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Study Subjects for Shoulder Injuries

N/A
Recruiting
Research Sponsored by Stryker Endoscopy
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights

Study Summary

Retrospective, multi-center, chart review (only to include data that is part of the surgeons' standard practice)

Eligible Conditions
  • Shoulder Injuries
  • Hip Injury
  • Knee Injuries

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 6 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
ASES
iHOT-12
mHHS

Side effects data

From 2021 Phase 2 trial • 47 Patients • NCT04492891
13%
Chest pain - cardiac
3%
Investigations - Other, specify
3%
Headache
3%
Acute kidney injury
3%
Confusion
3%
Alanine aminotransferase increased
3%
Aspartate aminotransferase increased
3%
Vomiting
3%
Sepsis
3%
Ear pain
3%
Death NOS
3%
Respiratory, thoracic and mediastinal disorders - Other, specify
3%
Constipation
3%
Nausea
3%
Back pain
3%
Adult respiratory distress syndrome
3%
Hypoxia
100%
80%
60%
40%
20%
0%
Study treatment Arm
Arm A Cyclosporine
Arm B Standard of Care

Trial Design

1Treatment groups
Experimental Treatment
Group I: Study SubjectsExperimental Treatment1 Intervention
Patients who have undergone a surgical procedure (per product indications for use) using the Stryker implants who meet all of the following criteria will be screened and enrolled by participating Investigators.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Standard of Care Treatment
2016
Completed Phase 3
~410

Find a Location

Who is running the clinical trial?

Stryker EndoscopyLead Sponsor
4 Previous Clinical Trials
480 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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