Paracervical Block for Pain Reduction in Saline Infusion Sonograms

Recruiting Phase 4 Interventional Study
Pain During Saline Infusion Sonogram
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 – 50
Sex
Female
Trial phase
Phase 4
Study type
Interventional
Purpose
Supportive Care
Participants needed
246 (estimated)
Sponsor
Montefiore Medical Center · Other
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial
Inadequate pain management during gynecologic procedures is a growing women's health concern, especially as it reduces access to care for patients who may subsequently avoid further treatment. Although recent evidence has shown that local anesthesia reduces pain during certain gynecologic procedures, such as intrauterine (IUD) placements, there is still limited evidence on the effectiveness of loc…
Trial Locations
Loading…

Loading trial locations…

Eligibility Criteria
Inclusion Criteria: * Undergoing uterine cavity and tubal patency evaluation via saline infusion sonogram with balloon catheter at Montefiore Institute for Reproductive Medicine and Health * Pre-medicated with 600-800 mg ibuprofen taken 30 minutes to 4 hours prior to procedure * Able to provide inf…
Contacts

Meaghan Jain, MD

781-439-5947

mejain@montefiore.org

CONTACT

Julian Gingold, MD, PhD

914-997-1060

jgingold@montefiore.org

CONTACT