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Rotator Cuff TearNCT03001050

Rotator Cuff: Does the Vascularity Matter and the Role for PINPOINT

A study testing PINPOINT System in people with Rotator Cuff Tear, run by Nirav Amin, MD at 1 site in United States.

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record
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Trial summary

The overall goal of doing this study is to improve long term patient function and outcomes in the healing rates of Rotator Cuffs. The investigators would also like to see if this method can be more cost effective and time efficient for Rotator Cuff evaluation during arthroscopy. Read more about this study

Who is it for?
Ages 30 to 80 years
Conditions the study is for
Rotator Cuff Tear
What is being tested?
PINPOINT System
Could I receive a placebo?
No, everyone receives an active treatment
How many people
0 participants
Where
1 siteUnited States
Study dates
20 Dec 2017to 20 Dec 2017
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 30 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Diagnosis of requiring Rotator Cuff repair surgical treatment
  • Willingness and ability to comply with the requirements of the protocol including follow-up requirements.
  • Willing and able to sign a study specific informed consent form to participate.
  • Age range of ≥ 30 years old and ≤ 80 years old at time of surgery.
  • Male or female.

Who cannot join

  • Previous Rotator cuff repair or shoulder surgery.
  • Active systemic infection or infection at the operative site.
  • Co-morbid medical conditions of the upper extremities that may affect the neurological and/or pain assessment.
  • History of an osteoporotic fracture.
  • History of an endocrine or metabolic disorder (e.g., Paget's disease) known to affect bone and mineral metabolism.
  • Taking medications that may interfere with bony/soft tissue healing including chronic steroid use.
Show all 11Show fewer
  • Rheumatoid arthritis or other autoimmune disease or a systemic disorder such as HIV, active hepatitis B or C or fibromyalgia.
  • Insulin-dependent type 1 or type 2 diabetes.
  • Medical condition (e.g., unstable cardiac disease, cancer) that may result in patient death or have an effect on outcomes prior to study completion.
  • Pregnant, or intend to become pregnant, during the course of the study.
  • Severe obesity (Body Mass Index > 40).

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Loma Linda University Health, Department of Orthopaedic Surgery

    Loma Linda, California, 92354

Other trials in United States

About this study

The overall goal of doing this study is to improve long term patient function and outcomes in the healing rates of Rotator Cuffs. The investigators would also like to see if this method can be more cost effective and time efficient for Rotator Cuff evaluation during arthroscopy.

Read the detailed description

Background or rationale for this study:

4.5 million Patient's seek medical care for shoulder pain annually in the United States.

250,000 patients receive rotator cuff surgery in the United States annually. Those rotator cuff surgeries produce a societal savings of $3.44 billion per year; averaging $13,771.00 per patient younger than age 61. In which case rotator cuff tears Increases with age.

The Societal and Economic Value of Rotator Cuff Repair (AAOS) 2015 Rotator cuff repairs result in a lifetime societal savings in the U.S. of approximately $3.44 billion annually. Societal savings offset the direct costs of treatment in patients younger than age 61, resulting in an average net savings of $13,771 per patient. This number significantly increased to $77,662.00 for patients younger than 40 years of age.

Common problem, a 55 year-old man injured his left arm. He uses a sling and has difficulties performing simple activities. 1 week later he falls develops immediate pain in his shoulder. On examination he is unable to move his left arm in any upward or sideways direction without supporting it with his other arm. Radiographs he brought show no signs of shoulder osteoarthritis, dislocation, or fracture.

Shoulder pain is the third most common musculoskeletal reason for seeking medical care. Although smaller tears are less likely to propagate, larger tears tend to progress with time and eventually may become irreparable because of significant tendon retraction, muscle atrophy, or both or when the tendons tissue quality does not allow repair.

In 1972-Neer proposed that 95% of rotator cuff injuries were caused by mechanical compression under the coracoacromial arch, others argued cuff tear caused spur formation.

  • Type I-flat
  • Type II-curved
  • Type III-hooked

Multifactorial:

Extrinsic factors;

  • Subacromial impingement
  • Glenohumeral instability
  • Internal impingement
  • Trauma (acute/repetitive) Intrinsic Factors;
  • Tendon vascular supply
  • Collagen fiber abnormalities

A positive painful arc test result and positive external rotation resistance test result were the most accurate finding for detecting Rotator Cuff Disease; whereas the presence of a positive lag tests (external or internal rotation) result was most accurate for diagnosis of a full-thickness rotator cuff tear. Differentiating a full thickness tear from a partial tear, the most sensitive test was the belly-press test (56.8%), and the most specific was the lift-off test (96.95).

Bone microvascularization of the footprint plays a role in rotator Cuff healing. The use of the Pinpoint may play a pivotal role in rotator Cuff healing, en lieu of Plasma Rich platelets with variable results based on concentration levels.

6 level randomized controlled trials showed no clinically significant differences in Constant scores, University of California, Los Angles shoulder rating (UCLA), and American Shoulder and Elbow Surgeons (ASES) scores between double-row and single-row rotator cuff repair. Overall odds ratio (OR) of intact rotator cuff tendon healing was 1.93 in patients treated with double-row versus single-row repair, and the difference was significant.

A statistically significant benefit of double-row repair in the ASES and UCLA scores was observed in the subgroup with tears greater than 3cm. The take home point; Double row may improve structural healing: Clinical Relevance?

9 studies in the meta-analysis, 5 of which were randomized prospective studies (LEVEL1).

Double-row rotator cuff repair techniques have a significantly lower re-tear rate, higher ASES score and greater range of motion of internal rotation compared with single-row repair techniques. Point: Especially in those rotator cuff tears with a size >30mm, the double-row technique is recommended for repair.

This was a Level 4 study out of the Cleveland Clinic which showed the majority of the tears occurred between 6 and 24 weeks. The role of a potential hand held device can assess the tendon quality in the office and change the rehab protocols based on tendon retraction.

Role for study interventions:

  • Assessing the bony vascularity at the footprint and the tendon integrity.
  • Current standard of care:

Steroid injection as a non-operatively treatment option. Could the steroid injections be affecting the tendon micro vascularization? Could using the Pinpoint assess tendon quality and long term healing a potential.

  • Cystic osseous resorption and osteolysis.
  • Breakdown products (PLLA) cause synovitis and chondrolysis.
  • Breakdown products (PLLA) may interfere with healing-Complications of Bioabsorbable Suture anchors in the shoulder.

Why Medical Row Knots?

  • Enhances Biology be sealing footprint from synovial fluid.
  • Compared to knotless medical row, better biomechanics incl. load to failure, stiffness, less gap formation.
  • A biomechanical comparison of 2 technical of double-row rotator cuff fixation: the importance of medical row knots.

Clinical Implications and Surgeon's Role;

  • Choice of a tissue-penetrating instrument; smaller penetrating devices resulting in improves characteristics of stitch holding strength.
  • Size of the tissue bite; bigger bite size being stronger.
  • Most critical variable under a surgeons control during a rotator cuff repair is the choice of the stitch.

Role for Pinpoint:

In the re-tear and partial-repair groups, postoperative tendon preservation at the middle fact significantly affected the Japanese Orthopaedic Assocation (JOA) and UCLA scores (P=.014, respectively). Considering the patients with tendon healing had better clinical factors, the Pinpoint may help identify the tendon and footprint vascularity at time of surgery.

Goals for the Pinpoint:

To attempt to show that increased vascularity may have an effect of the muscle quality, therefore improving the strength and function long term.

Objective:

  • This prospective study aims to obtain the accurate level within a range of a 95% CI imaging Rotator Cuff tendons and the footprint.
  • Ensure the Vascularity of the tendon after the footprint and the tendon have been restored to the anatomic footprint. See if the level of the Rotator Cuff bite affects the vascular flow of the tendon.
  • Does tying the medical row or excessive tension change the vascularity of the Rotator Cuff.
  • We would like to see if by using the Pinpoint system it may be more cost effective then Plasma Rich Platelet.
  • Decrease the number of the re-tear rates in Rotator cuff repairs.

Overall goals: Improve long term patient function and outcomes. Increase Rotator Cuff healing rates. Cost effective and time efficient method of Rotator Cuff evaluation during arthroscopy.

Procedures involved (Research Interventions)

Patients undergoing a Rotator Cuff Repair:

  • Pre-operatively Questioners to be completed at pre-op American Shoulder and Elbow Surgeons (ASES), University California Los Angeles (UCLA), Disabilities of the arm, shoulder and hand (DASH), Short Form Health Survey-12 (SF-12) \& Short Form Health Survey-36 (SF-36)
  • Operative Collect OR information
  • Post-operative ASES, UCLA, DASH SF-12 \& SF-36
  • Ultra sounds 3 months, 6 months, 1 year and 24 months

The operative intervention will proceed as current standard protocol dictates for the described procedure. No changes in the operative technique will be undertaken apart from injection of the dye and visualization with the camera. The idea would be to place the Pinpoint probe within the subacrominal space, to check the vascular status of the tendon, and then take a bite of the tendon and place the pinpoint back to check if the vascularity has decreased. The Indocyanin Green dye kit will be used along with the PINPOINT system . Patients with potential allergies or a history of allergies or sensitivity to sodium iodide or iodinated contrast agents should not use this system, and will not be asked to participate. The possible adverse reactions are, anaphylaxis, Hypotension, tachycardia, dyspnea and urticarial. The duration of the procedure will be increased because of the study imaging; this could be 15 to 30 minutes.

Being tested
PINPOINT System
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.

  • PINPOINT SystemDevice

    To use the camera probe and identify the tendon and footprint vascularity at the time of surgery

Study groups in NCT03001050
Study groupRoleWhat they receive
PINPOINT systemOtherThe operative intervention will proceed as current standard protocol dictates for the described procedure. No changes in the operative technique will be undertaken apart from injection of the dye and visualization with the camera. The idea would be to place the Pinpoint probe within the subacromial space, to check the vascular status of the tendon, and then take a bite of the tendon and place the pinpoint back to check if the vascularity has decreased. The Indocyanine Green dye kit will be used along with the PINPOINT system .
Receives: Device: PINPOINT System

What is being measured

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

  1. PINPOINT System-ASES

    American Shoulder and Elbow Surgeons questionnaire this will be used for scoring

    Measured: Change from baseline at 24 months

Secondary outcomes (4)
  1. PINPOINT System-UCLA

    University California Los Angeles, shoulder rating scale

    Measured: Change from baseline at 24 months

  2. PINPOINT System-DASH

    Disabilities of the arm, shoulder and hand scores

    Measured: Change from baseline at 24 months

  3. PINPOINT System-SF-36

    The short form heath survey with 36 questions to measure health status

    Measured: Change from baseline at 24 months

  4. PINPOINT System-SF-12

    Short Form Health Survey with 12 questions to measure mental and physical status

    Measured: Change from baseline at 24 months

Timeline

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

  1. First posted22 Dec 2016 (estimated)
  2. Study start20 Dec 2017
  3. Primary completion20 Dec 2017
  4. Study completion20 Dec 2017

Why it stopped: Investigator requested to close, lack of equipment available.

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
Diagnosis
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
0 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03001050
Sponsor's protocol ID
5160379
Status last verified
Feb 2018
First submitted
5 Dec 2016
Last updated
26 Feb 2018
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing PINPOINT System in people with Rotator Cuff Tear, run by Nirav Amin, MD at 1 site in United States.

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 5 inclusion and 11 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 26 Feb 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

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?

PINPOINT System-ASES (time frame: Change from baseline at 24 months). 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 26 Feb 2018.

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