DilaCheck Cervical Dilation Measurement Trial

Status Completed

Clinical Trial Summary

Trial to compare the interexaminer agreement between two cervical dilation examinations conducted by Labor and Delivery physicians when using standard methods versus DilaCheck device.

Clinical Trial Description

The trial seeks to compare the DilaCheck device with standard digital cervical dilation examinations. 50 laboring female participants will be enrolled with 25 randomly assigned to the control arm and 25 to the treatment (DilaCheck) arm. Each participant will receive two cervical dilation examinations from two separate physicians. The main outcome measure is agreement between the two cervical dilation measurements. Secondary outcomes include ease of use of the device and pain levels. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03440723
Study type	Interventional
Source	Elm Tree Medical Inc.
Contact
Status	Completed
Phase	N/A
Start date	January 6, 2020
Completion date	March 30, 2020

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