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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01876498
Other study ID # Brief MHQ1
Secondary ID Dupuytren 1
Status Completed
Phase N/A
First received June 10, 2013
Last updated August 19, 2016
Start date August 2013
Est. completion date July 2015

Study information

Verified date August 2016
Source Schulthess Klinik
Contact n/a
Is FDA regulated No
Health authority Switzerland: Ethikkommission
Study type Observational [Patient Registry]

Clinical Trial Summary

The purpose of this study is the validation of the Brief Michigan Hand Questionnaire by patient with Morbus Dupuytren and to build up a register.


Description:

examination of the characteristics of Patient with Morbus Dupuytren and the psychometric properties of the Brief Michigan Hand Questionnaire by this patients


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date July 2015
Est. primary completion date July 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- M.Dupuytren, over 18y, able to speak and understand german

Exclusion Criteria:

- recurrence, pregnancy, incapable of contracting

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Procedure:
Xiaflex surgery
Xiaflex surgery

Locations

Country Name City State
Switzerland Schulthess Klinik Zurich

Sponsors (1)

Lead Sponsor Collaborator
Schulthess Klinik

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Other Pain Measuring pain with the Numeric rating scale 3 years No
Other Grip Strength Measuring grip strength with the dynamometer 3 years No
Other Quick DASH Patient reported outcome measurement by arm, shoulder and hand disorders 3 year No
Other Euroqol 5l5d analysis of the costs and utilities 3 years No
Other Michigan Hand Questionnaire Patient reported outcome measurement by hand disorders 3 years No
Primary Brief Michigan Hand Questionnaire Patient reported outcome measurement by hand disorders 6 weeks No
Secondary Joint mobility Measuring the joint mobility of the fingers with the goniometer 3 years No
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