Postmarketing Multicenter Study of Intra-Articular DIART ONE / EASYGO ONE for Knee Osteoarthritis

NCT ID: NCT06927934

Last Updated: 2025-04-15

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 55 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2021-08-14
• Study Completion Date: 2022-06-27

Brief Summary

This study looked at how safe and effective a hyaluronic acid-based injection (called DIART ONE or EASYGO ONE) is for people with knee osteoarthritis. The injection helps replace the natural fluid in the knee joint to reduce pain and improve movement. Patients received one injection, and their symptoms were tracked over 6 months using phone calls and clinic visits. The goal was to see how much pain and joint function improved, and to check for any side effects.

Detailed Description

This was a post-marketing, observational clinical study designed to evaluate the safety, tolerability, and effectiveness of a single intra-articular injection of a stabilized hyaluronic acid-based medical device, marketed under the names DIART ONE (in Ukraine) and EASYGO ONE (in Poland). The study focused on adults diagnosed with knee osteoarthritis, a common joint disease that causes pain, stiffness, and reduced mobility due to the breakdown of joint cartilage and decreased synovial fluid.

A total of 55 participants were enrolled across multiple centers. Each participant received one injection of the investigational product into the affected knee. The specific formulation (either 20 mg/mL - 2 mL or 30 mg/mL - 3 mL) was selected by the treating physician based on clinical needs and product availability.

The primary goal of the study was to assess the change in pain levels 3 months after injection, using the WOMAC (Western Ontario and McMaster Universities Osteoarthritis Index) pain subscale, a validated questionnaire used to evaluate joint pain. Secondary outcomes included changes in pain at other time points (1, 2, 4, 5, and 6 months), as well as changes in joint stiffness and physical function.

Participants were monitored over a 6-month period through a mix of in-person and phone follow-ups. Adverse events, including any side effects related to the product or injection, were documented and analyzed.

Conditions

Knee Osteoarthritis; Osteoarthritis of the Knee; Degenerative Joint Disease

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: RETROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• Age ≥ 21 years.
• Body Mass Index (BMI) ≥ 18.5 kg/m².
• Body Mass Index (BMI) < 35 kg/m².
• Presence of trauma or degenerative diseases (e.g., osteoarthritis) confirmed by radiographic imaging (Kellgren-Lawrence score 2-4).
• The subject is prescribed an injection of stabilized hyaluronic acid (DIART ONE 20 mg/mL - 2 mL or 30 mg/mL - 3 mL) for temporary replacement of synovial fluid in the knee joint.
• Signed written informed consent to participate in the study.

Exclusion Criteria

• Age < 21 years.
• Body Mass Index (BMI) < 18.5 kg/m².
• Body Mass Index (BMI) ≥ 35 kg/m².
• Pregnancy or lactation.
• No radiographic confirmation of osteoarthritis (Kellgren-Lawrence score 0-1).
• Known hypersensitivity to hyaluronic acid, its metabolites, or excipients in the injectable implant.
• Increased bleeding tendency.
• Injury or infection at the injection site.
• Confirmed infectious joint disease.
• Systemic connective tissue diseases (e.g., active rheumatoid arthritis, ankylosing spondylitis).
• Non-osteoarthritis arthritis.
• Planned total knee joint replacement.
• Gait disorders of neurological origin.
• Intra-articular hyaluronic acid injection in the study knee within 3 months prior to enrollment.
• Surgery or orthopedic intervention on the study knee in the last 3 months.
• Cancer
• Decompensated diabetes mellitus.
• Hematological diseases.
• Inability or unwillingness to comply with study procedures.
• Language barriers that prevent understanding of the informed consent form.
• Any other condition deemed by the investigator to preclude participation.
• Participation in another clinical study.

• Minimum Eligible Age: 21 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Pharmaxi Clinical Research LLC

UNKNOWN

Sponsor Role: collaborator

Yuria-Pharm

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Pharmaxi Clinical Research LLC

Kyiv, , Ukraine

Countries

Ukraine

Other Identifiers

DIART/REG-21

Identifier Type: REGISTRY

Identifier Source: secondary_id

DIART/REG-21

Identifier Type: -

Identifier Source: org_study_id