ClinicalTrials.Veeva

Menu

Maternal Non-Stress Testing

Northwestern University logo

Northwestern University

Status

Completed

Conditions

Pregnant Women

Treatments

Device: wearable vital signs sensor

Study type

Observational

Funder types

Other

Identifiers

NCT04343482
STU00205895

Details and patient eligibility

About

Percent agreement of vital signs monitoring between the experimental sensor and standard of care monitoring

Enrollment

91 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Maternal age >18 years old
  • Pregnant mothers >26 weeks undergoing nonstress testing or delivering
  • Singleton pregnancy
  • No fetal abnormality or chromosomal abnormality
  • Subjects willing and able to comply with requirements of the protocol
  • Nurses and clinicians who will be administering the non-stress test to the pregnant subject

Exclusion criteria

  • Women who refuse to signed the informed consent form
  • Maternal age under 18 years old
  • Multiple pregnancy
  • Known major fetal malformation or chromosomal abnormality
  • Medical or obstetric problem that would preclude the use of abdominal electrodes
  • Inability to consent to this study due to medical illness, diminished intellectual capacity, or language barrier
  • Women using pacemakers

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems