Skip to main content
OpenTrials
Completed

NCT Number: NCT01877434

Reversed TESS Shoulder Artroplasty

Reverse total shoulder arthroplasty (RSA) is a accepted treatment for different shoulder diseases with improved functional outcome. This study has evaluated patients operated with reversed shoulder arthroplasty after 1,5-3 years postoperatively with patient reported outcome, clinical and radiological examination, complication and reoperations. The radiologic phenomenom and clinical impact of scapular notching (SN) and arm length difference has been evaluated.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Humerus Fracture Arm Injuries Degenerative Shoulder Pain Degenerative Supraspinatus Rupture Fractures, Bone Humeral Fractures Wounds and Injuries

Age range

60 year–88 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Institution of surgical and operative sciences, Umeå University

Sundsvall, Västernorrland Län, Sweden

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Operated with a reversed TESS total shoulder arthroplasty at Sundsvall hospital.

Exclusion criteria

  • Do not give informed consent
  • Do not attend follow-up

Treatment and study plan

Reversed shoulder arthroplasty

Procedure

Primary outcomes

  1. Patient reported outcome measurement Quick-DASH

    Time frame: 2007-2013

Secondary outcomes

  1. Range of movement

    Time frame: 2007-2013

  2. Quality of life EQ5-D

    Time frame: 2007-2013

Other outcomes

  1. Arm lenght difference

    Time frame: 2007-2013

    Impact on arm lenght difference on patient reported outcome evaluated with Quick-DASH

Sponsors and collaborators

Lead sponsor

Sundsvall Hospital

Other

Registry information

Official study title

The TESS Reverse Shoulder Arthroplasty: Effect of Arm Lengthening and Early Scapular Notching at Three Years Follow-up

Acronym: RTESS

Important dates

Study start
2007
Primary completion
2012
Study completion
2013
First posted
Jun 13, 2013
Registry last updated
Jun 13, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.