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

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. According to ClinicalTrials.gov, the official US trial registry.

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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.

Primary Outcome

The study will measure patient-reported levels of pain on a daily basis (for a total of two weeks) with a symptom journal, which will ask patients to report on a variety of pain-related outcomes including levels of pain throughout different times of day, levels of nausea throughout different times of the day, and what pain medication(s) they are taking and at what time.

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 NCT06511232 shows while recruiting

NCT06511232 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 84 participants, a relatively small participant target, below the 320-participant average among 24 other Anterior Cruciate Ligament Injuries trials with a reported enrollment target (74% lower).

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 a single indexed study location in 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.

Similar trials for Anterior Cruciate Ligament Injuries

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06511232's enrollment target sits among peer trials

84 12th of 24 higher than 13 of 24 other Anterior Cruciate Ligament Injuries trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Anterior Cruciate Ligament Injuries trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06511232, the US trial registry maintained by the National Library of Medicine. NCT06511232 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.