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Rotator Cuff TearsNCT04361266

Use of Nanoscaffold Augmentation in Rotator Cuff Repair: Clinical Outcome and Ultrasound Assessment of Healing Rates and Vascularity

A study testing Rotium nanoscaffold in people with Rotator Cuff Tears and Rotator Cuff Injuries, run by Joshua Szabo, MD.

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record
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Trial summary

The purpose is to assess Rotium, a novel nanoscaffold, impact on healing of a repaired rotator cuff and compare to a repair without Rotium. Animal (sheep) models have shown both quicker and more organized healing when Rotium is used, but there are no studies to confirm these outcomes translate to human population. Read more about this study

Who is it for?
Ages 18 to 80 years
What is being tested?
Rotium nanoscaffold
Could I receive a placebo?
No, everyone receives an active treatment
How many people
0 participants
Where
No sites listed yet
Study dates
1 Aug 2022to 1 Nov 2023
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • -symptomatic supraspinatus or supraspinatus and infraspinatus tear that can be repaired to the greater tuberosity in an anatomical manner using a dual layer repair technique.
  • also included will be patients that have concomitant pathology addressed at time of surgery, specifically pathologies of the biceps tendon (tenodesis or tenotomy), arthrosis of the acromioclavicular joint (distal clavicle resection), or labral tearing (debridement or repair)
  • included age range of subjects will be from 18-80 years old

Who cannot join

  • diabetes, cancer or medical states that may impair healing, such as organ transplantation or systemic inflammatory process treated with immune modulating drugs (chemotherapy, immunosuppression drugs)
  • prior surgery to the ipsilateral rotator cuff tendon
  • need of soft tissue releases to accomplish an anatomic repair, partial repairs and/or concomitant subscapularis repair
  • significant glenohumeral arthritis
  • active or ongoing infection
  • pregnancy

About this study

The purpose is to assess Rotium, a novel nanoscaffold, impact on healing of a repaired rotator cuff and compare to a repair without Rotium. Animal (sheep) models have shown both quicker and more organized healing when Rotium is used, but there are no studies to confirm these outcomes translate to human population.

Hypothesis: Rotium rotator cuff repairs will heal both quicker and better than traditional rotator cuff repair techniques.

Read the detailed description

Patients indicated for rotator cuff repair surgery will be offered participation within the study and consented accordingly. A copy of the consent will be provided to the participant. A preoperative ultrasonographic assessment will occur by Dr. Onishi. A randomization process by computer program will determine patients who have Rotium augmented repairs, or not. The patients will not be blinded.

The surgery will be carried out by a single surgeon making all aspects uniform, except if there is or is not a Rotium patch. The Rotium patch will be implanted in accordance to standards of handling sterile implants and placed in a manner that is consistent to its FDA approval. The patch will be furnished by the institution where the surgery is being performed. Digital photography will document pertinent arthroscopic operative findings per standard of care.

Participant assessment will commence preoperatively in an outpatient clinic then continue in postoperative period, occurring at 2, 4, 6 weeks and 3, 6 and 12 month intervals. During each visit, the participants will be assessed by two clinicians: the principal investigator and a blinded ultrasonographer.

Preoperative assessment will include obtaining baseline patient reported outcomes (UCLA, Rowe, Constant, American Shoulder and Elbow Surgeons (ASES) score and SANE (Single Alpha Numeric Evaluation)scores) by paper questionnaire. A medical history will document NSAID use, cortisone injections about the shoulder, tobacco usage, narcotic medicine consumption, and pregnancy status. Due to their deleterious effects on healing, all patients will be instructed to not take NSAIDs in the first 6 weeks postoperative. Noncompliance will be noted, but not disqualify the participant from study. Smoking cessation will be strongly encouraged. A shoulder physical examination will be performed; specifically range of motion assessment in multiple planes (frontal flexion, internal and external rotation at 90 degrees of abduction and at side), rotator cuff muscle strength testing with the scapula stabilized, scapula posture observed, and provocative tests for impingement syndrome. Medical records will be reviewed. This evaluation will be performed by the principal investigator and will take 45-60 minutes. The participant will undergo a separate diagnostic ultrasonographic assessment of the rotator cuff tendons by blinded ultrasonographer. This will take 15-30 minutes.

Aftercare of each population will be identical and will include a 6-week period of sling immobilization, brief perioperative narcotic medicine, and physical therapy. Physical therapy protocols will be identical. The participants will be treated by a variety of physical therapists. All physical therapy will occur out of the home at a PT clinic. Additional home exercises will be furnished and will be independently performed by the participants.

Specifically, at the 2-week postoperative visit a history will be obtained to quantify narcotic usage, NSAID usage, VAS pain score, and assess for any complications. The surgical site and sling will be inspected, passive range of motion of the shoulder assessed (frontal flexion and external rotation at the side), and the examine will exclude any complications. Physical therapy for shoulder passive range of motion and periscapular strengthening will be prescribed, home exercise sheet provided, and the abduction portion of the sling will be discontinued. Shoulder radiographs will be performed. This visit will take 15-30 minutes. In addition and separate to this,blinded ultrasonographer will perform ultrasound assessment of the repaired rotator cuff. Vascularity using superb microvascular imaging and standard ultrasound techniques will assess vascularity and rotator cuff repair integrity. If possible, elastography will be performed. These images will be stored in de-identified manner within University of Pittsburgh HIPPA-compliant cloud. This will take 15-30 minutes and may be done at a separate time.

At the 4-week postoperative visit a history will be obtained to quantify narcotic usage, NSAID usage, pain score, and assess for any complications. The surgical site and sling will be inspected, passive range of motion of the shoulder (frontal flexion and external rotation at the side) assessed, and the examine will exclude any complications. The prior physical therapy and home exercises will be continued. This visit will take 15-30 minutes. In addition and separate to this, blinded ultrasonographer will perform ultrasound assessment of the repaired rotator cuff. This will take 15-30 minutes and may be done at a separate time.

At the 6-week postoperative visit a history will be obtained to quantify narcotic usage, NSAID usage, pain score, and assess for any complications. The surgical site and sling will be inspected, passive range of motion of the shoulder (frontal flexion, internal and external rotation at 90 degrees of abduction and at side) assessed, and the examine will exclude any complications. The sling will be discontinued and new physical therapy and home exercises will be provided; therapy will include shoulder passive range of motion and periscapular strengthening and include rotator cuff strengthening progressing from isometric to concentric then to eccentric with the pace being determined by a physical therapist, but done in a pain free manner. Additionally, patient reported outcomes (UCLA, Rowe, Constant, ASES and SANE scores) will be collected. This visit will take 30-45 minutes. In addition and separate to this, blinded ultrasonographer will perform ultrasound assessment of the repaired rotator cuff. This will take 15-30 minutes and may be done at a separate time.

At the 3-, 6- and 12-month postoperative visits a history will be obtained to assess shoulder functionality/limitations, quantify NSAID usage, pain score, and assess for any complications. The examination will be similar to the 6-week evaluation, except rotator cuff specific strength will be assessed similar to the preoperative testing. Necessity of ongoing physical therapy will be considered and ordered appropriately. Home exercises will be continued. These visits will take 30-45 minutes. In addition and separate to this, blinded ultrasonographer will perform ultrasound assessment of the repaired rotator cuff. This will take 15-30 minutes and may be done at a separate time.

Being tested
Rotium nanoscaffold, Control arm rotator cuff repair
Medical subject headings
Rotator Cuff Injuries

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Rotium nanoscaffoldDevice

    Rotium bioabsorbable nanoscaffold placed between bone-tendon interface of rotator cuff repair construct

  • Control arm rotator cuff repairProcedure or surgery

    Standard rotator cuff repair without Rotium

Study groups in NCT04361266
Study groupRoleWhat they receive
Rotium patch recipientExperimentalSubjects with Rotium nano scaffold patch included in rotator cuff repair construct
Receives: Device: Rotium nanoscaffold
ControlActive comparatorSubjects undergoing non-patch augmented rotator cuff repair
Receives: Procedure: Control arm rotator cuff repair

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Rotator cuff integrity baseline/preoperative

    ultrasound assessment of rotator cuff

    Measured: preoperative

  2. Rotator cuff repair integrity @ 2 weeks

    ultrasound assessment of rotator cuff

    Measured: postoperative at 2 weeks

  3. Rotator cuff repair integrity @ 4 weeks

    ultrasound assessment of rotator cuff

    Measured: postoperative at 4 weeks

  4. Rotator cuff repair integrity @ 6 weeks

    ultrasound assessment of rotator cuff

    Measured: postoperative at 6 weeks

  5. Rotator cuff repair integrity @ 3 months

    ultrasound assessment of rotator cuff

    Measured: postoperative 3 months

  6. Rotator cuff repair integrity @ 6 months

    ultrasound assessment of rotator cuff

    Measured: postoperative at 6 months

  7. Rotator cuff repair integrity @ 12 months

    ultrasound assessment of rotator cuff

    Measured: postoperative at 12 months

  8. Postoperative rotator cuff vascularity during healing

    ultrasound assessment of rotator cuff at repair site using superb microvascular imaging (SMI)

    Measured: postoperative at 2 weeks

  9. Postoperative rotator cuff vascularity during healing

    ultrasound assessment of rotator cuff at repair site using superb microvascular imaging (SMI)

    Measured: postoperative at 4 weeks

  10. Postoperative rotator cuff vascularity during healing

    ultrasound assessment of rotator cuff at repair site using superb microvascular imaging (SMI)

    Measured: postoperative at 6 weeks

  11. Postoperative rotator cuff vascularity during healing

    ultrasound assessment of rotator cuff at repair site using superb microvascular imaging (SMI)

    Measured: postoperative at 3 months

  12. Postoperative rotator cuff vascularity during healing

    ultrasound assessment of rotator cuff at repair site using superb microvascular imaging (SMI)

    Measured: postoperative at 6 months

  13. Postoperative rotator cuff vascularity during healing

    ultrasound assessment of rotator cuff at repair site using superb microvascular imaging (SMI)

    Measured: postoperative at 12 months

Secondary outcomes (5)
  1. University California Los Angeles Shoulder score

    Outcome score

    Measured: preoperative and postoperative at 6 weeks and 3,6,12 months postoperative

  2. Rowe score

    Outcome score

    Measured: preoperative and postoperative at 6 weeks and 3,6,12 months postoperative

  3. Constant score

    Outcome score

    Measured: preoperative and postoperative at 6 weeks and 3,6,12 months postoperative

  4. American shoulder and elbow surgeons score

    Outcome score

    Measured: preoperative and postoperative at 6 weeks and 3,6,12 months postoperative

  5. SANE score

    Outcome score

    Measured: preoperative and postoperative at 2,4, 6 weeks and 3,6,12 months postoperative

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Apr 2020
  2. Study start1 Aug 2022 (estimated)
  3. Primary completion1 Aug 2023 (estimated)
  4. Study completion1 Nov 2023 (estimated)

Why it stopped: withdrawn

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
prospective randomized control trial
Masking
Single blind
Who is masked
Investigator
Enrolment
0 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04361266
Sponsor's protocol ID
STUDY19080165
Status last verified
Oct 2022
First submitted
17 Apr 2020
Last updated
18 Oct 2022
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: There is no plan to share data at this time.

Questions about this trial

What is this clinical trial studying?

A study testing Rotium nanoscaffold in people with Rotator Cuff Tears and Rotator Cuff Injuries, run by Joshua Szabo, MD.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: withdrawn, as of the sponsor's last update on 18 Oct 2022. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was withdrawn before enrolling participants, so there are no results.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Rotator cuff integrity baseline/preoperative (time frame: preoperative). The study lists 13 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Oct 2022.

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