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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04830917
Other study ID # SVMC 17-328
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 24, 2017
Est. completion date April 28, 2021

Study information

Verified date April 2022
Source Orthopaedic Specialty Group PC, Fairfield
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Comparing outcomes of individuals treated with Kinesiotape and oval 8 versus quick cast for a conservatively managed mallet finger injury. Outcomes include DIP joint extension lag, patient satisfaction and function via the MHQ.


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date April 28, 2021
Est. primary completion date April 28, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - determined by a physician to require conservative treatment for a mallet finger injury, at least 18 years of age Exclusion Criteria: - previous injury to the involved digit impacting ROM

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Immobilization type for mallet injury
Method to hold the DIP joint in full extension to allow healing of terminal tendon injury/mallet injury

Locations

Country Name City State
United States Orthopaedic Specialty Group PC Fairfield Connecticut

Sponsors (1)

Lead Sponsor Collaborator
Orthopaedic Specialty Group PC, Fairfield

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Goniometric measurement of range of motion for distal interphalangeal joint extension lag at the involved digit 12 weeks from injury
Secondary Goniometric measurement of range of motion for distal interphalangeal joint extension lag at the involved digit 6 months post injury
Secondary Brief Michigan Hand Outcome Questionnaire 12 weeks from injury
Secondary Brief Michigan Hand Outcome Questionnaire 6 months post injury
Secondary Satisfaction on a visual analog scale (0-10) 12 weeks from injury
Secondary Satisfaction on a visual analog scale (0-10) 6 months post injury
Secondary Goniometric measurement of range of motion deficit for distal interphalangeal joint flexion for involved digit 12 week post injury
Secondary Goniometric measurement of range of motion deficit for distal interphalangeal joint flexion for involved digit 6 months post injury
Secondary Pain according to a numeric pain rating scale (0-10/10) 12 weeks after injury
Secondary Pain according to a numeric pain rating scale (0-10/10) 6 months post injury