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Tennis ElbowPhase 2NCT06171555

Efficacy of CTM for Tennis ELbow

A Phase 2 study testing CTM and Celestone in people with Tennis Elbow and Lateral Epicondylitis \(Tennis Elbow\), run by Indiana Hand to Shoulder Center at 1 site in United States.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

In this study, the objective is to evaluate the effectiveness of a single application of human Connective Tissue Allograft (CTA) as a treatment of LET. CTM Biomedical markets and distributes decellularized particulate human placental connective-tissue matrix products, intended solely for homologous use to supplement… Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
CTM and Celestone
Could I receive a placebo?
No, everyone receives an active treatment
How many people
54 participants
Where
1 siteUnited States
Study dates
26 Jan 2023to 31 Dec 2025
Phase
Phase 2
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 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Males or females age 18 or older
  • Patients presenting with symptomatic lateral epicondylitis for at least 6 weeks
  • Patients who have not had a meaningful symptomatic improvement after 6 weeks of physical therapy
  • Patients who can consent to be a part of this study
  • Patients who are able to return to the Indiana Hand to Shoulder Center or a satellite location for follow up time points

Who cannot join

  • Previous surgery to the lateral side of the elbow
  • Systemic inflammatory conditions (RA, psoriatic arthritis, lupus, etc)
  • Previous elbow injection within the last 6 months
  • History of recent elbow trauma
  • Patients actively involved in workman's compensation cases
  • Non-English Speaking Patients

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Indiana Hand to Shoulder Center

    Indianapolis, Indiana, 46260

Other trials in United States

About this study

Official title: Efficacy of Connective Tissue Allograft Versus Steroid Injections in Treatment of Lateral Epicondylitis

In this study, the objective is to evaluate the effectiveness of a single application of human Connective Tissue Allograft (CTA) as a treatment of LET. CTM Biomedical markets and distributes decellularized particulate human placental connective-tissue matrix products, intended solely for homologous use to supplement or replace damaged or inadequate connective-tissue. These are structural tissue allografts processed according to the criteria contained in 21CFR 1271.10(a) for regulation solely under section 361 of the Public Health Service Act. Drug/Device Handling: If the research involves drugs or device, describe your plans to store, handle, and administer those drugs or devices so that they will be used only on subjects and be used only by authorized investigators.

Read the detailed description

Lateral Elbow Tendinopathy (LET) is considered an overload injury of the extensor tendons of the forearm where they attach at the lateral epicondyle. LET is a common condition encountered both in primary care and specialty clinics. A population-based study reported an incidence of 3.4 (95% CI, 3.3-3.5) per 1000. The highest incidence was among individuals aged 40 to 49 years, with 7.8 per 1000 in male patients and 10.2 per 1000 in female patients. Work restrictions were reported in 16% of the patients, and 4% reported missing 1 to 12 weeks of work. The recurrence rate within 2 years was 8.5% and remained constant over time. The study data suggest that patients without resolution after 6 months of onset may have a prolonged disease course and may need surgical intervention. The patient demographic is typically active in the workforce and LET related absenteeism results in a substantial economic impact. Pain relief, timely return to work, and avoidance of surgical intervention are therefore important LET treatment goals. Patients suffering from LET are grouped into 2 entities: Group 1 experience symptoms in an acute (tendinitis) phase that is largely influenced by the local inflammation stemming from over-use activities. Group 2 developed tendon degeneration and/or bony responses due to a persistent, chronic (tendinosis) pathology. Histologic specimens from chronic cases confirm that tendinosis is not an acute inflammatory condition but rather a failure of the normal tendon repair mechanism associated with angio-fibroblastic degeneration. The cause of elbow tendinosis is most likely a combination of mechanical overloading and abnormal microvascular responses. Further research into the precise cause of tendinosis is, however, still needed. The chief complaint in both groups is elbow pain with or without activity. Numerous methods have been advocated for treating LET including rest, nonsteroidal anti-inflammatory medication, bracing, physical therapy, iontophoresis, extracorporeal shock wave therapy, and botulism toxin. Injections of corticosteroids or whole blood, and various types of surgical procedures have also been recommended. The utility of several of these treatments has recently come into question. For example, one recent report noted that there is no difference between using corticosteroid or local anesthetic when treating elbow tendinosis with an injection. A recent review of common growth factors suggested human CTA may be useful for tendon and ligament healing in vivo.

The primary study endpoint is based on the hypothesis that treatment of LET with a single application of CTA will provide a clinically meaningful improvement of the Patient-Related Tennis Elbow Evaluation (PRTEE) Pain Subscale Secondary endpoints include VAS pain and elbow range of motion. Secondary endpoints also include PROMIS scores of pain interference and depression. A single assessment numerical evaluation (SANE) of elbow function will also be obtained.

Being tested
CTM, Celestone
Medical subject headings
Tennis Elbow

What participants receive

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

  • CTMDevice

    Also called Connective Tissue Matrix

    decellularized particulate human placental connective-tissue matrix products, intended solely for homologous use to supplement or replace damaged or inadequate connective-tissue. These are structural tissue allografts processed according to the criteria contained in 21CFR 1271.10(a) for regulation solely under section 361 of the Public Health Service Act.

  • CelestoneDrug

    Also called Corticosteroid

    standard of care

Study groups in NCT06171555
Study groupRoleWhat they receive
Standard of Care Steroid InjectionActive comparatorGroup 1 Control Group: standard corticosteroid injection: 1cc of celestone (6mg) diluted with 1 cc of 1% lidocaine and inject at the ECRB origin at area of maximal pain when palpated.
Receives: Drug: Celestone
Test CTM InjectionExperimentalGroup 2 Test Group: CTM injection: 1cc of CTM Boost will be diluted with 1 cc of 1% lidocaine and injected at the ECRB origin at area of maximal pain when palpated. CTM Boost is a connective tissue matrix suspended in saline. (injection will need to be with a 23 gauge needle and 3 cc syringe)
Receives: Device: CTM

What is being measured

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

  1. Patient-Related Tennis Elbow Evaluation (PRTEE) Pain Subscale

    PROM

    Measured: 6 Months

Secondary outcomes (5)
  1. VAS Pain

    pain

    Measured: 6 Months

  2. PROMIS Pain Interference

    PROM

    Measured: 6 Months

  3. PROMIS Depression

    PROM

    Measured: 6 Months

  4. Grip Strength

    grip strength taken with a calibrated jamar instrument

    Measured: 6 Months

  5. Range of Motion

    wrist range of motion measured with a goniometer with elbow both flexed and extended

    Measured: 6 Months

Timeline

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

  1. First posted14 Dec 2023
  2. Study start26 Jan 2023
  3. Primary completion31 Dec 2025 (estimated)
  4. Study completion31 Dec 2025 (estimated)

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 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Group 1 Control Group: standard corticosteroid injection: 1cc of celestone (6mg) diluted with 1 cc of 1% lidocaine and inject at the ECRB origin at area of maximal pain when palpated. Group 2 Test Group: CTM injection: 1cc of CTM Boost will be diluted with 1 cc of 1% lidocaine and injected at the ECRB origin at area of maximal pain when palpated. CTM Boost is a connective tissue matrix suspended in saline. (injection will need to be with a 23 gauge needle and 3 cc syringe) Randomization will be through a computerized random allocation assigned by the Research Coordinator on the day of consent.
Masking
Single blind
Who is masked
Participant
Enrolment
54 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06171555
Sponsor's protocol ID
IHTSC CTM Project HC22-1
Status last verified
Dec 2023
First submitted
30 Nov 2023
Last updated
27 Mar 2024
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 Phase 2 study testing CTM and Celestone in people with Tennis Elbow and Lateral Epicondylitis \(Tennis Elbow\), run by Indiana Hand to Shoulder Center 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 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: status not confirmed, as of the sponsor's last update on 27 Mar 2024. 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.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Results are not available in the source record.

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?

Patient-Related Tennis Elbow Evaluation (PRTEE) Pain Subscale (time frame: 6 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 27 Mar 2024.

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