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Objective Evaluation of Shoulder Pathology and Surgery

NCT00500630 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL

Last updated 2007-07-13

No results posted yet for this study

Summary

The goal of this study was to clinically validate a new device for the objective outcome evaluation of adult patients undergoing shoulder surgery for glenohumeral osteoarthritis and rotator cuff disease, using the activities of daily living described in the Simple Shoulder Test (SST) as a reference.

The study was set up as a clinical trial including patients over an observation period of one year and a control group of subjects. Clinical evaluations will be made at baseline, 3 months, 6 months and 1 year after surgery by two independent observers. Miniature sensors each containing three 3D gyroscopes and three 3D accelerometers will allow computing new kinematic scores. They will be compared to the regular SST, DASH, ASES and Constant scores.

Conditions

  • Glenohumeral Osteoarthritis
  • Rotator Cuff Disease

Interventions

DEVICE

Body fixed 3D sensors

Sponsors & Collaborators

  • University of Lausanne Hospitals

    lead OTHER

Principal Investigators

  • Brigitte M Jolles, MD, MSc · Centre Hospitalier Universitaire Vaudois - University of Lausanne

Study Design

Allocation
NON_RANDOMIZED
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00500630 on ClinicalTrials.gov