CompletedNot Applicable

Fetal Intrapartum Heart Rate FHR/ECG Study

United States400 participantsStarted 2013-03

Plain-language summary

The objective of the study is to evaluate the association between certain markers in the blood of neonatal brain injury and specific Fetal Heart Rate monitoring findings using the device under study.

Who can participate

Age range18 Years

SexFEMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Pregnant women in their third trimester and Women in labor (the progressive effacement and dilatation of the cervix) who are having their fetus' heart rate monitored continuously will form the eligible population for recruitment into our study * 18 years old or older * Women with the diagnosis of fetal intrauterine growth restriction may be included. Exclusion Criteria: * Speakers of languages other than English * Gestational age less than 24 weeks 0 days

What they're measuring

Quantitative FHR patterns predictive of adverse neonatal outcome

Timeframe: During Labor

Trial details

NCT IDNCT01881685

SponsorMindchild Medical Inc.

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2015-12

View on ClinicalTrials.gov More Abnormality in Fetal Heart Rate or Rhythm trials