Study on the Use of a Concentrated Growth Factor Preparation Kit for the Treatment of Knee Osteoarthritis

NCT06869200 | Completed Results

• 1 other identifier: HZJKCGFOA202501
• Study Type: interventional
• Target: 104
• Locations: 1 country
• Sites: 3

Brief Summary

The goal of this clinical trial is to evaluate the effectiveness and safety of an autologous platelet-rich concentrated growth factor (CGF) preparation kit for the treatment of knee osteoarthritis in patients diagnosed with this condition. The main question it aims to answer is: Can the CGF preparation kit effectively improve symptoms and reduce pain in patients with knee osteoarthritis compared to a control intervention? Researchers will compare the CGF treatment group to a control group using platelet-rich plasma (PRP) to see if the CGF intervention results in greater improvements in knee function and pain relief. Participants will: Undergo three intra-articular injections of CGF or PRP into the knee joint at weekly intervals. Complete assessments including the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) and Visual Analog Scale (VAS) for pain at specified intervals. Be monitored for safety and potential adverse events throughout the study period. Study design: Prospective, multicenter, single-blind, randomized controlled, non-inferiority clinical trial. Sample size: 104 cases, with 52 cases in the experimental group and 52 cases in the control group.

Conditions

Knee Osteoarthritis

Keywords

knee osteoarthritis; concentrated growth factors (CGF); platelet-rich plasma; Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC); Intra-articular Injection

Study Arms (2)

CGF Treatment Group

EXPERIMENTAL

Participants in this arm will receive three intra-articular injections of Concentrated Growth Factor (CGF) prepared using the autologous platelet-rich CGF preparation kit. The injections will be administered at weekly intervals over a period of three weeks.

Device: Concentrated Growth Factor (CGF) Intra-articular Injection

PRP Treatment Group

ACTIVE COMPARATOR

Participants in this arm will receive three intra-articular injections of Platelet-Rich Plasma (PRP) prepared using a disposable PRP preparation device. The injections will be administered at weekly intervals over a period of three weeks.

Device: Platelet-Rich Plasma (PRP) Intra-articular Injection

Interventions

Platelet-Rich Plasma (PRP) Intra-articular Injection DEVICE

Preparation Method: The PRP is prepared using a disposable PRP preparation device that separates and concentrates platelets from the patient's blood. This process enriches the plasma with platelets and associated growth factors. Rationale: PRP has been widely used in clinical practice for its ability to promote tissue healing and reduce inflammation in osteoarthritis. It serves as an active comparator in this study, allowing for a direct comparison of the therapeutic efficacy and safety profile of CGF against a well-established treatment modality.

PRP Treatment Group

Concentrated Growth Factor (CGF) Intra-articular Injection DEVICE

Preparation Method: The CGF is prepared using an autologous platelet-rich preparation kit specifically designed to concentrate growth factors from the patient's own blood. The process involves a specialized centrifugation technique that yields a high concentration of growth factors, including platelet-derived growth factor (PDGF), transforming growth factor-beta (TGF-β), and other bioactive molecules. Rationale: This intervention leverages the body's natural healing response by utilizing autologous growth factors to enhance the repair of cartilage and other joint tissues affected by osteoarthritis. The high concentration of bioactive molecules in CGF is believed to provide a more potent therapeutic effect compared to other platelet-rich therapies.

CGF Treatment Group

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Age ≥ 18 years, with no gender restrictions;
• Patients diagnosed with knee osteoarthritis according to the "Chinese Guidelines for the Diagnosis and Treatment of Osteoarthritis (2024 Edition)" by the Chinese Osteoarthritis Diagnosis and Treatment Guidelines Expert Group;
• Radiographic evidence of knee osteoarthritis with Kellgren-Lawrence grading of II to IV;
• Visual Analog Scale (VAS) pain score ≥ 4 (moderate or higher pain) and WOMAC score ≥ 24;
• For participants with eligible bilateral knee osteoarthritis, the more severely affected knee will be treated, while the other knee will not be intervened during the study period. If the severity is equal on both sides, the left knee will be selected for intervention;
• The patient or their legal guardian is able to understand the purpose of the study and provide informed consent.

You may not qualify if:

• Patients with a confirmed diagnosis of other inflammatory diseases of the knee joint, such as rheumatoid arthritis, psoriatic arthritis, or gouty arthritis; Patients with a confirmed diagnosis of bleeding disorders (e.g., allergic purpura, hemophilia, idiopathic thrombocytopenic purpura), hematologic malignancies (e.g., leukemia), or those with unconfirmed bleeding disorders but coagulation dysfunction (coagulation parameters PT, APTT, INR \> 1.5 times the upper limit of normal);
• Patients who have undergone or are planned to undergo knee osteoarthritis surgery within the past 6 months or during the trial period;
• Patients with local infections at the injection site (e.g., septic arthritis, tuberculous arthritis, or local soft tissue infections) or severe systemic infections (e.g., sepsis);
• Patients with untreated malignant diseases such as malignancies, which may interfere with the safety and efficacy assessments of the study and affect the patient's participation in the study;
• Patients with severe hepatic or renal dysfunction \[hepatic function indicators alanine aminotransferase (ALT), aspartate aminotransferase (AST) \> 2 times the upper limit of normal; renal function indicators serum creatinine (Cr), blood urea nitrogen (BUN) \> 2 times the upper limit of normal\];
• Patients with hemoglobin \< 10 g/dL or platelet count \< 125 × 10\^9/L;
• Patients who have used any Chinese or Western medications or therapies for the treatment of knee osteoarthritis within 1 week prior to randomization;
• Patients who have received intra-articular injections or related drug therapies within the past 3 months;
• Women who are planning a pregnancy, breastfeeding, or pregnant during the entire clinical study period;
• Patients who have participated in other interventional drug or medical device clinical trials within 1 month prior to enrollment;
• Other situations where the investigator deems the patient unsuitable for participation in this study.

Sponsors & Collaborators

• Nanfang Hospital, Southern Medical University: collaborator
• Shantou Central Hospital: collaborator
• Third Affiliated Hospital, Sun Yat-Sen University: collaborator
• Guangdong Hongzhi Health Technology: lead

Study Sites (3)

Nanfang Hospital,

Guangzhou, Guangdong, 510515, China

Location

Shantou Central Hospital

Shantou, Guangdong, 515000, China

Location

The Third Affiliated Hospital,Sun Yat-Sen University.

Guangdong, Guangzhou, 510000, China

Location

MeSH Terms

Conditions

Osteoarthritis, Knee

Interventions

Injections, Intra-Articular

Condition Hierarchy (Ancestors)

Osteoarthritis; Arthritis; Joint Diseases; Musculoskeletal Diseases; Rheumatic Diseases

Intervention Hierarchy (Ancestors)

Injections; Drug Administration Routes; Drug Therapy; Therapeutics

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: PARTICIPANT
• Masking Details: As the primary outcome measure of this study relies on subjective evaluation by the participants, a single-blind design is adopted to avoid bias introduced by participants' evaluations. During the informed consent process, investigators should clearly inform participants that they will be randomly assigned to one of the two treatment groups, but they will not be informed of which group they have been allocated to until the end of the study.
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: March 5, 2025
• First Posted: March 11, 2025
• Study Start: March 13, 2025
• Primary Completion: July 3, 2025
• Study Completion: September 17, 2025
• Last Updated: July 7, 2026
• Results First Posted: July 7, 2026

Record last verified: 2026-07

Data Sharing

• IPD Sharing: Will not share

Locations

CN (3)