Is NCT04809064 recruiting in Bethesda, MD?

Yes, NCT04809064 is currently recruiting participants at its Bethesda, MD location. This shoulder dislocation clinical trial is actively enrolling qualified participants.

How do I join the shoulder dislocation clinical trial in Bethesda?

To join this clinical trial in Bethesda, complete the eligibility form on this page. A study coordinator will contact you to discuss next steps and determine if you qualify.

Is participation in this Bethesda clinical trial free?

Yes, all study-related care is provided at no cost to qualified participants. Many studies also offer compensation for time and travel expenses.

Shoulder Dislocation Clinical Trial in Bethesda, MD

About This Shoulder Dislocation Study in Bethesda

This clinical trial will determine the outcome trajectories of common surgeries (arthroscopic Bankart repair with remplissage of a Hill-Sachs lesion, open Bankart, Latarjet) with post-operative rehabilitation and identification of prognostic factors among patients with acute or recurrent anterior shoulder instability with subcritical bone loss. The results of the study assist in optimizing time to return to military duty, work and sports, and patient-reported physical function for military personnel and civilians with traumatic anterior shoulder instability and 10-20% glenoid bone loss. This study will provide a critical clinical advancement of a previously unaddressed and common clinical scenario.

Sponsor: University of Pittsburgh

Who Can Participate

Inclusion Criteria

Civilians and military personnel ages 17 to 50

Traumatic anterior shoulder dislocation

Associated subcritical bone loss between 10-20% less the glenoid width quantified by standard of care CT scan, MRI, or 3D-MRI scan

Had shoulder instability surgery using either 1) arthroscopic Bankart repair with remplissage of Hill-Sachs lesion; 2) open Bankart; or 3) Latarjet

Exclusion Criteria

Chronic, non-traumatic multi-directional instability based on clinical exam

Concurrent shoulder injury in the involved shoulder (e.g., rotator cuff tears, motor nerve pathologies, osteoarthritis of a Samilson-Prieto grade \>2)

Have a history of shoulder surgery in the involved shoulder (prior instability surgery that included any of the following and the planned procedure would be a repeat of the index procedure: 1) arthroscopic Bankart repair with a remplissage of Hill-Sachs lesion, 2) open Bankart, or 3) Latarjet \[previous isolated arthroscopic Bankart repair only would not be an exclusion criterion\], rotator cuff repair, intra-articular soft tissue surgery); rotator cuff repair, intra-articular soft tissue surgery)

Prior rotator cuff procedure on involved shoulder (including intra-articular soft tissue surgery

Humeral sided bone lesions (Hill-Sachs lesion) that is sufficiently large enough to render the lesion "off-track" even after a bony augmentation procedure would be performed

Neuromuscular, neurological and other movement control pathologies including seizures

Vascular injury associated with the shoulder trauma that compromise adequate/normal healing or interferes with usual course of care

Traumatic brain injury or any condition that would preclude the ability to comply with post-operative guidelines

Cartilage lesion finding in the involved shoulder that would interfere with usual course of care

Known pregnancy at time of imagining and/or surgery based upon standard of care testing procedures

Any issue with the contralateral shoulder that would preclude participation in research procedures

Any condition in the opinion of the investigator/clinician that would preclude or limit full participation in study activities

Absence of a fixed address or no means of contact

Known inability to be available at all follow-up time points

Does not plan to return to pre-injury levels of work, sports or military duty

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Bethesda?

Yes, this clinical trial (NCT04809064) has an active research site in Bethesda, MD that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Shoulder Dislocation Treatment Options in Bethesda, MD

If you're searching for shoulder dislocation treatment options in Bethesda, MD, this clinical trial (NCT04809064) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Bethesda research site is actively enrolling participants for this clinical trial. You'll receive care from experienced shoulder dislocation specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Shoulder Dislocation Clinical Trial in Bethesda, MD

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