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NCT Number: NCT04389749

Continuous Passive Motion Following Fixation of Pelvic and Knee Fractures

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.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Univrsity of Cincinnati Medical Center

Cincinnati, Ohio, 45267, United States

Location status: Recruiting

Location contact

Henry Sagi, MD

CONTACT

5137776213

Kim Hasselfeld, MS

CONTACT

[email protected]

5137776213

About this study

This will be a prospective comparative cohort study analyzing the practices of three surgeons, one of whom routinely uses CPM following fixation of pelvic and acetabular fractures, and two surgeons who do not.

All patients, over the age of 18 years who have undergone open reduction and internal fixation (ORIF) of isolated acetabular fractures, supracondylar femur fractures, or tibial plateau fracture will be asked to participate. Those who consent will be randomized into two groups. The experimental group will have a CPM applied in the PACU immediately post-op and it will be utilized while the patient is awake in bed for 2 hours on and 2 hours off, when not mobilizing with Physical Therapy (PT). The experimental group will also have traditional PT, including sessions 1 to 3 times a week. The control group will have typical care, including working with physical therapy 1 to 3 times a week. The investigators will directly compare the VAS scores and narcotic pain medication requirements in the patients who have CPM versus those who do not during the course of the hospital admission. VAS scores will be assessed throughout the day by RN and/or PT. Functional outcomes will be assessed at the one-year mark using the Iowa and Majeed pelvic functional outcome tools along with the SF-12. Orthopedic Resident or Nurse Clinical will check the patient for incision integrity each day and each session of using the CPM, the patient will be monitored for adverse events. Data will be collected using Epic.

The investigators will record patient demographics including age, sex, and pre-existing narcotic usage. Fracture type according to the Orthopaedic Trauma Association will be recorded. VAS scores and pain medication requirements will be recorded from the first 48 hours during the patient's stay. Pain scores and CPM use will be obtained from Epic using the flowsheet.

Functional outcomes will be assessed at the one-year mark using the Iowa and Majeed pelvic functional outcome tools along with the SF-12.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 or greater
  • Isolated acetabular fractures, supracondylar femur fractures, or tibial plateau fracture
  • Have undergone operative intervention for fracture

Exclusion criteria

  • Injury to either lower extremity that affects the patient's ability to weight bear
  • Under the age of 18
  • Pregnant
  • A prisoner

Treatment and study plan

CPM

Device

CPM-continuous passive motion device.

Primary outcomes

  1. VAS Pain Score

    Time frame: Visual Analog Score for pain will be recorded daily after the surgery each day until the patient is discharged or up to 365 days..

    Pain will be assessed by the patient on a scale of 1-10 during hospitalization. 1=no pain; 10=worst pain

Secondary outcomes

  1. SF-12

    Time frame: This score will be completed at the one-year post-operative visit.

    The Short Form 12 (SF-12) uses just 12 questions to measure functional health and well-being from the patient's point of view. An algorithm is used to generate the physical and mental health composite scores for comparison to normative data. The mean score is set to 50. Scores >50 indicate better physical or mental health than to mean. Scores <50 indicate worse physical or mental health than the mean.

Study contacts

Contact information is provided by the study sponsor or research team.

Kimberly A Hasselfeld, MS

CONTACT

[email protected]

513-558-1933

Sponsors and collaborators

Lead sponsor

University of Cincinnati

Other

Registry information

Official study 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

Important dates

Study start
2020
Primary completion
2026
Study completion
2027
First posted
May 15, 2020
Registry last updated
May 4, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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