RECRUITING

Ketorolac vs Oxycodone for Great Toe Arthrodesis

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 study reviews if taking ketorolac, after a joint fusion procedure, can decrease the need for taking oxycodone (standard of care) for pain relief. The study also investigates if ketorolac affects bone healing after surgery.

Official Title

Effect of Ketorolac Administration on Post-operative Narcotic Utilization and Union Rates in Great Toe Arthrodesis

Quick Facts

Study Start:2020-04-14
Study Completion:2024-07-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05054868

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:18 Years to 75 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age 18 - 75 years.
  2. * Women of childbearing potential must have a negative serum or urine pregnancy test results within 24 hours before the first dose of ketorolac.
  3. * Primary elective great toe MTP arthrodesis (CPT 28750). Other forefoot procedures often performed in conjunction with toe fusion will be included (CPT codes 28308, 28285, 28270).
  1. * Chronic pain syndrome, CRPS or fibromyalgia
  2. * Revision procedures
  3. * Use of allograft bone at the fusion site
  4. * Tobacco use
  5. * Diabetes
  6. * Narcotic abuse or IV drug abuse
  7. * Any CPT codes involving the midfoot, hindfoot, and/or ankle
  8. * Unable to take NSAIDs secondary to medical comorbidities such as kidney disease (impaired renal function with CrCl ≤ 50 ml/min) or gastric ulcers
  9. * Weight \< 50 kg
  10. * Does not speak or read English
  11. * If pregnant or planning to become pregnant or breastfeeding
  12. * Non-independent dweller (prisoner)

Contacts and Locations

Study Contact

Amy Loveland
CONTACT
3015602937
amy.loveland@medstar.net
Crisanto Macaraeg
CONTACT
410-261-8218
crisanto.l.macaraeg@medstar.net

Study Locations (Sites)

Amy Loveland
Baltimore, Maryland, 21218
United States

Collaborators and Investigators

Sponsor: Medstar Health Research Institute

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 Date2020-04-14
Study Completion Date2024-07-31

Study Record Updates

Study Start Date2020-04-14
Study Completion Date2024-07-31

Terms related to this study

Keywords Provided by Researchers

  • big toe arthrodesis
  • big toe
  • joint fusion

Additional Relevant MeSH Terms

  • Arthrodesis