Viewing Study NCT02283606


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Study NCT ID: NCT02283606
Status: UNKNOWN
Last Update Posted: 2015-09-23
First Post: 2014-10-26
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: Sonoelastography of the Uterine Cervix Before Induction of Labor
Sponsor: Meir Medical Center
Organization:

Study Overview

Official Title: Sonoelastography of the Uterine Cervix Before Induction of Labor
Status: UNKNOWN
Status Verified Date: 2015-09
Last Known Status: NOT_YET_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: SUCI
Brief Summary: The investigators aim to measure sonoelastographically the elasticity of the uterine cervix in pregnant patients at term before induction of labor and compare between patients with successful and failed inductions.
Detailed Description: Softening of the uterine cervix in pregnant patients at term causes changes in its elasticity.these changes may affect success or failure in induction of labor.The elasticity of the uterine cervix is usually evaluated clinically and subjectively by vaginal examination (bishop's score) which is not very predictive.We aim to measure the elasticity quantitatively and objectively.The difference in strain, in the area of the internal os , is often illustrated by a color map, where low stiffness (soft tissue) is indicated in red, middle stiffness is in green and high stiffness (hard tissue) is in blue.The color maps will be compared between patients with successful and failed inductions.

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: