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NCT05548582 · ClinicalTrials.gov registry record · NA

Reduced Opioid Prescription After Laparoscopic Hysterectomy

A NA study of Pain and Pain, Postoperative, sponsored by Johns Hopkins University.

Active
Registry status
NA
Development phase
120
Enrollment target
1
Study location

NCT05548582 is a NA study of Pain and Pain, Postoperative that is active but no longer recruiting, run by Johns Hopkins University. The registered enrollment target is 120 participants, below the 304-participant average among 374 other Pain trials with a reported enrollment target (61% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05548582, a NA study of Pain and Pain, Postoperative, is active but no longer recruiting, sponsored by Johns Hopkins University.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
120 participants
Enrollment target
1
Study location

Study Summary

Given the nationwide epidemic of opioid use and abuse (in part due to over prescription), this study aims at addressing the need for opioid prescription after laparoscopic hysterectomy.

Conditions Studied

Pain Pain, Postoperative Opioid Use Opioid Misuse

Interventions

  • DRUG Ibuprofen 600 mg
  • DRUG OxyCODONE 5 mg Oral Tablet
  • DRUG Acetaminophen 500 mg Tab

Study Locations (1)

Maryland

  • Johns Hopkins Hospital - Baltimore

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2023-01-12
Est. Completion 2026-12-31
Phase NA

Sponsor

Johns Hopkins University

1,448 total trials

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What the Registry Record Tells You About NCT05548582

The ClinicalTrials.gov registry entry for NCT05548582 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 304-participant average among 374 other Pain trials with a reported enrollment target (61% lower). The listed sponsor is Johns Hopkins University, which has 1,448 total studies on file at ClinicalTrials.gov.

The record links to 4 conditions, with Pain appearing as the primary indexed condition, and to 3 interventions - of which Ibuprofen 600 mg is the first listed.

NCT05548582 reports 1 study location spanning 1 distinct geographic area - top geographies include Maryland.

Frequently Asked Questions

What is clinical trial NCT05548582 about?

NCT05548582 is a clinical study titled "Reduced Opioid Prescription After Laparoscopic Hysterectomy". Given the nationwide epidemic of opioid use and abuse (in part due to over prescription), this study aims at addressing the need for opioid prescription after laparoscopic hysterectomy.

What is the current status of trial NCT05548582?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 120 participants. The study started on 2023-01-12. Estimated completion is 2026-12-31.

What conditions does trial NCT05548582 study?

This clinical trial studies the following conditions: Pain, Pain, Postoperative, Opioid Use, Opioid Misuse.

What interventions are being tested in trial NCT05548582?

The interventions under investigation include: Ibuprofen 600 mg (DRUG), OxyCODONE 5 mg Oral Tablet (DRUG), Acetaminophen 500 mg Tab (DRUG).

Who is sponsoring clinical trial NCT05548582?

This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05548582 being conducted?

This trial has 1 study location across Maryland. 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.