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Influence of Custom Orthosis Post Carpometacarpal (CMC) Arthroplasty

NCT05307510 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 21

Last updated 2024-10-08

Study results available
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Summary

This study aims to compare post-surgical outcomes of individuals who receive either a custom orthosis or prefabricated splint after carpometacarpal arthroplasty.

Conditions

  • Thumb Osteoarthritis

Interventions

DEVICE

Prefabricated splint

Subjects will be provided either a prefabricated splint

DEVICE

Custom Orthosis

Subjects will be evaluated by an occupational therapist who will fabricate a custom orthosis.

Sponsors & Collaborators

  • University of Toledo

    lead OTHER

Principal Investigators

  • Laura Schmelzer, PhD · The University of Toledo

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-04-21
Primary Completion
2023-10-27
Completion
2023-10-27
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05307510 on ClinicalTrials.gov