Paracervical Block During Office Hysteroscopy

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Clinical Trial Summary

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.

See also
	Status	Clinical Trial	Phase
	Completed	`NCT01534416` - Effect of Paracervical Block on Post Operative Pain in Laparoscopic Gynecologic Surgery	N/A
	Completed	`NCT01947205` - Pain and Suction Curettage	N/A

NCT number	NCT00811187
Study type	Interventional
Source	Montefiore Medical Center
Contact
Status	Completed
Phase	Phase 2
Start date	March 2007
Completion date	September 2008

Paracervical Block During Office Hysteroscopy

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms