Trials / Completed
CompletedNCT00811187
Paracervical Block During Office Hysteroscopy
Paracervical Block During Office Hysteroscopy: A Randomized Double Blind Placebo-controlled Trial
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 80 (actual)
- Sponsor
- Montefiore Medical Center · Academic / Other
- Sex
- Female
- Age
- 21 Years
- Healthy volunteers
- Accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Lidocaine paracervical block | 5cc 1% lidocaine injection in each paracervical region |
| DRUG | Normal Saline | 5cc Normal Saline injection in each paracervical region |
Timeline
- Start date
- 2007-03-01
- Primary completion
- 2008-03-01
- Completion
- 2008-09-01
- First posted
- 2008-12-18
- Last updated
- 2019-12-11
- Results posted
- 2019-12-11
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT00811187. Inclusion in this directory is not an endorsement.