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NCT01783236 · ClinicalTrials.gov registry record · Phase 4
Analgesic Efficacy of Intravenous Acetaminophen After Video-assisted Thoracic Surgery
A Phase 4 study of Lung Tumor, sponsored by Weill Medical College of Cornell University.
- Completed
- Registry status
- Phase 4
- Development phase
- 16
- Enrollment target
- 1
- Study location
NCT01783236: Completed Phase 4 study of Lung Tumor, sponsored by Weill Medical College of Cornell University.
NCT01783236 is a Phase 4 study of Lung Tumor that has completed, run by Weill Medical College of Cornell University. The registered enrollment target is 16 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01783236, a Phase 4 study of Lung Tumor, has completed, sponsored by Weill Medical College of Cornell University.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 16 participants
- Enrollment target
- 1
- Study location
Study Summary
We will study the efficacy of FDA approved intravenous (IV) acetaminophen ("Ofirmev", © 2011 Cadence Pharmaceuticals, Inc.) in reducing opioid consumption after minimally invasive thoracic surgery in a double blind randomized trial. This drug has been shown in Europe to reduce the need for patient controlled analgesia and the total dose of opioids, which have serious side effects in thoracic surgery patients. We will compare the use of IV patient-controlled morphine (PCA) in two groups of subjects in treating postoperative pain. We will determine if IV acetaminophen reduces post-operative morphine requirements (primary end point). We will also assess subject pain scores and post-operative complications associated with pain management as secondary end points. Our hypothesis is that the study arm receiving intravenous acetaminophen will have lower total morphine consumptions compared to the placebo group.
Primary Outcome
How much morphine the subject consumes in the first 24 hours after surgery (mg).
Conditions Studied
Interventions
- DRUG Saline Placebo
- DRUG IV Acetaminophen
Study Locations (1)
New York
- Weill Cornell Medical College - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 16 participants |
| Start Date | 2013-06 |
| Est. Completion | 2015-07 |
| Phase | Phase 4 |
What the finished NCT01783236 record still lists
NCT01783236 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 16 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (97% lower).
The record links to 1 condition, with Lung Tumor appearing as the primary indexed condition, and to 2 interventions - of which Saline Placebo is the first listed.
NCT01783236 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT01783236 about?
NCT01783236 is a clinical study titled "Analgesic Efficacy of Intravenous Acetaminophen After Video-assisted Thoracic Surgery". We will study the efficacy of FDA approved intravenous (IV) acetaminophen ("Ofirmev", © 2011 Cadence Pharmaceuticals, Inc.) in reducing opioid consumption after minimally invasive thoracic surgery in a double blind randomized trial. This drug has been shown in Europe to reduce the need for patient c...
What is the current status of trial NCT01783236?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 16 participants. The study started on 2013-06. Estimated completion is 2015-07.
What conditions does trial NCT01783236 study?
This clinical trial studies the following conditions: Lung Tumor.
What interventions are being tested in trial NCT01783236?
The interventions under investigation include: Saline Placebo (DRUG), IV Acetaminophen (DRUG).
Who is sponsoring clinical trial NCT01783236?
This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01783236 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT01783236's enrollment target sits among peer trials
16 1870th of 2000 higher than 121 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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