Woodcasting Versus Thermoplast Splint in CMC Arthroplasty

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorFoundation for Orthopaedic Research and Education

About this trial

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

Eligibility criteria

Qualifiers

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

Disqualifiers

Pregnant Women

Deemed Unsuitable by Principal Investigator

Trial design

Treatments tested in this trial

  • Woodcasting Splint
  • Control (Standard treatment)

Treatment groups

26 Participants
are divided into 2 treatment groups