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NCT03391284 · ClinicalTrials.gov registry record · NA

Oral vs Intravenous Acetominophen for Postoperative Pain in Minimally Invasive Gynecologic Surgery

A NA study of Post Operative Pain, sponsored by Scripps Health.

Completed
Registry status
NA
Development phase
75
Enrollment target
2
Study locations

NCT03391284 is a NA study of Post Operative Pain that has completed, run by Scripps Health. The registered enrollment target is 75 participants, below the 235-participant average among 56 other Post Operative Pain trials with a reported enrollment target (68% lower). The trial reports 2 study locations across 1 state.

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The verdict

NCT03391284, a NA study of Post Operative Pain, has completed, sponsored by Scripps Health.

COMPLETED
Registry status
NA
Development phase
75 participants
Enrollment target
2
Study locations

Study Summary

Hypothesis: Postoperative pain will be equivalent in patients receiving preemptive oral acetaminophen as compared to patients receiving preemptive intravenous acetaminophen following minimally invasive benign gynecologic surgery. Primary outcome: • Difference in postoperative pain comparing preemptive use of PO versus IV acetaminophen o Mean Visual analog Scale (VAS) scores will be compared between the intervention group (PO acetaminophen) and the control group (IV acetaminophen). Secondary outcomes: * Difference in postoperative analgesic use between groups o Narcotics, NSAIDs * Difference in postoperative N/V between groups o Patient rated measure - none, mild, moderate, severe * Cost comparison between drugs

Conditions Studied

Post Operative Pain

Interventions

  • DRUG Acetaminophen
  • DRUG acetominophen

Study Locations (2)

California

  • Scripps Clinic - San Diego
  • Scripps Clininc Dept of Ob/Gyn - San Diego

Trial Details

FieldValue
Enrollment Target 75 participants
Start Date 2016-02
Est. Completion 2018-02
Phase NA

Sponsor

Scripps Health

30 total trials

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What the Registry Record Tells You About NCT03391284

The ClinicalTrials.gov registry entry for NCT03391284 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 75 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 235-participant average among 56 other Post Operative Pain trials with a reported enrollment target (68% lower). The listed sponsor is Scripps Health, which has 30 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Post Operative Pain appearing as the primary indexed condition, and to 2 interventions - of which Acetaminophen is the first listed.

NCT03391284 reports 2 study locations spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT03391284 about?

NCT03391284 is a clinical study titled "Oral vs Intravenous Acetominophen for Postoperative Pain in Minimally Invasive Gynecologic Surgery". Hypothesis: Postoperative pain will be equivalent in patients receiving preemptive oral acetaminophen as compared to patients receiving preemptive intravenous acetaminophen following minimally invasive benign gynecologic surgery. Primary outcome: • Difference in postoperative pain comparing preemp...

What is the current status of trial NCT03391284?

This trial is currently completed. It is a NA study. The enrollment target is 75 participants. The study started on 2016-02. Estimated completion is 2018-02.

What conditions does trial NCT03391284 study?

This clinical trial studies the following conditions: Post Operative Pain.

What interventions are being tested in trial NCT03391284?

The interventions under investigation include: Acetaminophen (DRUG), acetominophen (DRUG).

Who is sponsoring clinical trial NCT03391284?

This trial is sponsored by Scripps Health, which has 30 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03391284 being conducted?

This trial has 2 study locations across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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.