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Intraosseous Morphine Administration During Anterior Cruciate Ligament Reconstruction

The Methodist Hospital Research Institute (TMHRI) logo

The Methodist Hospital Research Institute (TMHRI)

Status and phase

Enrolling
Phase 4

Conditions

Anterior Cruciate Ligament Injuries
Anterior Cruciate Ligament Tear
Anterior Cruciate Ligament Rupture

Treatments

Drug: Intraosseous Morphine

Study type

Interventional

Funder types

Other

Identifiers

NCT06511232
PRO00037918

Details and patient eligibility

About

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.

Enrollment

84 estimated patients

Sex

All

Ages

18 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients of the IRB approved surgeon(s) undergoing ACL reconstruction with bone-to-bone (BTB) autograft
  • Patients aged between 18-40 years old at the time of surgery

Exclusion criteria

  • Patients undergoing ACL reconstruction with any other type of autograft or allograft other than BTB
  • Patients younger than 18 years old or older than 40 years old
  • Patients undergoing meniscal root repair or any other repair that changes their weight-bearing status
  • Patients with a history of substance abuse
  • Vulnerable populations
  • Patients on chronic pain medication within the last 6 months
  • BMI >/= 35
  • Allergy to morphine
  • Unwilling to participate
  • Any additional reason the PI deems reasonable

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

84 participants in 2 patient groups

Intraosseous Injection of Morphine
Experimental group
Description:
The intervention group will receive an intraosseous (IO) injection of 10mg of morphine mixed with up to 100mg of saline into the tibial tubercle during a standard ACL reconstruction.
Treatment:
Drug: Intraosseous Morphine
Standard of Care Morphine Administration
No Intervention group
Description:
The control group will receive the standard of care treatment, which is no IO injection during a standard ACL reconstruction.

Trial contacts and locations

1

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Central trial contact

Haley Goble, MHA

Data sourced from clinicaltrials.gov

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