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NCT00811187 · ClinicalTrials.gov registry record · Phase 2
Paracervical Block During Office Hysteroscopy
A Phase 2 study, sponsored by Montefiore Medical Center.
- Completed
- Registry status
- Phase 2
- Development phase
- 80
- Enrollment target
NCT00811187 is a Phase 2 study that has completed, run by Montefiore Medical Center. The registered enrollment target is 80 participants.
The verdict
NCT00811187, a Phase 2 study, has completed, sponsored by Montefiore Medical Center.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 80 participants
- Enrollment target
Study 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.
Interventions
- DRUG Normal Saline
- DRUG Lidocaine paracervical block
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 80 participants |
| Start Date | 2007-03 |
| Est. Completion | 2008-09 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00811187
The ClinicalTrials.gov registry entry for NCT00811187 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Montefiore Medical Center, which has 345 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Normal Saline is the first listed.
NCT00811187 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00811187 about?
NCT00811187 is a clinical study titled "Paracervical Block During Office Hysteroscopy". 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 throug...
What is the current status of trial NCT00811187?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 80 participants. The study started on 2007-03. Estimated completion is 2008-09.
What interventions are being tested in trial NCT00811187?
The interventions under investigation include: Normal Saline (DRUG), Lidocaine paracervical block (DRUG).
Who is sponsoring clinical trial NCT00811187?
This trial is sponsored by Montefiore Medical Center, which has 345 total clinical trials registered on ClinicalTrials.gov.
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