Ignite Creation Date:
2024-10-25 @ 8:06 PM
Last Modification Date:
2024-10-26 @ 3:43 PM
Study NCT ID:
NCT06653400
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-10-20
Brief Title:
Combined Ketorolac and Lidocaine Paracervical Block for Office Hysteroscopy
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Combined Ketorolac and Lidocaine Paracervical Block for Office Hysteroscopy a Randomized Controlled Trial
Status:
RECRUITING
Status Verified Date:
2024-10
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:
None
Brief Summary:
A randomized double-blind placebo controlled trial comparing the effect of a combined ketorolac and lidocaine paracervical block with a standard lidocaine paracervical block on procedure related pain with office hysteroscopies
Detailed Description:
A randomized double-blind placebo controlled trial comparing the effect of a combined ketorolac and lidocaine paracervical block with a standard lidocaine paracervical block on procedure related pain with office hysteroscopies Primary Objective To study the effect of a combined ketorolac and lidocaine paracervical block on procedure related pain with office hysteroscopy Secondary Objectives To study the effect of a combined ketorolac and lidocaine paracervical block on patient satisfaction and post procedure pain To assess for major adverse events with the use of a combined ketorolac and lidocaine paracervical block for office hysteroscopy when compared with a standard lidocaine paracervical block Primary Endpoint Pain on a 100 mm visual analogue scale during cervical dilation Secondary Endpoints Pain on a 100 mm visual analogue scale during the paracervical block during the office hysteroscopy immediately after the hysteroscopy and 30 minutes after the procedure Other secondary endpoints include patient satisfaction frequency of procedure termination and adverse events Patients assigned female at birth booked for office hysteroscopy at Mount Sinai Hospital faculty practice associates Patients scheduled for office hysteroscopy through seeing a Gynecologist at either 5 E 98th Street Faculty Practice Associates or 1176 5th Avenue Gynecology Practice 5 E 98th Street primarily cares for privately insured patients while 1176 5th Avenue cares for a mix of privately insured as well as patients insured with Medicaid Regardless of recruitment site all office hysteroscopies will be performed at the 5 E 98th Street facility A randomized controlled trial designed to investigate if ketorolac added to a paracervical block reduces procedure related pain Patient will be randomized to a standard paracervical block versus a paracervical block with ketorolac added The study will be conducted over two years Patients will be followed for the duration of the two-year study period
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