RECRUITING

Continuous Passive Motion Following Fixation of Pelvic and Knee Fractures

Conditions

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

The investigators will directly compare the visual analog scale scores and narcotic pain medication requirements in the patients who have continuous passive motion (CPM) versus those who do not during the course of the hospital admission following an open reduction internal fixation surgery for acetabular fracture, supracondylar femur fracture, or a tibial plateau fracture.

Official Title

The Role of Continuous Passive Motion in Pain Control of Patients Undergoing Operative Management of Isolated Acetabular Fractures, Supracondylar Femur Fractures, or Tibial Plateau Fracture: A Comparative Study

Quick Facts

Study Start:2020-10-06
Study Completion:2026-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04389749

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
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age 18 or greater
  2. * Isolated acetabular fractures, supracondylar femur fractures, or tibial plateau fracture
  3. * Have undergone operative intervention for fracture
  1. * Injury to either lower extremity that affects the patient's ability to weight bear
  2. * Under the age of 18
  3. * Pregnant
  4. * A prisoner

Contacts and Locations

Study Contact

Kimberly A Hasselfeld, MS
CONTACT
513-558-1933
hasselky@uc.edu

Principal Investigator

Henry C Sagi, MD
PRINCIPAL_INVESTIGATOR
University of Cincinnati

Study Locations (Sites)

Univrsity of Cincinnati Medical Center
Cincinnati, Ohio, 45267
United States

Collaborators and Investigators

Sponsor: University of Cincinnati

  • Henry C Sagi, MD, PRINCIPAL_INVESTIGATOR, University of Cincinnati

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 Date2020-10-06
Study Completion Date2026-06

Study Record Updates

Study Start Date2020-10-06
Study Completion Date2026-06

Terms related to this study

Additional Relevant MeSH Terms

  • Fractures, Bone