RecruitingNot ApplicableNCT06876350

Woodcasting Versus Thermoplast Splint in CMC Arthroplasty

Patient Satisfaction for Post-Operative Carpometacarpal Arthroplasty: Wood Casting Versus Thermoplastic Splint


Sponsor

Foundation for Orthopaedic Research and Education

Enrollment

26 participants

Start Date

Oct 3, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This study is a prospective, randomized, nonblinded trial to evaluate patient preference in splints after having a carpometacarpal arthroplasty.


Eligibility

Min Age: 18 Years

Inclusion Criteria4

  • Patients over the age of 18 years old.
  • Intact Medical Decision Making
  • Eligible for Surgical Intervention
  • Willing to comply with all aspects of the treatment and evaluation schedule over 6 weeks

Exclusion Criteria2

  • Pregnant Women
  • Deemed Unsuitable by Principal Investigator

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Interventions

OTHERWoodcasting Splint

This is the experimental group so we could see the outcomes and preference for patients using surveys and compliance scores

OTHERControl (Standard treatment)

Thermoplastic splints are standard of care treatment for patients after CMC arthroplasty. We will use the data from this group as the comparator to the experimental group.


Locations(1)

Florida Orthopaedic Institute

Tampa, Florida, United States

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NCT06876350