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Continuous Passive Motion Versus Heterotopic Ossification

Study acronym: CPMversusHO
StatusRecruiting
PhaseNot applicable
Started
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Record status
This record was last updated December 6, 2024 (before its estimated April 25, 2026 completion). Its status may not reflect the trial's current state.

Record History

  1. Minor Re-verified, no change to tracked fieldsv3
  2. Minor Interventions: Continuous Passive Motion (CPM) (Device), Conventional physiotherapy (PT) (Other) to Continuous Passive Motion (CPM) (Device), Conventional physiotherapy (PT) (Other), Zoledronic Acid Injection (Drug)
    • Secondary endpoints: details revised at 1 of 1 entry
    v2
  3. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
3,531 trials monitored
See 153 trials at risk
The investigators hypothesize that Heterotopic Ossification (HO) formation can be suppressed if the application of a Continuous Passive Motion (CPM) device can be performed for a substantial amount of time. The investigators will use the following study design: a pilot study with 10 ICU patients receiving CPM and 10 matched cases which will follow a conventional physiotherapy program at the time of the conduction of the study. The comparison between the treatment and referent groups of the outcomes will prove the prophylactic power of CPM against HO.
Trial Details
NCT Number NCT05906056
Lead Sponsor University of Ioannina
Conditions
(from sponsor)
Traumatic Brain Injury, Spinal Cord Injuries, Stroke
Related terms Brain Injuries, Traumatic, Ossification, Heterotopic, Spinal Cord Injuries, Stroke
Enrollment 20 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov