MedTrace Logo

Functional and Radiographic Outcomes After Shoulder Surgery

NCT01405781 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1034

Last updated 2025-01-13

No results posted yet for this study

Summary

The objective of this study is twofold: First, to determine whether higher levels of pre-operative psychological distress predict worse outcomes after arthroscopic rotator cuff repair; second, to obtain functional outcomes (VAS pain, VAS satisfaction, VAS function, Simple Shoulder Test (SST) and American Shoulder and Elbow Surgeons (ASES) Score), physically examine and perform a radiographic analysis of patients at a minimum of 6 months after reverse total shoulder arthroplasty, total shoulder arthroplasty, arthroscopic scapulothoracic bursectomy, acromioclavicular joint reconstruction and arthroscopic rotator cuff repair.

Conditions

  • Shoulder Pain
  • Osteoarthritis of Glenohumeral Joint
  • Rotator Cuff Tear Arthropathy

Sponsors & Collaborators

Principal Investigators

  • Robert z Tashjian, MD · University Of Utah Orthopedics Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-05-31
Primary Completion
2024-09-13
Completion
2024-09-13

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

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 NCT01405781 on ClinicalTrials.gov