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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03741569
Other study ID # 2017_63
Secondary ID 2018-A01194-51
Status Completed
Phase N/A
First received
Last updated
Start date October 17, 2017
Est. completion date July 17, 2022

Study information

Verified date December 2022
Source University Hospital, Lille
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The CIC-IT 1403 laboratory of the University Hospital of Lille has developed a technological solution for acquiring and synchronizing abdominal ECG, acoustic and Doppler signals. The purpose of this clinical trial is to build a database of signals issued from this device to develop signal processing algorithms to allow optimization of the fetal heart rate calculation. This study will be carried out in the maternity ward of the Jeanne de Flandre Hospital in the maternal-fetal pathology department Doppler, ECG and acoustic sensors will be placed on the mother's abdomen to capture the heart rate of the fetus and mother as well as uterine contractions. For each of the participants, we will make two 15-minute recordings: one with conventional ECG electrodes and one with ECG textile electrodes. This procedure will not affect the usual care of the patient


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date July 17, 2022
Est. primary completion date June 14, 2022
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - Pregnant woman - Age>18 years Exclusion Criteria: - Multiple pregnancy - Medical termination of pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Transabdominal Fetal Heart Rate
Doppler, ECG and acoustic sensors will be placed on the mother's abdomen to capture the heart rate of the fetus and mother as well as uterine contractions. For each of the participants, we will make two 15-minute recordings: one with conventional ECG electrodes and one with ECG textile electrodes

Locations

Country Name City State
France Hôpital Roger Salengro, CHU Lille

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Lille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary The fetal heart rate signal The fetal heart rate signal extraction algorithm will be based on the various signal processing tools developed by the INSERM CIC-IT 1403 laboratory at 15 minutes
Secondary The uterine contraction signal The uterine contraction signal extraction algorithm will be based on the different signal processing tools developed by the INSERM CIC-IT 1403 laboratory. at 15 minutes
Secondary Measuring the root mean square deviation between the heart rate signals from the device and the Doppler at 15 minutes
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