MedTrace Logo

From Rotator Cuff Repair to Reverse Shoulder Arthroplasty - Clinical and Radiological Results

NCT06644729 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 733

Last updated 2024-10-22

No results posted yet for this study

Summary

In the planned study the investigators will invite 733 participants 10 years after arthroscopic rotator cuff repair to a follow up examination.

Shoulder pain is a common problem in the Norwegian population. Rotator cuff tear is a major cause of shoulder pain with a reported prevalence of up to 51% in patients 60-80 years of age. Arthroscopic rotator cuff repair is performed in an increasing proportion of these patients. Good results in shoulder function has been reported, although there is a lack in published good quality studies and long term follow up of these patients. There is also a lack of evidence regarding the association between radiologically-verified re-tear and clinical outcome.

In this project, the investigators address these critical gaps in knowledge and aim to investigate the factors influencing the clinical outcome after rotator cuff surgery and re-tear in a large prospective cohort study. The investigators will investigate how many participants suffering from poor outcome and develop cuff arthropathy in need of reverse shoulder arthroplasty after 10 years.

Conditions

  • Rotator Cuff Tears
  • Rotator Cuff Tear Arthropathy
  • Rotator Cuff Injuries

Interventions

PROCEDURE

Arthroscopic Rotator Cuff Repair

Arthroscopic Rotator Cuff Repair

Sponsors & Collaborators

  • Sykehuset Telemark

    collaborator OTHER_GOV

  • South-Eastern Norway Regional Health Authority

    collaborator OTHER

  • Lovisenberg Diakonale Hospital

    lead OTHER

Principal Investigators

  • Kjersti Kaul Jenssen, MD, PhD · Lovisenberg Diaconal Hospital

Eligibility

Min Age
18 Years
Max Age
95 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-09-11
Primary Completion
2025-12-31
Completion
2025-12-31

Countries

  • Norway

Study Locations

More Related Trials

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 NCT06644729 on ClinicalTrials.gov