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NCT01869244 Clinical Trial

WOODCAST Hand Resting Splint - Study of User Experience

Patient Satisfaction Clinical Trial

Official title:
User Experience From WOODCAST 2mm Hand Resting Splint

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01869244
Other study ID # 152/13/03/02/2013
Secondary ID
Status Completed
Phase N/A
First received May 31, 2013
Last updated June 13, 2017
Start date April 2013
Est. completion date September 2016

Study information
Verified date June 2017
Source Onbone Oy
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the study is to collect comments form users of new type of hand resting splint.

Description:

An ecologically friendly and biodegradable wood-plastic composite cast (WOODCAST) is used as a hand resting splint in this study.

Recruitment information / eligibility
Status Completed
Enrollment 18
Est. completion date September 2016
Est. primary completion date September 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- patient treatment involves hand resting splint; age of patient 18 - 90 years; skills with language Finnish language (written and spoken)

Exclusion Criteria:

- decreased co-operation of the patient; patient with multiple illnesses; malignancy; an illness affecting the general health.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Finland Kuntoutus Orton Oy Helsinki

Sponsors (1)
Lead Sponsor Collaborator
Onbone Oy

Country where clinical trial is conducted

Finland, 

Outcome
Type Measure Description Time frame Safety issue
Primary User satisfaction After using hand resting splint for two weeks, patient will fill a questionaire. In the questionaire patient is asked to assess the used splint (e.g. functional performance, visual appearance), by giving points (from 1 to 10 points). Patient will use two splints from different materials during the treatment (both of the splint will be assessed by the patient). 2-4 weeks
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