Viewing Study NCT02196103


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Study NCT ID: NCT02196103
Status: UNKNOWN
Last Update Posted: 2014-07-21
First Post: 2014-07-15
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Management of Labor in Patients With Previous Cesarian Section
Sponsor: Hillel Yaffe Medical Center
Organization:

Study Overview

Official Title: Management of Labor in Patients With Previous Cesarian Section and Premature Rupture of Membranes Who Desire TOLAC: Comparison Between the Use of Standard Expectant Management and the Double-balloon Catheter Device. A Prospective Randomized Study
Status: UNKNOWN
Status Verified Date: 2014-07
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: None
Brief Summary: Induction of labor in women desiring TOLAC has long been a topic of controversy. The paucity of published data on mechanical cervical ripening in the setting of TOLAC and term PROM has led us to undertake the present clinical trial.
Detailed Description: None

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?: