RECRUITING

Non-Narcotic Pain Control After ACL Reconstruction

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This is a double-blind randomized controlled trial of standard of care therapy, either oral ketorolac (experimental group) or oral oxycodone (control group) to demonstrate efficacy in reducing the percentage of narcotic doses taken and documenting the number of patients with no exposure to any narcotics (take zero oxycodone) after undergoing primary knee ACL reconstruction outpatient surgery.

Official Title

Non-Narcotic Pain Control After ACL Reconstruction

Quick Facts

Study Start:2025-05-15
Study Completion:2025-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06973785

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:15 Years to 55 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT
Inclusion CriteriaExclusion Criteria
  1. * Provision of signed and dated informed consent form
  2. * Stated willingness to comply with all study procedures and availability for the duration of the study
  3. * Male or female, aged 15-55 years
  4. * Primary Autograft ACL surgery
  5. * Ability to take oral medication and willingness to patriciate in a virtual 1 and 2 week follow-up pill counts
  1. * Provision of signed and dated informed consent form
  2. * Stated willingness to comply with all study procedures and availability for t the duration of the study
  3. * Male or female, aged 15-55 years
  4. * Primary Autograft ACL surgery
  5. * Ability to take oral medication and willingness to patriciate in a virtual 1 and 2 week follow-up pill counts

Contacts and Locations

Study Contact

Jennifer Baldwin
CONTACT
216.390.5833
baldwij3@ccf.org
Nick Niehart
CONTACT
nieharn@ccf.org

Principal Investigator

Kurt P Spindler, MD
PRINCIPAL_INVESTIGATOR
The Cleveland Clinic

Study Locations (Sites)

Cleveland Clinic Coral Springs
Coral Springs, Florida, 33067
United States
Cleveland clinic sports medicine
Garfield, Ohio, 44125
United States
Cleveland Clinic
Strongsville, Ohio, 44136
United States

Collaborators and Investigators

Sponsor: The Cleveland Clinic

  • Kurt P Spindler, MD, PRINCIPAL_INVESTIGATOR, The Cleveland Clinic

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-05-15
Study Completion Date2025-12-31

Study Record Updates

Study Start Date2025-05-15
Study Completion Date2025-12-31

Terms related to this study

Keywords Provided by Researchers

  • acl
  • Narcotic use

Additional Relevant MeSH Terms

  • ACL - Anterior Cruciate Ligament Rupture
  • ACL Injuries