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NCT01693588 · ClinicalTrials.gov registry record · NA
Study of a Multimodality Pain Management Protocol on Postoperative Neurosurgical Pain
A NA study of Pain and Postoperative Pain, sponsored by University of Florida.
- Completed
- Registry status
- NA
- Development phase
- 94
- Enrollment target
- 1
- Study location
NCT01693588 is a NA study of Pain and Postoperative Pain that has completed, run by University of Florida. The registered enrollment target is 94 participants, below the 304-participant average among 374 other Pain trials with a reported enrollment target (69% lower). The trial reports 1 study location across 1 state.
The verdict
NCT01693588, a NA study of Pain and Postoperative Pain, has completed, sponsored by University of Florida.
- COMPLETED
- Registry status
- NA
- Development phase
- 94 participants
- Enrollment target
- 1
- Study location
Study Summary
High levels of postoperative pain are associated with an increased risk of lung and heart complications, are the most common reason for delayed discharge or for unexpected hospital admission after ambulatory surgery, and are responsible for prolonged recovery after inpatient surgery. Furthermore both neuropathic pain and post surgical pain inhibit weight gain and may have an impact on the patient's nutrition post operatively. The purpose of this study is to evaluate the effectiveness of a multimodality pain management protocol on postoperative neurosurgical pain.
Conditions Studied
Interventions
- OTHER Pain Management Bundle
Study Locations (1)
Florida
- University of Florida - Gainesville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 94 participants |
| Start Date | 2012-10 |
| Est. Completion | 2013-08 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01693588
The ClinicalTrials.gov registry entry for NCT01693588 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 94 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 (69% lower). The listed sponsor is University of Florida, which has 1,106 total studies on file at ClinicalTrials.gov.
The record links to 4 conditions, with Pain appearing as the primary indexed condition, and to 1 intervention - of which Pain Management Bundle is the first listed.
NCT01693588 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.
Frequently Asked Questions
What is clinical trial NCT01693588 about?
NCT01693588 is a clinical study titled "Study of a Multimodality Pain Management Protocol on Postoperative Neurosurgical Pain". High levels of postoperative pain are associated with an increased risk of lung and heart complications, are the most common reason for delayed discharge or for unexpected hospital admission after ambulatory surgery, and are responsible for prolonged recovery after inpatient surgery. Furthermore bot...
What is the current status of trial NCT01693588?
This trial is currently completed. It is a NA study. The enrollment target is 94 participants. The study started on 2012-10. Estimated completion is 2013-08.
What conditions does trial NCT01693588 study?
This clinical trial studies the following conditions: Pain, Postoperative Pain, Surgical Pain, Neurosurgical Pain.
What interventions are being tested in trial NCT01693588?
The interventions under investigation include: Pain Management Bundle (OTHER).
Who is sponsoring clinical trial NCT01693588?
This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01693588 being conducted?
This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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