RecruitingPhase 1NCT06653400

Combined Ketorolac and Lidocaine Paracervical Block for Office Hysteroscopy

Combined Ketorolac and Lidocaine Paracervical Block for Office Hysteroscopy: a Randomized Controlled Trial


Sponsor

Icahn School of Medicine at Mount Sinai

Enrollment

60 participants

Start Date

Feb 27, 2025

Study Type

INTERVENTIONAL

Conditions

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

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Lidocaine, a drug called ketorolac, and others for people with abnormal uterine bleeding, analgesia, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include women aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREparacervical block

paracervical block with office hysteroscopy

DRUGLidocaine

Dosage: 20 mL of 1% lidocaine

DRUGketorolac

Dosage: 2 mL (30 mg) of ketorolac


Locations(1)

Mount Sinai

New York, New York, United States

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NCT06653400


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