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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04397874
Other study ID # 003
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 1, 2019
Est. completion date September 1, 2025

Study information

Verified date March 2024
Source University of Campania "Luigi Vanvitelli"
Contact Marco La Verde, MD
Phone +393389412266
Email dr.marcolaverde@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Several studies analysed the association of fetal movement counting with perinatal mortality and fetal outcomes. However, no one examined the relationship of the maternal perception of fetal movement with the fetal wellbeing quantifies through computerised cardiotocography. Our study evaluates the correlation between the maternal perception of fetal movement and antepartum computerised cardiotocography parameters.


Recruitment information / eligibility

Status Recruiting
Enrollment 51
Est. completion date September 1, 2025
Est. primary completion date December 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 48 Years
Eligibility Inclusion Criteria: - nonlaboring term singleton pregnancies (37 0/7 - 41 6/7 weeks of gestation) Exclusion Criteria: - fetal malformations, stillbirths, preterm deliveries

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
; Computerized cardiotocography (cCTG)
To estimate the correlation between the maternal perception of fetal movement and antepartum computerised cardiotocography parameters.

Locations

Country Name City State
Italy Università degli studi della Campania "Luigi Vanvitelli"- OB & Gyn - Napoli Italia

Sponsors (1)

Lead Sponsor Collaborator
University of Campania "Luigi Vanvitelli"

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary To estimate the correlation between the maternal perception of fetal movement and antepartum computerised cardiotocography parameters. External cCTG was completed at least 20 minutes (maximum 60 minutes), two transducers were placed on the maternal abdomen: one over the fetal heart level and the other one at the uterine fundus. For each cCTG, the following data were evaluated: Basal FHR