF_PARTICIPANTS |
Source ClinicalTrials.govtrials-2026-11-12-0.4.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNone 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/NCT00135707/outcomes