1500 Participants Needed

Standard Care for Shoulder Injuries

Recruiting at 2 trial locations
HT
CR
Overseen ByColleen Roden, MS
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Stryker Endoscopy
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to gather data on patients who have undergone joint surgery using Stryker implants. As a retrospective study, it examines existing patient records to understand the outcomes of these surgeries. Patients who had joint space repair with one of these implants more than six months ago might be suitable candidates. The trial does not involve new treatments or surgeries; it reviews past procedures to ensure the implants perform well in everyday practice. As an unphased trial, it provides an opportunity to contribute to research that could enhance future patient care.

Do I need to stop my current medications for this trial?

The trial information does not specify whether you need to stop taking your current medications. It might be best to discuss this with the trial coordinators or your doctor.

Why are researchers excited about this trial?

Researchers are excited about the Stryker implants because they introduce advanced design features that aim to improve surgical outcomes. Unlike traditional implants, which often focus solely on structural support, these implants are crafted with materials and shapes designed to enhance integration with the body's tissues, potentially reducing recovery time and increasing the durability of the repair. This could mean fewer complications and a faster return to activity for patients, making it a promising option compared to standard surgical solutions.

Are You a Good Fit for This Trial?

Inclusion Criteria

I have had surgery to fix joint space with a specific device.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

Retrospective Data Collection

Data is collected retrospectively from standard practice records to assess clinical outcomes

6 months

Follow-up

Participants are monitored for safety and effectiveness after treatment

6 months

What Are the Treatments Tested in This Trial?

Interventions

  • Standard of Care Treatment

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Study SubjectsExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Stryker Endoscopy

Lead Sponsor

Trials
5
Recruited
2,000+