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NCT01126359 · ClinicalTrials.gov registry record · NA
Lidocaine Analgesia For Removal Of Wound Vac Dressings
A NA study of Pain, sponsored by University of Utah.
- Completed
- Registry status
- NA
- Development phase
- 11
- Enrollment target
- 1
- Study location
NCT01126359 is a NA study of Pain that has completed, run by University of Utah. The registered enrollment target is 11 participants, below the 304-participant average among 374 other Pain trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state.
The verdict
NCT01126359, a NA study of Pain, has completed, sponsored by University of Utah.
- COMPLETED
- Registry status
- NA
- Development phase
- 11 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this prospective study is to compare pain levels and pain medication dose requirements in patients with topical negative pressure (TNP) dressings removed in a standard manner (i.v. or p.o. pain meds) compared to dressings removed with lidocaine analgesia, via injection retrograde up the suction tube into the foam prior to removal. Our null hypothesis is that there will be no difference in overall pain scores or medication requirements when patients receive a saline, control injection and pain medications, compared to when their dressings are changed with a lidocaine injection into the sponge, with pain medications. Our objective is to disprove this null hypothesis with statistical significance.
Conditions Studied
Interventions
- DRUG Lidocaine
- DRUG Placebo-Saline
Study Locations (1)
Utah
- University of Utah - Salt Lake City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 11 participants |
| Start Date | 2008-08 |
| Est. Completion | 2010-03 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01126359
The ClinicalTrials.gov registry entry for NCT01126359 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 11 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 304-participant average among 374 other Pain trials with a reported enrollment target (96% lower). The listed sponsor is University of Utah, which has 818 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Pain appearing as the primary indexed condition, and to 2 interventions - of which Lidocaine is the first listed.
NCT01126359 reports 1 study location spanning 1 distinct geographic area - top geographies include Utah.
Frequently Asked Questions
What is clinical trial NCT01126359 about?
NCT01126359 is a clinical study titled "Lidocaine Analgesia For Removal Of Wound Vac Dressings". The purpose of this prospective study is to compare pain levels and pain medication dose requirements in patients with topical negative pressure (TNP) dressings removed in a standard manner (i.v. or p.o. pain meds) compared to dressings removed with lidocaine analgesia, via injection retrograde up t...
What is the current status of trial NCT01126359?
This trial is currently completed. It is a NA study. The enrollment target is 11 participants. The study started on 2008-08. Estimated completion is 2010-03.
What conditions does trial NCT01126359 study?
This clinical trial studies the following conditions: Pain.
What interventions are being tested in trial NCT01126359?
The interventions under investigation include: Lidocaine (DRUG), Placebo-Saline (DRUG).
Who is sponsoring clinical trial NCT01126359?
This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01126359 being conducted?
This trial has 1 study location across Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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