Intraosseous Morphine Administration During Anterior Cruciate Ligament Reconstruction
- Conditions
- Anterior Cruciate Ligament TearAnterior Cruciate Ligament InjuriesAnterior Cruciate Ligament Rupture
- Registration Number
- NCT06511232
- Lead Sponsor
- The Methodist Hospital Research Institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 84
Inclusion Criteria:<br><br> - Patients of the IRB approved surgeon(s) undergoing ACL reconstruction with<br> bone-to-bone (BTB) autograft<br><br> - Patients aged between 18-40 years old at the time of surgery<br><br>Exclusion Criteria:<br><br> - Patients undergoing ACL reconstruction with any other type of autograft or allograft<br> other than BTB<br><br> - Patients younger than 18 years old or older than 40 years old<br><br> - Patients undergoing meniscal root repair or any other repair that changes their<br> weight-bearing status<br><br> - Patients with a history of substance abuse<br><br> - Vulnerable populations<br><br> - Patients on chronic pain medication within the last 6 months<br><br> - BMI >/= 35<br><br> - Allergy to morphine<br><br> - Unwilling to participate<br><br> - Any additional reason the PI deems reasonable
Not provided
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Patient Pain Levels in the Post-Operative Period as assessed by a patient-reported post operative symptom journal.;Changes in Post-Operative Opioid Use;Patient Pain Levels in the Post-Operative Period as assessed by the Lysholm Knee Survey
- Secondary Outcome Measures
Name Time Method Patient Range of Motion in the Post-Operative Period as assessed by the KOOS, JR. Knee Survey;Patient Activity Level in the Post-Operative Period as assessed by the Tegner scale.;Patient Range of Motion in the Post-Operative Period as assessed by the Lysholm Knee Survey