Trial Outcomes & Findings for Intraoperative Fetal Heart Rate (FHR) Monitoring: a Feasibility Study (NCT NCT02950896)
NCT ID: NCT02950896
Last Updated: 2019-05-10
Results Overview
This measure will be compared to the acoustic monitoring of FHR across the same 10 minutes.
Recruitment status
TERMINATED
Target enrollment
4 participants
Primary outcome timeframe
10 minutes of evaluable ECG reading
Results posted on
2019-05-10
Participant Flow
Participant milestones
| Measure |
Intraoperative FHR Monitoring
Intraoperative fetal heart rate (FHR) monitoring
observational fetal heart rate monitoring: Patients will have fetal heart rate monitoring
|
|---|---|
|
Overall Study
STARTED
|
4
|
|
Overall Study
COMPLETED
|
4
|
|
Overall Study
NOT COMPLETED
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Intraoperative Fetal Heart Rate (FHR) Monitoring: a Feasibility Study
Baseline characteristics by cohort
Baseline data not reported
PRIMARY outcome
Timeframe: 10 minutes of evaluable ECG readingPopulation: The study was terminated and no results were analyzed.
This measure will be compared to the acoustic monitoring of FHR across the same 10 minutes.
Outcome measures
Outcome data not reported
Adverse Events
Intraoperative FHR Monitoring
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Heather McKenzie
Washington University School of Medicine
Phone: 3142862628
Email: [email protected]
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place