Efficacy of a Single Image Guided Injection of CTM for Glenohumeral Arthritis

Phase 1

Active, not recruiting

• Conditions: Osteoarthritis Shoulder; Shoulder Osteoarthritis; Glenohumeral Osteoarthritis
• Interventions: Device: CTM Injection

• Registration Number: NCT06171542
• Lead Sponsor: Indiana Hand to Shoulder Center

Brief Summary

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.

The goal of this study is to determine the success rate of a single, image guided glenohumeral CTM injection (for radiographically confirmed glenohumeral osteoarthritis at follow up intervals of 1, 2, 3, 4, 6, 9, and 12 months. This will be measured using the Likert Pain Scale (LPS) and Oxford Shoulder Score (OSS). Secondary goals are to identify if certain demographic or imaging factors exist that predict early symptom recurrence requiring additional intervention, defined as a second connective tissue matrix injection, a subsequent corticosteroid injection, or arthroplasty.

Detailed Description

A recent prospective study by our center identified a clinically meaningful and statistical improvement after corticosteroid injection in the Oxford Shoulder Score and VAS pain scores in patients with glenohumeral arthritis2.

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. CTM Flow is decellularized particulate human placental connective-tissue matrix provided in a vial.

Osteoarthritis creates pain due to damaged tissues. CTM has been approved to supplement and replace damaged tissues. It is not replacing the damaged cartilage with new cartilage, but rather with other connective tissues. Previous unpublished studies in tonsil surgery and knee arthritis surgery have shown improvement from the CTM injections.

Image guided injection of the glenohumeral joint has been shown to be more accurate than blind in-office injections and will thus be used in this study3.

The goal of this study is to determine the success rate of a single, image guided glenohumeral (GH) CTM injection (for radiographically confirmed glenohumeral osteoarthritis at follow up intervals of 1, 2, 3, 4, 6, 9, and 12 months. This will be measured using the Likert Pain Scale (LPS) and Oxford Shoulder Score (OSS). Secondary goals are to identify if certain demographic or imaging factors exist that predict early symptom recurrence requiring additional intervention, defined as a second connective tissue matrix injection, a subsequent corticosteroid injection, or arthroplasty.

Study Timeline

• Study Start: 2022-12-22
• Status Verified: 2023-12
• Study First Submitted: 2023-12-01
• Study First Submitted QC: 2023-12-06
• Study First Posted: 2023-12-14
• Last Update Submitted: 2024-03-26
• Last Update Posted: 2024-03-27
• Primary Completion: 2024-04-30
• Study Completion: 2025-04-30

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

1. Radiographic documented Glenohumeral osteoarthritis (grade 1-3)
2. Males or females age 18 or older
3. Patients receiving a CTM injection for their initial treatment
4. Patients who can consent to be a part of this study
5. Patients who are able keep up regular communication through phone calls or electronic PROs

Exclusion Criteria

1. Inflammatory Arthritis
2. Brachial Plexopathy
3. Cervical spine abnormalities such as radiculopathies
4. age less than 18 years
5. those unable to keep up monthly communication through phone calls and/or electronic PROs
6. Absence of glenohumeral osteoarthritis
7. Pregnancy or breastfeeding
8. Non-english speaking

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
CTM Shoulder Injection	CTM Injection	-

Primary Outcome Measures

Name	Time	Method
Likert Pain Scale	12 Months	PROM
Oxford Shoulder Score	12 Months	PROM

Trial Locations

Locations (1)

Indiana Hand to Shoulder Center; 🇺🇸 Indianapolis, Indiana, United States