Overview
This study is a prospective, randomized, nonblinded trial to evaluate patient preference in splints after having a carpometacarpal arthroplasty.
Description
Patients undergoing carpometacarpal arthroplasty will be randomized into the woodcast or thermoplast splint after their surgery to see which is preferred using compliance and surveys.
Eligibility
Inclusion Criteria:
- 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 Criteria:
- Pregnant Women
- Deemed Unsuitable by Principal Investigator