Paracervical Block During Office Hysteroscopy

Completed · Phase 2 · Has a placebo group

Conditions studied: Paracervical Block

In brief

The purpose of this study is to determine the effectiveness of paracervical block for pain relief in office hysteroscopy - particularly with the placement of the Essure device. Subjects will be randomized to receive either paracervical block or saline, and will have pain assessments performed throughout the procedure. Subjects and physicians will be blinded to group assignments.

Key facts

Study ID

NCT00811187

Run by

Montefiore Medical Center

People needed

80

Starts

2007-03-01

Expected to finish

2008-09-01

Last updated by the study team

2019-12-11

Who can join

Age: 21 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Women eligible and scheduled for office hysteroscopic placement of essure devices

You may not qualify if…

• Planned secondary procedures
• Lidocaine allergy
• Repeat procedures

Where it is running

• Centennial Women's Center / Montefiore Medical Center — The Bronx, New York, United States

Full record on ClinicalTrials.gov

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