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NCT02025634 · ClinicalTrials.gov registry record · Phase 4
Intravenous Acetaminophen for Non-Narcotic Postoperative Pain Management Following Knee Arthroscopy
A Phase 4 study, sponsored by AdventHealth.
- Completed
- Registry status
- Phase 4
- Development phase
- 119
- Enrollment target
NCT02025634: Completed Phase 4 study, sponsored by AdventHealth.
NCT02025634 is a Phase 4 study that has completed, run by AdventHealth. The registered enrollment target is 119 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02025634, a Phase 4 study, has completed, sponsored by AdventHealth.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 119 participants
- Enrollment target
Study Summary
The purpose of this randomized, placebo controlled, single blind study is to determine if postoperative pain levels, as measured by a verbal numeric pain rating scale (VNRS), are reduced with the administration of IV acetaminophen when compared to a control group. Particular focus will be on the postoperative opioid consumption. In addition, we will ascertain if the total time the participant is in the PACU differs in those who receive the IV acetaminophen versus those who do not.
Primary Outcome
To determine if postoperative pain levels, as measured by a Verbal Numerical Rating Scale (VNRS), are reduced with the administration of IV acetaminophen when compared to a control group. In the VNRS, the user has the option to verbally rate their scale from 0 to 10. Zero indicates the absence of pain, while 10 represents the most intense pain possible.
Interventions
- DRUG Intravenous Acetaminophen
- DRUG Placebo (0.9% Normal Saline infusion)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 119 participants |
| Start Date | 2013-11 |
| Est. Completion | 2015-07 |
| Phase | Phase 4 |
What the finished NCT02025634 record still lists
NCT02025634 is an interventional study that assigns participants to a tested intervention. The registered 119 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (77% lower).
The record links to 0 conditions, and to 2 interventions - of which Intravenous Acetaminophen is the first listed.
NCT02025634 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02025634 about?
NCT02025634 is a clinical study titled "Intravenous Acetaminophen for Non-Narcotic Postoperative Pain Management Following Knee Arthroscopy". The purpose of this randomized, placebo controlled, single blind study is to determine if postoperative pain levels, as measured by a verbal numeric pain rating scale (VNRS), are reduced with the administration of IV acetaminophen when compared to a control group. Particular focus will be on the pos...
What is the current status of trial NCT02025634?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 119 participants. The study started on 2013-11. Estimated completion is 2015-07.
What interventions are being tested in trial NCT02025634?
The interventions under investigation include: Intravenous Acetaminophen (DRUG), Placebo (0.9% Normal Saline infusion) (DRUG).
Who is sponsoring clinical trial NCT02025634?
This trial is sponsored by AdventHealth, which has 95 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02025634's enrollment target sits among peer trials
119 712th of 2000 higher than 1,288 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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