Prophylactic Conjoint Tendon Lengthening During Reverse Shoulder Arthroplasty Outcomes

This study is looking at ways to prevent shoulder pain after a reverse shoulder replacement surgery (Reverse Shoulder Arthroplasty). Some people experience pain in the front of their shoulder because the surgery can put extra stress on a tendon called the conjoint tendon. This study will compare two surgical approaches: a standard reverse shoulder arthroplasty, and a reverse shoulder arthroplasty where the conjoint tendon is also lengthened. Researchers want to see if lengthening the conjoint tendon can reduce or prevent this pain one year after surgery. You may be able to join if you are at least 18 years old and are having your first reverse total shoulder arthroplasty at specific Loyola hospitals. The study plans to enroll 110 participants, but its current status is unclear.

Study design
This is an interventional study comparing two surgical procedures. It plans to enroll 110 participants.
What's involved
Participants will undergo either a standard reverse shoulder arthroplasty or a reverse shoulder arthroplasty with conjoint tendon lengthening. Your shoulder health will be assessed from enrollment until 12 months after treatment.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for 12 months after their treatment to assess their shoulder health.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06729983

Prophylactic Conjoint Tendon Lengthening During Reverse Shoulder Arthroplasty Outcomes

Recruiting
NAAges 18+InterventionalTreatment
Nickolas Garbis
~110 participants
Updated 2025-03-07 on ClinicalTrials.gov
What's tested:Prophylactic Conjoint Tendon LengtheningStandard Reverse Shoulder Arthroplasty

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
American Society of Shoulder and Elbow Surgeons (ASES) Score
Measured over From enrollment to the end of treatment at 12 months
Osteoarthritis Shoulder

NCT06729983

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Loyola Outpatient Center

    Maywood, Illinoisstudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Nickolas G Garbis, MD · PRINCIPAL_INVESTIGATOR · Loyola University

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Eligibility criteria

Inclusion

Patients who are at least 18 years old undergoing primary reverse total shoulder arthroplasty
Operations that occur at Loyola University Medical Center (Maywood, IL), Loyola Ambulatory Surgery Center (Maywood, IL), or Gottlieb Memorial Hospital

Exclusion

Patients younger than 18 years old
Patients who had prior coracoid transfer procedure
Patients who are undergoing revision surgery from a prior arthroplasty
Current pregnancy As per standard protocol with all surgeries, a urine pregnancy test is performed prior to surgery. If positive, the surgery will be cancelled and the patient will be excluded from the research study.
  • American Society of Shoulder and Elbow Surgeons (ASES) ScoreFrom enrollment to the end of treatment at 12 months

    The ASES is a 100-point scale that consists of two dimensions: pain and activities of daily living. There is one pain scale worth 50 points and ten activities of daily living worth 50 points. The higher the points the better the outcome.