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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02870608
Other study ID # API/2015/60
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 2016
Est. completion date March 14, 2017

Study information

Verified date January 2018
Source Centre Hospitalier Universitaire de Besancon
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of the study was to evaluated the feasibility and reproducibility of the measurement of lung elasticity report / fetal liver according to gestational age in a group of patients with a normal course of pregnancy and in a group of Patients at risk of preterm delivery.


Recruitment information / eligibility

Status Completed
Enrollment 103
Est. completion date March 14, 2017
Est. primary completion date November 14, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria for control group :

- major pregnant women

- singleton pregnancy

Inclusion Criteria for control group :

- major pregnant women

- singleton pregnancy

- hospitalized for threatened premature birth between 24 and 34 WA

- Indication of a cure corticosteroid betamethasone

Exclusion Criteria:

- maternal conditions of pregnancy: diabetes gestational, pregnancy-induced hypertension, preeclampsia

- fetal lung diseases

Study Design


Intervention

Other:
lung and liver elastography measurement of fetus


Locations

Country Name City State
France CHU de Besançon Besançon

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Besancon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evolution over 48 hours of the fetal lung elasticity coefficient measure in kilopascals (kPa) (compared to the fetal liver) The dates of elastography exams controls patients will be distributed a week of amenorrhea (WA) between 24 and 34 WA. For pretern larbor group: day of hospitalization for preterm labor, then 2 days later. For control group, both measurements at 2-day intervals
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