Viewing Study NCT07268118


Ignite Creation Date: 2025-12-25 @ 5:01 AM
Ignite Modification Date: 2025-12-26 @ 4:02 AM
Study NCT ID: NCT07268118
Status: NOT_YET_RECRUITING
Last Update Posted: 2025-12-05
First Post: 2025-11-24
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Pain Control for Cervical Ripening Balloon
Sponsor: Beth Israel Deaconess Medical Center
Organization:

Study Overview

Official Title: Randomized Control Trial for Pain Control With Topical Lidocaine for Cervical Ripening Balloon Placement
Status: NOT_YET_RECRUITING
Status Verified Date: 2025-12
Last Known Status: None
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: No standard of care exists for pain management during cervical ripening balloon placement. The purpose of this study is to evaluate if vaginal topical lidocaine reduces pain related to cervical ripening balloon placement during induction of labor.
Detailed Description: None

Study Oversight

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