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NCT07894705Not yet recruiting

Blood Pressure Goal in Preterm Preeclampsia

Blood Pressure Goal in Preterm Preeclampsia (BLiPP)

Source: ClinicalTrials.gov · Last updated 26 Oct 2026

Brief summary (registry, in English)

The purpose of this study is to compare latency (prolongation of pregnancy from diagnosis till delivery) in patients with hypertensive disorders of pregnancy (HDP) with severe features \< 34 weeks gestational age (GA), undergoing expectant management between tight and permissive blood pressure (BP) groups.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
68 (estimated)
First submitted
6 Oct 2026
Start date
Nov 2026
Primary completion date
Dec 2027
Lead sponsor
Ohio State University
NCT number
NCT07894705

What you commit to

  • Study type: Observational
  • Planned participants: 68
  • From Nov 2026 to the primary completion date, Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Poorly controlled preexisting chronic hypertension on ≥2 oral antihypertensive medications

Lab values

  • Preexisting CKD with serum creatinine \> 1.0

Other

  • HDP with severe features \> 32 weeks gestation at the time of admission
  • Contraindications to expectant management of preeclampsia with severe features per ACOG (attached)
  • Severe FGR (EFW \< 3rd percentile) or FGR with umbilical artery doppler abnormalities (absent or reversed end diastolic flow) at the time of enrollment
  • Multiple gestation
  • Major fetal anomaly (attached)
  • PPROM/active preterm labor

Who the study is looking for

  • Pregnant individuals
  • Age ≥ 18 years old
  • HDP with severe features
  • Planned inpatient admission for expectant management until delivery
  • GA 24 - ≤ 32 weeks GA
  • Singleton, non-anomalous fetus
  • Anticipated delivery at the study institution

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ohio State University Wexner Medical Center
Coordinator of this site? Confirm its status
ColumbusUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.