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Comparison of Hyaluronic Acid and Platelet-rich Plasma Injections

B

Bezmialem Vakif University

Status

Completed

Conditions

Knee Osteoarthritis

Treatments

Biological: Hyaluronic acid injection
Biological: Platelet-rich plasma injection

Study type

Interventional

Funder types

Other

Identifiers

NCT03761472
71306642-050.01.04-

Details and patient eligibility

About

This study aims to compare the effects of hyaluronic acid injection and platelet rich plasma injection in terms of pain, physical function and femoral cartilage thickness in short term treatment in patients with knee osteoarthritis.

Full description

Platelet-rich plasma and hyaluronic acid injections are both popular treatments and commonly used for treatment of knee osteoarthritis. Even though there are many studies investigating the effectiveness of these treatments, the results are mostly qualitative. Also there are a few studies comparing these two treatment modalities. In this study the investigators aim to compare these modalities both for self-reported data (pain, physical function) and objective measurement data (femoral cartilage thickness via ultrasonography). Patients with unilateral osteoarthritis/unilateral complaint will be included in the study. Unaffected side will be controls for each group.

Enrollment

40 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subject is able to consent
  • Subject meets Osteoarthritis Research Society International (OARSI) criteria for knee osteoarthritis
  • Subject has radiographic Kellgren-Lawrence grade 2-3 osteoarthritis
  • Unilateral osteoarthritis/complaint

Exclusion criteria

  • Past or actual knee infection
  • History of surgery, fracture on knee
  • Collagen tissue disease
  • Systemic inflammatory disease (rheumatoid arthritis, spondyloarthritis etc.)
  • Systemic diseases (diabetes, hematologic diseases, endocrinopathies, renal failure, liver failure)
  • Knee injection in past 6 months
  • Immunodeficiency
  • Pregnant/breastfeeding
  • Malignancy

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 4 patient groups

Hyaluronic acid injection
Active Comparator group
Description:
Hyaluronic acid 48 mg 2.0% in 2 ml solution, once initially.
Treatment:
Biological: Hyaluronic acid injection
Platelet-rich plasma injection
Active Comparator group
Description:
Platelet-rich plasma 5 ml, once initially
Treatment:
Biological: Platelet-rich plasma injection
Unaffected side Hyaluronic acid
No Intervention group
Description:
Unaffected sides of the patients will be controls for hyaluronic acid group, no intervention.
Unaffected side Platelet-rich plasma
No Intervention group
Description:
Unaffected sides of the patients will be controls for Platelet-rich plasma group, no intervention.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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