Recruiting

Shoulder Arthroplasty

Sponsor:

Hospital for Special Surgery, New York

Code:

NCT00527839

Conditions

Shoulder Arthroplasty

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Study Details

Brief summary:

Total joint replacements are some of the most successful medical devices developed over the last fifty years. They enable millions of people to remain ambulatory and pain free, with minimal risk. In 2002, over 200,000 total hip replacements, 350,000 total knee replacements, and 25,000 total or partial shoulder replacements were performed in the United States (HCUP data). Future use will likely be even higher: it is estimated that by the year 2020, the population 65 and over in developed countries will increase by 71%. Existing studies do not provide adequate prospective data to evaluate long-term outcomes.

HSS is a world leader in total joint replacement including total shoulder arthroplasty. However, there is no systematic follow-up or evaluation of patients who have their shoulders replaced here.

The purpose of this study is to establish a prospective cohort of HSS total shoulder arthroplasty to evaluate predictors of outcome, causes of failure and to allow ongoing evaluation of the results of our patients over time.

Conditions

Shoulder Arthroplasty

Study ID

NCT00527839

Start date

Apr, 2007

Status verified date

Nov, 2025

Completion date

Apr, 2027

Anticipated

Primary completion date

Apr, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • 18 years or older and undergoing total shoulder arthroplasty at HSS

Exclusion Criteria:

  • No other exclusion criteria. Pregnant women are eligible for the registry as this is a non-interventional study which only involves filling out questionnaires.

Study Design

Enrollment

250 participants

Anticipated

Interventions and Outcome Measures

Primary outcome measure

  • Patient Reported Outcome Measures (PROMs) [ Time Frame: Collection of at Baseline, 6 Months, 1 Year, 2 Year, 5 Year and 10 Year ]
  • Intra Operative Data [ Time Frame: Collection of data on Day 0 (Date of Surgery) ]
  • Demographic data [ Time Frame: Collection of at Baseline, 6 Months, 1 Year, 2 Year, 5 Year and 10 Year ]

Central Contacts and Locations

Central contacts

Locations

Hospital for Special Surgery

Recruiting

New York, New York, United States, 10021

Contacts

Kaitlyn Lillemoe

lillemoek@hss.edu

Principal Investigator:

Robert Marx, MD

Hospital for Special Surgery

Recruiting

New York, New York, United States, 10021

Contacts

More Information

Sponsor

Hospital for Special Surgery, New York

Last update posted

Feb 12, 2026

Last verified

Nov, 2025

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Hospital for Special Surgery, New York on 2026-02-12.