NCT00284388

Brief Summary

Development of a non-invasive method for the determination of the position of optimal muscle length in the different muscles of the shoulder. Analysis of the adaptation of the muscle to a new optimal length in patients with a shoulder prosthesis.

Trial Health

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 30, 2006

Completed
1 day until next milestone

First Posted

Study publicly available on registry

January 31, 2006

Completed
Last Updated

July 7, 2021

Status Verified

July 1, 2021

First QC Date

January 30, 2006

Last Update Submit

July 5, 2021

Conditions

Shoulder Prosthesis

Outcome Measures

Primary Outcomes (1)

  • Measurement of the optimal length of the muscles of the shoulder

Interventions

Simultaneous controlled power measurementPROCEDURE
Surface EMG measurementPROCEDURE

Eligibility Criteria

Age40 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Shoulder prosthesis

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Links

Study Officials

  • Rene Verdonk, MD, PhD

    University Hospital, Ghent

    PRINCIPAL INVESTIGATOR
0

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 30, 2006

First Posted

January 31, 2006

Last Updated

July 7, 2021

Record last verified: 2021-07