Autopsy report · NCT02950896

Intraoperative Fetal Heart Rate (FHR) Monitoring: a Feasibility Study

Cause of deathOther Automatic label, confidence 0.3, unverified. How labels are made.

“Appropriate devices for fetal heart rate monitoring were not available.”

The sponsor’s own words in the registry.

Life of this trial

Ran for about 1 year before it stopped.
4 participants enrolled.
Results were posted on the registry 1 year 6 months after it ended.

Vital statistics

Status: Terminated
Sponsor: Washington University School of Medicine
Sponsor type: University, hospital or other
Conditions: Fetal Monitoring; Labor, Obstetric
Interventions: observational fetal heart rate monitoring
Participants: 4
Sites: 1
Countries: United States

Look deeper

The official registry record (the source of truth)
Record history: every change the sponsor made
Open it in the database

Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.