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NCT02881996 · ClinicalTrials.gov registry record · NA
The Impact of IV Acetaminophen on Pain After Appendectomy for Perforated Appendicitis
A NA study, sponsored by Children's Mercy Hospital Kansas City.
- Completed
- Registry status
- NA
- Development phase
- 90
- Enrollment target
NCT02881996 is a NA study that has completed, run by Children's Mercy Hospital Kansas City. The registered enrollment target is 90 participants.
The verdict
NCT02881996, a NA study, has completed, sponsored by Children's Mercy Hospital Kansas City.
- COMPLETED
- Registry status
- NA
- Development phase
- 90 participants
- Enrollment target
Study Summary
The objective of this study is to evaluate two standard post-operative pain regimens routinely used after laparoscopic appendectomy for perforated appendicitis. The investigators hypothesize that the use of intravenous (IV) acetaminophen in addition to IV ketorolac with narcotic pain pump will decrease time to transition off patient/nurse controlled analgesia (PCA) to oral pain medications.
Interventions
- DRUG Ketorolac
- DRUG IV tylenol
- DRUG No IV tylenol
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 90 participants |
| Start Date | 2014-06 |
| Est. Completion | 2016-08 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02881996
The ClinicalTrials.gov registry entry for NCT02881996 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 90 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Children's Mercy Hospital Kansas City, which has 184 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which Ketorolac is the first listed.
NCT02881996 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02881996 about?
NCT02881996 is a clinical study titled "The Impact of IV Acetaminophen on Pain After Appendectomy for Perforated Appendicitis". The objective of this study is to evaluate two standard post-operative pain regimens routinely used after laparoscopic appendectomy for perforated appendicitis. The investigators hypothesize that the use of intravenous (IV) acetaminophen in addition to IV ketorolac with narcotic pain pump will decre...
What is the current status of trial NCT02881996?
This trial is currently completed. It is a NA study. The enrollment target is 90 participants. The study started on 2014-06. Estimated completion is 2016-08.
What interventions are being tested in trial NCT02881996?
The interventions under investigation include: Ketorolac (DRUG), IV tylenol (DRUG), No IV tylenol (DRUG).
Who is sponsoring clinical trial NCT02881996?
This trial is sponsored by Children's Mercy Hospital Kansas City, which has 184 total clinical trials registered on ClinicalTrials.gov.
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