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NCT01912508 Clinical Trial

Preterm Labor Prediction by Cervical Contour in Ultrasound

Preterm Labor Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01912508
Other study ID # MMC-12-0152CTIL
Secondary ID
Status Recruiting
Phase N/A
First received July 29, 2013
Last updated August 12, 2014
Start date August 2013

Study information
Verified date August 2014
Source Meir Medical Center
Contact Efrat Hadi, Dr
Phone 09-7472871/2
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

Cervical length is a already known predictor for preterm labor. In this study the investigators want to examining the hypothesis that cervical curvature is also a predictor for preterm labor and that moderate transducer pressure influence cervical length.

study population: 200 consecutive pregnant women between 14-34w, visiting in the ultrasound unit ether for routine screening or because of preterm labor.

During their examination cervical length and curvature measurements will be taken. Another measurement will be taken after applying moderate cervical pressure.

The investigators will compere cervical contour and pressure influence between groups and according to cervical length Demographic data will be taken at the time of recruitment and pregnancy outcome measures in a later telephone interview.

Recruitment information / eligibility
Status Recruiting
Enrollment 200
Est. completion date
Est. primary completion date August 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria:

- pregnancy

Exclusion Criteria:

- cervical cerclage

- pre term rupture on membrane in current pregnancy

- unknown dating of pregnancy

Study Design

Observational Model: Case Control

Related Conditions & MeSH terms

Locations
Country Name City State
Israel Meir hospital Kfar Saba

Sponsors (1)
Lead Sponsor Collaborator
Meir Medical Center

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary cervical curvature 12 months No
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