Skip to content

Woodcasting Versus Thermoplast Splint in CMC Arthroplasty

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06876350
Acronym
Woodcast
Enrollment
26
Registered
2025-03-14
Start date
2024-10-03
Completion date
2025-06-30
Last updated
2025-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Carpometacarpal (CMC) Joint Arthritis

Keywords

Randomized, Hand and Upper Extremity

Brief summary

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

Detailed 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.

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.

Sponsors

Foundation for Orthopaedic Research and Education
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Patient Satisfaction Score6 WeeksThe satisfaction survey consists of three questions totaling 15. The minimum value is a 1, while the maximum value is 15. A higher score indicating highest satisfaction.

Secondary

MeasureTime frameDescription
Waste2 WeeksEach splint group creates waste for the fabrication and molding for each patient which will be recorded by the clinical research coordinator and weighed out.
Splint Satisfaction6 WeeksPatient will have three questions totaling 15 with the higher score indicating highest satisfaction.
Splint Issues6 WeeksA single question will be filled out by patients on a scale of 1-5 with a score of 5 indicating a lot of issues with their splint.

Countries

United States

Contacts

Primary ContactAndy Nguyen, BS
anguyen@foreonline.org8139789700
Backup ContactDeborah Warren, RN
dwarren@foreonline.org8139789700

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026