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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03838965
Other study ID # 0101-18-HYMC
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2019
Est. completion date December 16, 2020

Study information

Verified date June 2022
Source Hillel Yaffe Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The Effects of Labor Stages and Interventions on Hemodynamic Measures During and After Childbirth ( Epidural, Rupture Membranses Cesarean Sections and Preeclampsia) With Noninvasive Sensors.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date December 16, 2020
Est. primary completion date December 16, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Pregnant woman between 18-45 years old - with non cardiovascular disease Exclusion Criteria: - woman with a cardiovascular disease - woman who don't agree to participate in the trial

Study Design


Related Conditions & MeSH terms


Intervention

Device:
biobeat sensor
biobeat sensor is a noninvasive sensor of the the hymodynamic measures during the childbirth and after 24 hours.

Locations

Country Name City State
Israel Hillel Yaffe Medical Center Hadera

Sponsors (1)

Lead Sponsor Collaborator
Hillel Yaffe Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary biobeat sensor is a noninvasive sensor of the the hymodynamic measures during the childbirth biobeat sensor is a noninvasive sensor of the the hymodynamic measures during the childbirth 24 hours
Secondary biobeat sensor is a noninvasive sensor of the the hymodynamic measures after 24 hours of the childbirth biobeat sensor is a noninvasive sensor of the the hymodynamic measures after 24 hours of the childbirth 24 hours
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