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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04807322
Other study ID # RTSA in very old patients
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 24, 2019
Est. completion date December 21, 2020

Study information

Verified date March 2021
Source Bürgerspital Solothurn
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Reverse total shoulder arthroplasty (RTSA) has become an established treatment for cuff arthropathy, severe osteoarthritis and in certain fracture cases. Due to the increasingly aging population, patients who have already exceeded their life-expectancy pose a significant challenge to the shoulder surgeon. Therefore, we wanted to investigate patient demographics, hospital stay length, complication rate functional outcome, patient reported outcome scores and mortality retrospectively for patients, who were older than 83 years at time of implantation of a RTSA.


Description:

This is a retrospective single institution study. All patients older than 83 years who received a reverse shoulder arthroplasty from 2008 until 2019 are included. Elective cases are compared to fracture cases (patient demographics, length of hospital stay, complication rate, functional outcome, patient reported outcome scores and mortality).


Recruitment information / eligibility

Status Completed
Enrollment 110
Est. completion date December 21, 2020
Est. primary completion date August 4, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 83 Years and older
Eligibility Inclusion Criteria: - Patients older than 83 years at time of surgery - Patients who received a reverse total shoulder arthroplasty Exclusion Criteria: - Patients younger than 83 years at time of surgery

Study Design


Related Conditions & MeSH terms

  • Reverse Total Shoulder Arthroplasty

Intervention

Procedure:
Reverse Total Shoulder Arthroplasty (RTSA)
Implantation of a Reverse Total Shoulder Arthroplasty

Locations

Country Name City State
Switzerland Bürgerspital Solothurn Solothurn

Sponsors (1)

Lead Sponsor Collaborator
Bürgerspital Solothurn

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Patient reported outcome score: ASES American Shoulder and Elbow Society (ASES) Score until august 2020
Primary Complication rate postoperative complications requiring surgical intervention until august 2020
Primary Quality adjusted life year (QALY) The quality adjusted life year (QALY) ) is a well-established indicator of the life quality for the remaining years and was calculated as the years of life following the operation, multiplied by the utility value, for the current study, defined as the postoperative American Shoulder and Elbow Surgeons Shoulder Score (ASES) score (0-1 points) at last follow-up. until august 2020
Primary Mortality Survivership until august 2020
Primary Patient reported outcome score: QuickDASH Quick Disabilities of the arm, shoulder and hand (DASH) Score, until august 2020
Primary Patient reported outcome score: VAS Visual analog score (VAS) until august 2020
Secondary Patient demographics male/female ratio, age, BMI, ASA (American Society of Anesthesiologists) classification, hospital stay length, range of motion at time of surgery
See also
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Completed NCT02569658 - Investigation of Intravenous Tranexamic Acid With Anatomic and Reverse Total Shoulder Arthroplasty N/A
Enrolling by invitation NCT05789784 - Study of Zimmer Biomet Mymobility Application on Reverse Total Shoulder Arthroplasty (RTSA) Outcomes N/A
Not yet recruiting NCT06292169 - Pectoralis Minor Release Versus Non-release in RSA N/A
Completed NCT02052466 - Prediction of Development of Scapular Notching Following Reverse Total Shoulder Arthroplasty N/A
Recruiting NCT06133920 - Duration of Immobilization After Reverse Total Arthroplasty for Proximal Humerus Fractures
Enrolling by invitation NCT02014350 - Outcomes Following Delta Xtend Reverse Shoulder System N/A