Combined Ketorolac and Lidocaine Paracervical Block for Office Hysteroscopy: a Randomized Controlled Trial
Status: Recruiting
Location: See location...
Intervention Type: Procedure, Drug
Study Type: Interventional
Study Phase: Phase 1
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.
Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: t
View:
• Patients assigned female at birth,
• booked for office hysteroscopy at Mount Sinai Hospital faculty practice associates.
Locations
United States
New York
Mount Sinai
RECRUITING
New York
Contact Information
Primary
Kathleen E Ackert, DO
kathleen.ackert@mssm.edu
212-241-4500
Backup
Virginia H Flatow, MD
virginia.flatow@mssm.edu
Time Frame
Start Date: 2025-02-27
Estimated Completion Date: 2026-09-01
Participants
Target number of participants: 60
Treatments
Placebo_comparator: Lidocaine alone
Paracervical block will be performed with just lidocaine
Experimental: Lidocaine plus ketorolac
Paracervical block will be performed with lidocaine plus ketorolac
Related Therapeutic Areas
Sponsors
Leads: Icahn School of Medicine at Mount Sinai