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NCT00318292 · ClinicalTrials.gov registry record · Phase 4
Preemptive Local Anesthesia in Vaginal Surgery
A Phase 4 study of Pain, Postoperative, sponsored by Mayo Clinic.
- Completed
- Registry status
- Phase 4
- Development phase
- 90
- Enrollment target
- 1
- Study location
NCT00318292 is a Phase 4 study of Pain, Postoperative that has completed, run by Mayo Clinic. The registered enrollment target is 90 participants, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (67% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00318292, a Phase 4 study of Pain, Postoperative, has completed, sponsored by Mayo Clinic.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 90 participants
- Enrollment target
- 1
- Study location
Study Summary
Preemptive analgesia is an intervention which provides an anesthetic prior to initiating a painful stimulus. This trial is examining the effects of a local anesthetic given at the point of innervation prior to performing a vaginal hysterectomy with suspension sutures.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG bupivacaine and epinephrine
Study Locations (1)
Arizona
- Mayo Clinic - Scottsdale
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 90 participants |
| Start Date | 2006-04 |
| Est. Completion | 2008-03 |
| Phase | Phase 4 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00318292
The ClinicalTrials.gov registry entry for NCT00318292 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 90 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (67% lower). The listed sponsor is Mayo Clinic, which has 2,844 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Pain, Postoperative appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.
NCT00318292 reports 1 study location spanning 1 distinct geographic area - top geographies include Arizona.
Frequently Asked Questions
What is clinical trial NCT00318292 about?
NCT00318292 is a clinical study titled "Preemptive Local Anesthesia in Vaginal Surgery". Preemptive analgesia is an intervention which provides an anesthetic prior to initiating a painful stimulus. This trial is examining the effects of a local anesthetic given at the point of innervation prior to performing a vaginal hysterectomy with suspension sutures.
What is the current status of trial NCT00318292?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 90 participants. The study started on 2006-04. Estimated completion is 2008-03.
What conditions does trial NCT00318292 study?
This clinical trial studies the following conditions: Pain, Postoperative.
What interventions are being tested in trial NCT00318292?
The interventions under investigation include: Placebo (DRUG), bupivacaine and epinephrine (DRUG).
Who is sponsoring clinical trial NCT00318292?
This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00318292 being conducted?
This trial has 1 study location across Arizona. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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