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NCT06511232 · ClinicalTrials.gov registry record · Phase 4

Intraosseous Morphine Administration During Anterior Cruciate Ligament Reconstruction

A Phase 4 study of Anterior Cruciate Ligament Injuries and Anterior Cruciate Ligament Tear, sponsored by The Methodist Hospital Research Institute.

Recruiting
Registry status
Phase 4
Development phase
84
Enrollment target
1
Study location

NCT06511232 is a Phase 4 study of Anterior Cruciate Ligament Injuries and Anterior Cruciate Ligament Tear that is actively recruiting participants, run by The Methodist Hospital Research Institute. The registered enrollment target is 84 participants, below the 320-participant average among 24 other Anterior Cruciate Ligament Injuries trials with a reported enrollment target (74% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06511232, a Phase 4 study of Anterior Cruciate Ligament Injuries and Anterior Cruciate Ligament Tear, is actively recruiting participants, sponsored by The Methodist Hospital Research Institute.

RECRUITING
Registry status
Phase 4
Development phase
84 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to determine if intraosseous (IO) morphine decreases pain and post-operative opioid use in patients undergoing anterior cruciate ligament (ACL) reconstruction.

Interventions

  • DRUG Intraosseous Morphine

Study Locations (1)

Texas

  • Houston Methodist Research Institute - Houston

Trial Details

FieldValue
Enrollment Target 84 participants
Start Date 2024-08-19
Est. Completion 2029-07-31
Phase Phase 4

What the Registry Record Tells You About NCT06511232

The ClinicalTrials.gov registry entry for NCT06511232 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 84 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 320-participant average among 24 other Anterior Cruciate Ligament Injuries trials with a reported enrollment target (74% lower). The listed sponsor is The Methodist Hospital Research Institute, which has 126 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Anterior Cruciate Ligament Injuries appearing as the primary indexed condition, and to 1 intervention - of which Intraosseous Morphine is the first listed.

NCT06511232 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT06511232 about?

NCT06511232 is a clinical study titled "Intraosseous Morphine Administration During Anterior Cruciate Ligament Reconstruction". The purpose of this study is to determine if intraosseous (IO) morphine decreases pain and post-operative opioid use in patients undergoing anterior cruciate ligament (ACL) reconstruction.

What is the current status of trial NCT06511232?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 84 participants. The study started on 2024-08-19. Estimated completion is 2029-07-31.

What conditions does trial NCT06511232 study?

This clinical trial studies the following conditions: Anterior Cruciate Ligament Injuries, Anterior Cruciate Ligament Tear, Anterior Cruciate Ligament Rupture.

What interventions are being tested in trial NCT06511232?

The interventions under investigation include: Intraosseous Morphine (DRUG).

Who is sponsoring clinical trial NCT06511232?

This trial is sponsored by The Methodist Hospital Research Institute, which has 126 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06511232 being conducted?

This trial has 1 study location across Texas. 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

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