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NCT03365622 · ClinicalTrials.gov registry record · Phase 4

Efficacy of IV Acetaminophen Versus Oral Acetaminophen

A Phase 4 study, sponsored by University of Rochester.

Completed
Registry status
Phase 4
Development phase
214
Enrollment target

NCT03365622 is a Phase 4 study that has completed, run by University of Rochester. The registered enrollment target is 214 participants.

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The verdict

NCT03365622, a Phase 4 study, has completed, sponsored by University of Rochester.

COMPLETED
Registry status
Phase 4
Development phase
214 participants
Enrollment target

Study Summary

The aim of this study is to determine whether intravenous acetaminophen compared to enteric acetaminophen offers increased efficacy in patients who are scheduled for laparoscopic donor nephrectomy and for patients scheduled for robot-assisted, laparoscopic nephrectomy for cancer at the University of Rochester Medical Center. The standard surgical and post-operative care, including post-operative pain management will not be altered.

Interventions

  • DRUG Acetaminophen
  • DRUG Placebos
  • DRUG Placebo Oral Tablet
  • DRUG acetaminophen

Trial Details

FieldValue
Enrollment Target 214 participants
Start Date 2018-08-08
Est. Completion 2024-04-10
Phase Phase 4

Sponsor

University of Rochester

636 total trials

What the Registry Record Tells You About NCT03365622

The ClinicalTrials.gov registry entry for NCT03365622 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 214 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Rochester, which has 636 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 4 interventions - of which Acetaminophen is the first listed.

NCT03365622 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03365622 about?

NCT03365622 is a clinical study titled "Efficacy of IV Acetaminophen Versus Oral Acetaminophen". The aim of this study is to determine whether intravenous acetaminophen compared to enteric acetaminophen offers increased efficacy in patients who are scheduled for laparoscopic donor nephrectomy and for patients scheduled for robot-assisted, laparoscopic nephrectomy for cancer at the University of...

What is the current status of trial NCT03365622?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 214 participants. The study started on 2018-08-08. Estimated completion is 2024-04-10.

What interventions are being tested in trial NCT03365622?

The interventions under investigation include: Acetaminophen (DRUG), Placebos (DRUG), Placebo Oral Tablet (DRUG), acetaminophen (DRUG).

Who is sponsoring clinical trial NCT03365622?

This trial is sponsored by University of Rochester, which has 636 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.