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SINEFIX-2022 Pilot Phase

StatusCompleted
PhaseNot applicable
Started
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Record History

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  1. Minor Trial completed
    • Eligibility criteria expanded, about 10 words
    • Secondary endpoints: details revised at 6 of 14 entries
  2. Minor Study completion date: Apr 2026 to Jun 16, 2026v6
  3. Minor Primary completion date changed from estimate of Jul 2024 to Jul 23, 2024v5
  4. Minor Trial status: Recruiting to Active, Not Recruitingv4 Show 4 more changesShow less
    • Enrollment target: estimated 6 to confirmed 9
    • Primary completion date: Apr 2024 to Jul 2024
    • Study completion date: Jul 2027 to Apr 2026
    • Site details revised
  5. Notable Trial status: Not Yet Recruiting to Recruitingv3 Show 4 more changesShow less
    • Primary completion date: Feb 2024 to Apr 2024
    • Study completion date: Dec 2025 to Jul 2027
    • Start date changed from estimate of Aug 2023 to Sep 12, 2023
    • Site details revised
  6. Notable Start date: Feb 2023 to Aug 2023
    • Primary completion date: Nov 2023 to Feb 2024
    • Study completion date: May 2025 to Dec 2025
    v2
  7. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Shoulder pain is one of the most commonly reported musculoskeletal complaints, which negatively affects upper limb use, night rest, daily life activities, work, sports performance and autonomy. Rotator cuff disease represents the most common cause of shoulder pain and it is responsible for up to 70% of all shoulder related visits to clinicians. Its incidence furthermore is expected to grow as the population ages. A wide range of conditions are included under the umbrella term of rotator cuff disease, including rotator cuff tendinopathy, subacromial bursal pathology, and partial-thickness or full-thickness rotator cuff tears (RCTs). The latter ones, i.e. rotator cuff tears, form the indications for which the test devices, the SINEFIX implant and instruments, are intended. Despite the high prevalence of this condition, the pathophysiology and healing potential are not well understood, making the condition challenging to predictably treat in some patient populations. RCTs may occur in young people as a consequence of trauma (e.g. acute shoulder dislocation), however RCTs typically present in middle-aged or elderly people and cannot always be attributed to precipitating events or trauma. Instead, they can be attributed to degenerative processes, and are therefore referred to as degenerative RCTs. For RCTs, treatment options include both surgical and non-surgical (conservative) procedures. In this context, the SINEFIX implant and instruments were developed to treat adult patients with rotator cuff lesions of size up to 2 cm through arthroscopic reconstruction.
Trial Details
NCT Number NCT05721560
Lead Sponsor BAAT Medical Products B.V.
Conditions
(from sponsor)
Rotator Cuff Tears (RCTs)
Related terms Rotator Cuff Injuries
Enrollment 9 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov