Trial · NCT07894705
Blood Pressure Goal in Preterm Preeclampsia
NCT07894705, Not yet recruiting, Ohio State University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Blood Pressure Goal in Preterm Preeclampsia. Trials, record NCT07894705. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07894705
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Blood Pressure Goal in Preterm Preeclampsia
- NCT number
- NCT07894705
- Status
- Not yet recruiting
- Enrollment
- 68 participants, estimated
- Lead sponsor
- Ohio State University
- Conditions
- Hypertensive Disorder of Pregnancy, Preeclampsia
- Interventions
- Treating BP acutely with intravenous or rapid acting oral medications
- First posted
- 2026-10-26
- Last updated
- 2026-10-26
Source ClinicalTrials.gov
Registered outcomes38
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Mean latency from diagnosis of hypertensive disorders of pregnancy (HDP) to delivery (continuous, mean with standard deviation) | from randomization to delivery | The number of days from randomization to delivery will be analyzed as a continuous variable |
| Secondary | Blood pressure control (continuous, mean with standard deviation) | from randomization to delivery | BP control will be analyzed as mean systolic and diastolic blood pressures; frequency of acute treatment (oral or IV) of severe range elevated BPs |
| Secondary | Serum Soluble fms-like tyrosine kinase 1 / placental growth factor (sFlt-1/PlGF) (log ratio) | from randomization to delivery | Weekly serum sFlt-1/PlGF will be obtained from randomization until delivery. The clinical care team will be blinded to the results of this test as this is not part of our institutional protocol for inpatient management of HDP. The results will be analyzed at the conclusion of the study. |
| Secondary | The frequency of hemolysis, elevated liver enzymes, low platelets (HELLP) | from randomization through 6 weeks postpartum | |
| Secondary | Frequency of placental abruption | from randomization to delivery | |
| Secondary | Frequency of eclampsia | from randomization through 6 weeks postpartum | |
| Secondary | Frequency of stroke | from randomization through 6 weeks postpartum | |
| Secondary | Frequency of MI or angina | from randomization through 6 weeks postpartum | |
| Secondary | Frequency of heart failure | from randomization through 6 weeks postpartum | |
| Secondary | Frequency of intensive care unit (ICU) admission or intubation | from randomization through 6 weeks postpartum |
1 to 10 of 38Source ClinicalTrials.gov
See all 38 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
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 trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07894705
GET https://conductscience.org/api/trials/v1/NCT07894705/registered?page=2