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Enrolling by invitation NCT06868108

Clinical Trial on the Effect of the Flexible Suturing System With Anchors (FSSA) in Full-thickness Rotator Cuff Tendon Tears

— Observational Rotator Cuff Tears

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Flexible Suturing System with Anchors (FSSA).
Who it may be relevant to
Registry conditions: Rotator Cuff Tears. Basic parameters: 18 years — 70 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The purpose of this research study is to evaluate tendon healing when using the Flexible Suturing System with Anchors (FSSA) to surgically repair full-thickness rotator cuff tendon tears.

Interventions

  • Device Flexible Suturing System with Anchors (FSSA)
    Surgically repaired full-thickness rotator cuff tendon tears with the Flexible Suturing System with Anchors (FSSA).

Primary outcome measures

  • Healing Rate [Time frame: One year]

Eligibility criteria

Inclusion criteria

Subjects MUST meet ALL the following criteria to be included in the study:

  • Underwent surgery to repair a torn rotator cuff tear with the Flexible Suturing System with Anchors (FSSA) and is able to obtain a follow-up MRI within 12 months +4 months / -1 month from the surgery date.
  • Tear size of the supraspinatus (SSP) with or without involvement of the infraspinatus (ISP), confirmed intra-operatively or with the pre-procedural MRI, is greater than or equal to 1 cm.
  • Between 18 and 70 years old at the time of surgery.
  • Able to understand the content of the subject information / Informed Consent Form (ICF) and is willing and able to participate in the prospective data collection protocol and comply with the required data collection.

Exclusion criteria

Subjects will be excluded from the study if they meet ANY of the following criteria:

  • Had a prior rotator cuff surgery on the index shoulder.
  • Has a subscapularis tear with a Lafosse score of 3 or greater, or a teres minor tear requiring repair.
  • Identified as being repaired in a hybrid approach, where a non-FSSA anchor is used in the case for SSP and/or ISP rotator cuff repair.
  • SSP and / or ISP tendon ruptures that are considered irreparable or only partially repairable at the time of the intervention.
  • At any time during the previous 18 months was involved in a workers compensation case or litigation related to bodily injury, whether related or unrelated to the index shoulder.
  • Has a history of chronic opioid use.
  • Subjects with condition(s) that contraindicate or complicate outcomes of ARCR such as:
  • Current or prior infection of the ipsilateral shoulder
  • Known inflammatory arthropathy or history of inflammatory arthropathy
  • Chronic joint disease
  • Concomitant labral fixation
  • Concomitant os acromial fixation
  • Glenohumeral joint instability (multiple dislocations/subluxations)
  • Subacromial or intra-articular injection within 3 months prior to surgery
  • Oral or injected steroid use in the following timeframe: 4 weeks prior to surgery through current date
  • Hamada 3 or greater rotator cuff arthropathy on X-ray
  • Goutallier atrophy > Grade 3
  • Proximal humeral fracture or scapular fracture
  • Avascular necrosis of humeral head or glenoid
  • Immunodeficiency disorders
  • Chronic inflammatory disorders
  • Osteoarthritis >2 (Samilson-Prieto)
  • Has other concurrent medical or other conditions (chronic or acute in nature) that in the opinion of the participating investigator may prevent participation or otherwise render subject ineligible for the study.
  • Subjects who are unable to tolerate magnetic resonance imaging (MRI), due to psychiatric or medical contraindications.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

United States · 3 centers
  • OrthoCarolina Research Institute — Charlotte
  • Texas Orthopedic Specialist — Bedford
  • Houston Methodist The Woodlands — The Woodlands

Identifiers

NCT: NCT06868108 · DN-00808

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗