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Completed

NCT Number: NCT02808494

Development of a Next Generation Sequencing (NGS) -Based Assay to Detect Preeclampsia Molecular Markers

Sample Collection Study

Completed

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Christiana Hospital, Newark, Delaware, United States

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About this study

This is a limited prospective collection of whole blood samples from pregnant women with a diagnosis of preeclampsia with severe features and/or fetal growth restriction in addition to samples from a control group to aid in the development of a Next Generation Sequencing (NGS)-based assay to detect molecular markers associated with preterm preeclampsia.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women 18 years of age or older at enrollment
  • Pregnant women with a viable singleton gestation
  • Able to provide written, informed consent
  • Able to provide 20 mL of whole blood
  • Diagnosis of preeclampsia with severe features and/or diagnosis of fetal growth restriction.
  • Preeclampsia with severe features is defined as:

Proteinuria: Excretion of ≥300mg/24hr (24 hour collection) of protein or a timed excretion that is extrapolated to the 24 hour urine value or a protein/creatinine [both in mg/dL] ratio of at least 0.3 or a qualitative determination of (urine dipstick) of ≥1+ WITH Systolic BP ≥160mmHg or diastolic BP ≥110mmHg on at least 2 occasions 4 hours apart while on bedrest but before the onset of labor OR Systolic BP ≥160mmHg or diastolic BP ≥110mmHg on 1 occasion but before the onset of labor, if antihypertensive therapy is initiated due to severe hypertension OR New onset hypertension defined as: Systolic BP ≥140 mmHg or diastolic ≥90 mmHg with one or more of the following features: Thrombocytopenia (<100,000 plts/mL); impaired liver function (AST/ALT 2X ULN); newly developed renal insufficiency (serum creatinine >1.1mg/dL or a doubling of serum creatinine in the absence of other renal disease); pulmonary edema; new onset cerebral disturbances or scotomata

  • Fetal Growth Restriction defined as:

Estimated fetal weight by ultrasound at ≥ 19 0/7 weeks gestational age < 5%ile or 5-10%ile with abnormal umbilical artery Doppler examination (S/D ratio >95%ile for gestational age, absent end diastolic flow or reverse end diastolic flow)

  • Gestational age between 20 0/7 and 33 6/7 weeks determined by ultrasound and/or LMP per ACOG guidelines1. A subject diagnosed with preeclampsia without severe features prior to 33 6/7 weeks gestation and who is managed expectantly and develops severe features after 34 weeks may be included.

Exclusion criteria

  • Known malignancy
  • History of maternal organ or bone marrow transplant
  • Maternal blood transfusion in the last 8 weeks
  • Chronic hypertension diagnosed prior to current pregnancy
  • Type I, II or gestational diabetes
  • Fetal anomaly or known chromosome abnormality
  • Active labor

Treatment and study plan

Primary outcomes

  1. cfRNA markers associated with preeclampsia with severe features and/or fetal growth restrictions

    Time frame: 2 years

Sponsors and collaborators

Lead sponsor

Illumina, Inc.

Industry

Registry information

Official study title

Prospective Collection of Whole Blood Specimens of Subjects Diagnosed With Preeclampsia With Severe Features and/or Fetal Growth Restriction in Support of a Molecular Assay Development

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Jun 21, 2016
Registry last updated
Apr 29, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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