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NCT01466491 · ClinicalTrials.gov registry record · Phase 4
Refining Paracervical Block Techniques for Pain Control in First Trimester Surgical Abortion
A Phase 4 study, sponsored by Oregon Health and Science University.
- Completed
- Registry status
- Phase 4
- Development phase
- 332
- Enrollment target
NCT01466491 is a Phase 4 study that has completed, run by Oregon Health and Science University. The registered enrollment target is 332 participants.
The verdict
NCT01466491, a Phase 4 study, has completed, sponsored by Oregon Health and Science University.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 332 participants
- Enrollment target
Study Summary
The purpose of this study is to determine the level of pain women experience with a surgical abortion and the effect that varying paracervical block techniques might have on that pain. These different techniques involve wait time following the injection as well as the number of sites injected.
Interventions
- DRUG Paracervical block technique with lidocaine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 332 participants |
| Start Date | 2011-10 |
| Est. Completion | 2013-05 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01466491
The ClinicalTrials.gov registry entry for NCT01466491 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 332 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Oregon Health and Science University, which has 546 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Paracervical block technique with lidocaine is the first listed.
NCT01466491 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01466491 about?
NCT01466491 is a clinical study titled "Refining Paracervical Block Techniques for Pain Control in First Trimester Surgical Abortion". The purpose of this study is to determine the level of pain women experience with a surgical abortion and the effect that varying paracervical block techniques might have on that pain. These different techniques involve wait time following the injection as well as the number of sites injected.
What is the current status of trial NCT01466491?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 332 participants. The study started on 2011-10. Estimated completion is 2013-05.
What interventions are being tested in trial NCT01466491?
The interventions under investigation include: Paracervical block technique with lidocaine (DRUG).
Who is sponsoring clinical trial NCT01466491?
This trial is sponsored by Oregon Health and Science University, which has 546 total clinical trials registered on ClinicalTrials.gov.
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