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NCT00816751 · ClinicalTrials.gov registry record · NA
Paracervical Versus Intracervical Lidocaine
A NA study, sponsored by University of California, San Diego.
- Completed
- Registry status
- NA
- Development phase
- 89
- Enrollment target
NCT00816751 is a NA study that has completed, run by University of California, San Diego. The registered enrollment target is 89 participants.
The verdict
NCT00816751, a NA study, has completed, sponsored by University of California, San Diego.
- COMPLETED
- Registry status
- NA
- Development phase
- 89 participants
- Enrollment target
Study Summary
The aim of this study is to estimate the efficacy of intracervical versus paracervical block on pain experienced during first trimester suction curettage without the use of preoperative cervical ripening. Because of the theoretical improved reliability of stromal block, the investigators hypothesize that intracervical block would produce lower pain scores than paracervical block at the time of cervical dilation.
Interventions
- PROCEDURE Paracervical block
- PROCEDURE Intracervical
- DRUG Buffered Lidocaine, vasopressin, sodium bicarbonate
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 89 participants |
| Start Date | 2007-12 |
| Est. Completion | 2008-02 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00816751
The ClinicalTrials.gov registry entry for NCT00816751 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 89 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, San Diego, which has 775 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which Paracervical block is the first listed.
NCT00816751 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00816751 about?
NCT00816751 is a clinical study titled "Paracervical Versus Intracervical Lidocaine". The aim of this study is to estimate the efficacy of intracervical versus paracervical block on pain experienced during first trimester suction curettage without the use of preoperative cervical ripening. Because of the theoretical improved reliability of stromal block, the investigators hypothesize...
What is the current status of trial NCT00816751?
This trial is currently completed. It is a NA study. The enrollment target is 89 participants. The study started on 2007-12. Estimated completion is 2008-02.
What interventions are being tested in trial NCT00816751?
The interventions under investigation include: Paracervical block (PROCEDURE), Intracervical (PROCEDURE), Buffered Lidocaine, vasopressin, sodium bicarbonate (DRUG).
Who is sponsoring clinical trial NCT00816751?
This trial is sponsored by University of California, San Diego, which has 775 total clinical trials registered on ClinicalTrials.gov.
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