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NCT01823224 · ClinicalTrials.gov registry record · NA
Comparing Effectiveness of IV vs Oral Acetaminophen Given Perioperatively for Lap Choles for Pain Control,
A NA study, sponsored by Defense and Veterans Center for Integrative Pain Management.
- Completed
- Registry status
- NA
- Development phase
- 67
- Enrollment target
NCT01823224 is a NA study that has completed, run by Defense and Veterans Center for Integrative Pain Management. The registered enrollment target is 67 participants.
The verdict
NCT01823224, a NA study, has completed, sponsored by Defense and Veterans Center for Integrative Pain Management.
- COMPLETED
- Registry status
- NA
- Development phase
- 67 participants
- Enrollment target
Study Summary
The purpose of the study is to learn whether perioperative IV (intravenous) administration of acetaminophen (commonly referred to as Tylenol) shows any different clinical outcomes over the oral (by mouth) administration of acetaminophen for a patient having a laparoscopic cholecystectomy. If improved pain scores occur with the administration of IV acetaminophen, it may result in fewer requests for pain-related intervention such as other oral pain medications.
Interventions
- DRUG 2 capsules Oral Tylenol 2000 mg and IV "salt water"
- DRUG IV tylenol 1000mg and 2 oral capsule "sugar pills"
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 67 participants |
| Start Date | 2013-02 |
| Est. Completion | 2015-09 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01823224
The ClinicalTrials.gov registry entry for NCT01823224 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 67 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Defense and Veterans Center for Integrative Pain Management, which has 19 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which 2 capsules Oral Tylenol 2000 mg and IV "salt water" is the first listed.
NCT01823224 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01823224 about?
NCT01823224 is a clinical study titled "Comparing Effectiveness of IV vs Oral Acetaminophen Given Perioperatively for Lap Choles for Pain Control,". The purpose of the study is to learn whether perioperative IV (intravenous) administration of acetaminophen (commonly referred to as Tylenol) shows any different clinical outcomes over the oral (by mouth) administration of acetaminophen for a patient having a laparoscopic cholecystectomy. If improve...
What is the current status of trial NCT01823224?
This trial is currently completed. It is a NA study. The enrollment target is 67 participants. The study started on 2013-02. Estimated completion is 2015-09.
What interventions are being tested in trial NCT01823224?
The interventions under investigation include: 2 capsules Oral Tylenol 2000 mg and IV "salt water" (DRUG), IV tylenol 1000mg and 2 oral capsule "sugar pills" (DRUG).
Who is sponsoring clinical trial NCT01823224?
This trial is sponsored by Defense and Veterans Center for Integrative Pain Management, which has 19 total clinical trials registered on ClinicalTrials.gov.
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