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NCT07795320Not yet recruiting

Cerebroplacental Ratio (CPR) and Amniotic-Umbilical-to-Cerebral Ratio (AUCR), in in Women With Hypertensive Disorders of Pregnancy.

Comparison Between Cerebroplacental Ratio (CPR) and Amniotic-Umbilical-to-Cerebral Ratio (AUCR), in Predicting of Adverse Perinatal Outcome in Women With Hypertensive Disorders of Pregnancy.

Source: ClinicalTrials.gov · Last updated 31 Aug 2026

Brief summary (registry, in English)

The primary aim of this study is to evaluate the predictive value of the Amniotic-Umbilical-to-Cerebral Ratio (AUCR) in predicting composite adverse perinatal outcomes in women with hypertensive disorders of pregnancy and to compare its predictive performance with the traditional Cerebroplacental Ratio (CPR)

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
130 (estimated)
First submitted
23 Aug 2026
Start date
1 Nov 2026
Primary completion date
1 Apr 2028
Lead sponsor
Assiut University
NCT number
NCT07795320

What you commit to

  • Study type: Observational
  • Planned participants: 130
  • From 1 Nov 2026 to the primary completion date, 1 Apr 2028
  • No sites listed in no 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

  • Maternal diseases likely to independently affect fetal circulation or perinatal outcome, such as significant cardiac disease or other major systemic diseases.

Other

  • Multiple gestation.
  • Fetuses with known chromosomal or major congenital anomalies.
  • Inability to complete the required follow-up.

Who the study is looking for

  • Women aged 18-40 years, inclusive.
  • Singleton viable pregnancy.
  • Gestational age ≥32 weeks.
  • Pregnancy complicated by a hypertensive disorder.
  • Women who provide written informed consent.

Age in the registry: 18 years to 40 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

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