Status:
TERMINATED
Mobile Phone Application Versus Handheld Device for Fetal Vibroacoustic Stimulation
Lead Sponsor:
Wayne State University
Conditions:
Pregnancy
Eligibility:
FEMALE
18-50 years
Phase:
NA
Brief Summary
This is a randomized controlled single blinded crossover study to compare fetal vibroacoustic stimulation with a handheld device to a mobile phone application designed for this study. The handheld dev...
Detailed Description
There are multiple proposed methods of assessing fetal well-being in utero. One such method which has been well accepted for fetal surveillance is the non-stress test (NST), during which the fetal hea...
Eligibility Criteria
Inclusion
- Pregnant patients at 32 to 42 weeks gestation who are already undergoing fetal heart rate monitoring in the hospital setting at Hutzel Hospital in Detroit, Michigan in triage, the antepartum floor, or on labor and delivery.
Exclusion
- Clinically unstable patients, patient who have been on magnesium sulfate or had opioid administration within the last 4 hours, fetuses with intrauterine growth restriction, patients contracting more than 3 times in 10 minutes, and twin pregnancies or higher order multiples.
Key Trial Info
Start Date :
March 1 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2019
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT03446248
Start Date
March 1 2018
End Date
January 1 2019
Last Update
April 29 2019
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Hutzel Hospital
Detroit, Michigan, United States, 48201