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Function Following Thumb MP Fusion and IP Fusion

Function Following Thumb MP Fusion and IP Fusion

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03661281
Enrollment
32
Registered
2018-09-07
Start date
2018-02-01
Completion date
2019-06-24
Last updated
2020-02-07

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

Conditions

Osteoarthritis

Brief summary

This study is to determine function following simulated thumb metacarpophalangeal (MP) and thumb interphalangeal (IP) joint fusion. The investigators want to determine the functional limitation created by MP and IP joint fusion. 20-30 volunteers will be fitted for custom molded orthoplast splints immobilizing either the MP or IP joint. The volunteers will then be taken through multiple tests including lateral pinch strength, tip pinch, grip strength, grooved pegboard test time, and Jebson Taylor test. Each patient will be tested without a splint, with their MP joint immobilized and with their IP joint immobilized. The results of this study can be used for patient education before surgery in order to help them make informed decisions as well as manage expectations. It can also serve as a decision aid in pinch restoration in the context of ulnar nerve palsy.

Interventions

DIAGNOSTIC_TESTGrooved pegboard test

Time will be measured and compared between control, MP splint and IP splint

consists of seven test items, which are felt to represent various hand activities. These test items include: writing a short sentence; turning over 365 inch cards; picking up small objects and placing in a container; stacking checkers; simulated eating; moving empty large cans; and moving weighted large cans.

DIAGNOSTIC_TESTPinch strength

Measured in every splint position using a standard dynamometer

Sponsors

NYU Langone Health
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Patient is a healthy volunteer * Patient is willing and able to review and sign a study informed consent form

Exclusion criteria

* Any subject who does not want to voluntarily participate.

Design outcomes

Primary

MeasureTime frameDescription
Jebsen Taylor hand function test1 MonthThis consists of seven test items, which are felt to represent various hand activities. Each activity will be timed.

Countries

United States

Outcome results

None listed

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