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

Yuria-Pharm

Status

Completed

Conditions

Osteoarthritis of the Knee

Knee Osteoarthritis

Degenerative Joint Disease

Study type

Observational

Funder types

Industry

Other

Identifiers

NCT06927934

DIART/REG-21 (Registry Identifier)

Details and patient eligibility

About

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.

Full 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.

Enrollment

55 patients

Sex

All

Ages

21+ years old

Volunteers

No Healthy Volunteers

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.