Viewing Study NCT06591247



Ignite Creation Date: 2024-10-26 @ 3:40 PM
Last Modification Date: 2024-10-26 @ 3:40 PM
Study NCT ID: NCT06591247
Status: RECRUITING
Last Update Posted: None
First Post: 2024-08-07

Brief Title: Membrane Stripping for Cervical Ripening
Sponsor: None
Organization: None

Study Overview

Official Title: Evaluation of Stripping for Cervical Ripening - A Randomized Controlled Study
Status: RECRUITING
Status Verified Date: 2024-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: Stripping
Brief Summary: The goal of this interventional study is to evaluate the effectiveness of membrane stripping in cervical ripening compared to double balloon catheter induction

The study population consists of women undergoing labor induction

The main questions it aims to answer are

1 Is membrane stripping as effective as double balloon catheter induction in cervical ripening
2 What is the influence of membrane stripping on the time required for cervical ripening delivery duration and maternal and fetal outcomes compared to balloon induction
Detailed Description: None

Study Oversight

Has Oversight DMC: None
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?: None