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Comparison of Autologous Platelet-rich Plasma With Hyaluronic Acid for the Treatment of Osteoarthritis of the Knee Joint

Primary Purpose

Osteoarthritis, Knee

Status
Completed
Phase
Phase 3
Locations
Korea, Republic of
Study Type
Interventional
Intervention
PRP
Hyaluronic acid
Sponsored by
Samsung Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis, Knee focused on measuring Osteoarthritis, platelet-rich plasma, hyaluronic acid

Eligibility Criteria

40 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with osteoarthritis of knee (by American College of Rheumatology Criteria) and Kellgren-Lawrence grade I ~ III
  • More than 40 out of 100-mm VAS scale for pain at screening and baseline
  • Participant is willing and able to give informed consent for participation in the study

Exclusion Criteria:

  • Patients with Hb values < 10 g/dl and platelet values < 100,000/ul
  • Patients with a current or medical history of autoimmune disease
  • Recent fever ( within 2 weeks) or serious illness
  • Local infection at the site of the procedure
  • Corticosteroid injection at treatment site within 1 month
  • Systematic use of corticosteroids within 2 weeks
  • Female participants who are pregnant, lactating or planning pregnancy during the course of the study
  • Patients who have been administered with immunosuppressants within the past 6 weeks
  • Patients who are enrolled in any other clinical trials within 4 weeks
  • Patients who the principal investigator considers inappropriate for participation in the clinical trial for reasons other than those listed above

Sites / Locations

  • Samsung Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

PRP group

Hyaloronan group

Arm Description

Patients randomized to this group of treatment will receive 1 blinded knee intra-articular injections of autologous Platelet-Rich Plasma (3ml).

Patients randomized to this group of treatment will receive 1 blinded knee intra-articular injections of hyaluronic acid (3ml)

Outcomes

Primary Outcome Measures

Change from baseline in International Knee Documentation Committee subjective score at week 24
International Knee Documentation Committee subjective score for both groups

Secondary Outcome Measures

Change from baseline in VAS (Visual Analogue scale) for pain during walking
VAS (Visual Analogue scale) for pain during walking for both groups of treatment
Change from baseline in Western Ontario and McMaster Universities Arthritis Index
Western Ontario and McMaster Universities Arthritis Index variation for both groups Subscale analysis of pain, stiffness, function also contain
Number of Participants with Adverse Events
All adverse events included
Change from baseline in Samsung Medical Center Patellofemoral score (SMC patellofemoral score)
Samsung Medical Center Patellofemoral score for both groups of treatment
Patient global assessment
Patient global assessment was evaluated for improvement of symptoms using 100mm VAS.
Change from baseline in International Knee Documentation Committee subjective score at week 6, week 12
International Knee Documentation Committee subjective score for both groups

Full Information

First Posted
July 18, 2014
Last Updated
December 9, 2015
Sponsor
Samsung Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT02211521
Brief Title
Comparison of Autologous Platelet-rich Plasma With Hyaluronic Acid for the Treatment of Osteoarthritis of the Knee Joint
Official Title
Randomized, Double Blind, Comparison Clinical Trial to Test the Efficacy and Safety of Intraarticular Injection of Autologous Platelet-rich Plasma (PRP) for the Treatment of Osteoarthritis of the Knee Joint
Study Type
Interventional

2. Study Status

Record Verification Date
December 2015
Overall Recruitment Status
Completed
Study Start Date
August 2014 (undefined)
Primary Completion Date
October 2015 (Actual)
Study Completion Date
October 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Samsung Medical Center

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to compare the efficacy of platelet-rich plasma versus hyaluronic acid intra-articular injections for the treatment of osteoarthritis of knee joint. The hypothesis is that PRP intra-articular injection is comparable or even better than hyaluronic acid injection.
Detailed Description
Osteoarthritis (OA) has a significant impact on our society. The limited regenerative capacity of cartilage is part of this problem. Existing degenerative lesions lead to accelerated deterioration of the articular (joint) surface leading to end-stage arthritis. In particular, the most recent knowledge regarding tissue biology highlights a complex regulation of growth factors (GFs) for the normal tissue structure and the reaction to tissue damage. The influence of GFs on cartilage repair is now widely investigated in vitro and in vivo. Platelet Rich Plasma (PRP) is a simple, low- cost and minimally- invasive method that allows one to obtain a natural concentrate of autologous GFs from the blood, and it is increasingly applied in the clinical practice to treat knee degenerative pathology, such as chondropathy and early OA. The biological rational of PRP is that platelets contain storage pools of GFs, cytokines, chemokines and many other mediators.Although its widespread application, there are little high level studies in the literature to demonstrate the real efficacy of PRP. The investigators hypothesized that intra-articular injections of PRP to treat knee osteoarthritis could determine pain relief and recovery of knee function with overall clinical outcome comparable or even better than viscosupplementation, which is a common injective approach applied in this kind of pathology. To this purpose the investigators designed a double blind randomized controlled trial comparing PRP vs viscosupplementation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Knee
Keywords
Osteoarthritis, platelet-rich plasma, hyaluronic acid

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
110 (Actual)

8. Arms, Groups, and Interventions

Arm Title
PRP group
Arm Type
Experimental
Arm Description
Patients randomized to this group of treatment will receive 1 blinded knee intra-articular injections of autologous Platelet-Rich Plasma (3ml).
Arm Title
Hyaloronan group
Arm Type
Active Comparator
Arm Description
Patients randomized to this group of treatment will receive 1 blinded knee intra-articular injections of hyaluronic acid (3ml)
Intervention Type
Biological
Intervention Name(s)
PRP
Other Intervention Name(s)
GPS III, Biomet Biologics, Warsaw, Ind, USA
Intervention Description
3ml of PRP
Intervention Type
Drug
Intervention Name(s)
Hyaluronic acid
Other Intervention Name(s)
LBSA0103, 60 mg/3ml, LG Life Sciences, Korea
Intervention Description
3ml hyaluronic acid
Primary Outcome Measure Information:
Title
Change from baseline in International Knee Documentation Committee subjective score at week 24
Description
International Knee Documentation Committee subjective score for both groups
Time Frame
Baseline, Week 24
Secondary Outcome Measure Information:
Title
Change from baseline in VAS (Visual Analogue scale) for pain during walking
Description
VAS (Visual Analogue scale) for pain during walking for both groups of treatment
Time Frame
Baseline, Week 6, Week 12, Week 24
Title
Change from baseline in Western Ontario and McMaster Universities Arthritis Index
Description
Western Ontario and McMaster Universities Arthritis Index variation for both groups Subscale analysis of pain, stiffness, function also contain
Time Frame
Baseline, Week 6, Week 12, Week 24
Title
Number of Participants with Adverse Events
Description
All adverse events included
Time Frame
Week 6, Week 12, Week 24
Title
Change from baseline in Samsung Medical Center Patellofemoral score (SMC patellofemoral score)
Description
Samsung Medical Center Patellofemoral score for both groups of treatment
Time Frame
Baseline, Week 6, Week 12, Week 24
Title
Patient global assessment
Description
Patient global assessment was evaluated for improvement of symptoms using 100mm VAS.
Time Frame
Week 6, Week 12, Week 24
Title
Change from baseline in International Knee Documentation Committee subjective score at week 6, week 12
Description
International Knee Documentation Committee subjective score for both groups
Time Frame
Baseline, Week 6, Week 12
Other Pre-specified Outcome Measures:
Title
Level of white blood cell count of platelet rich plasma
Description
Assessment of level of WBC, platelet and several growth factors of platelet rich plasma Assessment of level of white blood cell count of platelet rich plasma
Time Frame
baseline
Title
Level of platelet of platelet rich plasma
Description
Assessment of level of platelet of platelet rich plasma
Time Frame
baseline
Title
Level of growth factors of platelet rich plasma
Description
Assessment of level several growth factors of platelet rich plasma (platelet derived growth factor, transforming growth factor -b1, vascular endothelial growth factor, epidermal growth factor, fibroblast growth factor etc)
Time Frame
baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with osteoarthritis of knee (by American College of Rheumatology Criteria) and Kellgren-Lawrence grade I ~ III More than 40 out of 100-mm VAS scale for pain at screening and baseline Participant is willing and able to give informed consent for participation in the study Exclusion Criteria: Patients with Hb values < 10 g/dl and platelet values < 100,000/ul Patients with a current or medical history of autoimmune disease Recent fever ( within 2 weeks) or serious illness Local infection at the site of the procedure Corticosteroid injection at treatment site within 1 month Systematic use of corticosteroids within 2 weeks Female participants who are pregnant, lactating or planning pregnancy during the course of the study Patients who have been administered with immunosuppressants within the past 6 weeks Patients who are enrolled in any other clinical trials within 4 weeks Patients who the principal investigator considers inappropriate for participation in the clinical trial for reasons other than those listed above
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chul-WOn Ha, MD, PhD
Organizational Affiliation
Samsung Medical Center, Sungkyunkwan University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Samsung Medical Center
City
Seoul
ZIP/Postal Code
135-710
Country
Korea, Republic of

12. IPD Sharing Statement

Citations:
PubMed Identifier
23104611
Citation
Cerza F, Carni S, Carcangiu A, Di Vavo I, Schiavilla V, Pecora A, De Biasi G, Ciuffreda M. Comparison between hyaluronic acid and platelet-rich plasma, intra-articular infiltration in the treatment of gonarthrosis. Am J Sports Med. 2012 Dec;40(12):2822-7. doi: 10.1177/0363546512461902. Epub 2012 Oct 25.
Results Reference
background
PubMed Identifier
22513879
Citation
Spakova T, Rosocha J, Lacko M, Harvanova D, Gharaibeh A. Treatment of knee joint osteoarthritis with autologous platelet-rich plasma in comparison with hyaluronic acid. Am J Phys Med Rehabil. 2012 May;91(5):411-7. doi: 10.1097/PHM.0b013e3182aab72.
Results Reference
background
PubMed Identifier
21831567
Citation
Kon E, Mandelbaum B, Buda R, Filardo G, Delcogliano M, Timoncini A, Fornasari PM, Giannini S, Marcacci M. Platelet-rich plasma intra-articular injection versus hyaluronic acid viscosupplementation as treatments for cartilage pathology: from early degeneration to osteoarthritis. Arthroscopy. 2011 Nov;27(11):1490-501. doi: 10.1016/j.arthro.2011.05.011. Epub 2011 Aug 10.
Results Reference
background
PubMed Identifier
24192391
Citation
Sundman EA, Cole BJ, Karas V, Della Valle C, Tetreault MW, Mohammed HO, Fortier LA. The anti-inflammatory and matrix restorative mechanisms of platelet-rich plasma in osteoarthritis. Am J Sports Med. 2014 Jan;42(1):35-41. doi: 10.1177/0363546513507766. Epub 2013 Nov 5.
Results Reference
background
PubMed Identifier
33523756
Citation
Park YB, Kim JH, Ha CW, Lee DH. Clinical Efficacy of Platelet-Rich Plasma Injection and Its Association With Growth Factors in the Treatment of Mild to Moderate Knee Osteoarthritis: A Randomized Double-Blind Controlled Clinical Trial As Compared With Hyaluronic Acid. Am J Sports Med. 2021 Feb;49(2):487-496. doi: 10.1177/0363546520986867.
Results Reference
derived

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Comparison of Autologous Platelet-rich Plasma With Hyaluronic Acid for the Treatment of Osteoarthritis of the Knee Joint

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