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Platelet Rich Plasma to Treat Plantar Fasciitis

Primary Purpose

Plantar Fasciitis

Status
Completed
Phase
Phase 4
Locations
Netherlands
Study Type
Interventional
Intervention
L-PRP Injection
Corticosteroid Injection
Sponsored by
Zimmer Biomet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Plantar Fasciitis focused on measuring plantar fasciitis, platelet rich plasma, GPS

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • No bias to sex
  • > 18 years
  • Chronic plantar fasciitis or proximal recalcitrant plantar heel pain (6-12 months duration)
  • Failed conservative treatment
  • Able to understand the informed consent
  • VAS pain in morning by first steps higher as 5 (0-10 scale)

Exclusion Criteria:

  • Received local steroid injections within 6 weeks, physical/occupational therapies within 4 weeks, or non-steroidal anti-inflammatory within 1 week prior to randomization
  • Inability to fulfil follow-up criteria
  • Significant cardiovascular, renal or hepatic disease
  • Pregnant
  • (Local) malignancy
  • History of amenia (hemoglobin < 5.0 )
  • Previous surgery for plantar fasciitis
  • Active bilateral plantar fasciitis
  • Diagnosis of vascular insufficiency or neuropathy related to heel pain
  • Hypothyroidism
  • Diabetics
  • No other painful or function limited disorders of the foot and ankle

Sites / Locations

  • Haga ziekenhuis
  • Albert Schweitzer Ziekenhuis
  • Diaconessehuis
  • Academisch Ziekenhuis Maastricht
  • St Elisabeth Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

L-PRP Injection

Steroid Injection

Arm Description

L-PRP produced with Biomet Recover L-PRP Platelet Separation Kit

Corticosteroid injections

Outcomes

Primary Outcome Measures

Percentage of successfully treated patients

Secondary Outcome Measures

Pain reduction
Function
Patient satisfaction
Complications and reinventions

Full Information

First Posted
September 22, 2008
Last Updated
March 13, 2017
Sponsor
Zimmer Biomet
Collaborators
Elisabeth-TweeSteden Ziekenhuis, Diaconessenhuis Leiden Netherlands, Biomet Nederland BV
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1. Study Identification

Unique Protocol Identification Number
NCT00758641
Brief Title
Platelet Rich Plasma to Treat Plantar Fasciitis
Official Title
Use of PRP to Treat Plantar Fasciitis, Blinded and Randomized as a Multi Center Study
Study Type
Interventional

2. Study Status

Record Verification Date
June 2016
Overall Recruitment Status
Completed
Study Start Date
September 2009 (undefined)
Primary Completion Date
January 2016 (Actual)
Study Completion Date
January 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Zimmer Biomet
Collaborators
Elisabeth-TweeSteden Ziekenhuis, Diaconessenhuis Leiden Netherlands, Biomet Nederland BV

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Rationale: The standard treatment of chronic plantar fasciitis is corticosteroid injections. Corticosteroid injection give temporarily pain reduction, but no healing. Blood platelets initiate the natural healing rate. GPS ® gives an eightfold concentrate platelets of patients own blood. Injection of these platelets in the tendon might induce a healing rate. Objective: To compare the efficacy of autologous platelet concentrate injections with corticosteroid injection in patients suffering from plantar fasciitis with respect to pain and function.
Detailed Description
Plantar fasciitis is the most common cause of foot complaints in the United States, making up 11 to 15 percent of the foot symptoms requiring professional care among adults (Pfeffer et al., 1999; Cole et al., 2005). A 2004 publication found that there are approximately 1 million patient visits per year to office-based physicians and hospital outpatient departments in the United States for plantar fasciitis (Riddle et al., 2004). This figure does not consider podiatric physicians visits, including these numbers would raise the overall physician visits related to plantar fasciitis considerably. The incidence of plantar fasciitis peaks in people between the ages of 40 to 60 years with no bias towards either sex (Taunton et al., 2002) The underlying condition that causes plantar fasciitis is a degenerative tissue condition that occurs near the site of origin of the plantar fascia at the medial tuberosity of the calcaneous (Buchbinder, 2004). In acute cases, plantar fasciitis is characterized by classical signs of inflammation including pain, swelling and loss of function. For more chronic conditions, however, inflammation is not the underlying tissue disruption. In fact, histology of chronic cases has shown no signs of inflammatory cell invasion into the affected area (Lemont et al., 2003). The tissue instead is characterized histological by infiltration with macrophages, lymphocytes, and plasma cells; tissue destruction; and repair involving immature vascularization and fibrosis (Lemont et al., 2003). The normal fascia tissue is replaced by an angiofibroblastic hyperplastic tissue which insuitates itself throughout the surrounding tissue creating a self-perpetuating cycle of degeneration (Lemont et al., 2003). In these chronic cases, the suffix 'itis' is a misnomer with plantar fasciosis being a more apt description of the underlying histology. Conservative treatments including stretching protocols and foot orthoses resolve many cases of plantar fasciitis, with reports for patients in orthopedic practices being around 80 percent resolution (Cole et al., 2005; Wolgin et al., 1994; Martin et al., 1998; Davies et al., 1999). For more chronic cases, a number of non-surgical interventions are utilized including extracorperal shock wave therapy and corticosteroid injections (Cole et al., 2005; Speed et al., 2003; Acevedo, Beskin, 1998). The use of corticosteroids is particularly troubling as several studies have linked plantar fascial rupture to repeated local injections of a corticosteroid (Cole et al., 2005; Sellman, 1994; Leach et al., 1978; Acevedo, Beskin, 1998). All of these methods are limited in their efficacy for cases of chronic plantar fasciitis due to the fact that none of them adequately addresses the full scope of the underlying tissue degeneration. This frequently leaves surgical intervention as the only viable option in these chronic cases. The goal of treatment for chronic plantar fasciitis should be to cease and ultimately reverse the degenerating tissue disruption that is at the root of the condition. The three steps critical to full repair of the effected tissue are: Enhancing the influx and proliferation of fibroblasts into the effected area. This will allow for a tissue bed that is extremely receptive to vascularization Promote angiogenesis to develop a mature vascular structure in the effected area With a mature vascularization, collagen deposition can then occur, resulting in the organization of fully mature tendon tissue The injection of platelet-rich-plasma (PRP) into the effected tissue addresses all three healing stages necessary to reverse the degenerative process. The individual cytokines present in the platelet α-granules have been shown to enhance fibroblast migration and proliferation, upregulate vascularization, and increases collagen deposition in a variety of in vitro and in vivo settings [Molloy 2004]. Autologous PRP contains concentrated white blood cells and platelets that are suspended in plasma. Since an acidic anticoagulant (Anticoagulant Citrate Dextrose Solution A) is used to allow for processing of the whole blood via centrifugation, the PRP must be buffered to increase the pH to normal physiologic levels prior for injection into the effected tissue. This is accomplished with the addition of an 8.4% sodium bicarbonate solution at a ratio 0.05cc of sodium bicarbonate solution to 1cc of platelet concentrate. The resulting buffered platelet concentrate contains approximately 6 to 8 times concentration of platelets compared to baseline whole blood. The cytokines present in platelet α-granules have been shown to affect the three healing stages necessary to reverse a chronic plantar fasciitis condition (Molloy et al., 2003). Additionally, many of these cytokines have been seen to work in a dose dependent manner (Molloy et al., 2003). A PRP injection into the effected area of tissue would provide concentrated levels of cytokines that should result in a healing cascade that halts and ultimately reverses the underlying pathology of elbow tendinosis. This treatment concept directly addresses the existing condition and should prove to be a superior alternative to current conservative treatments for chronic plantar fasciitis. The objective of this clinical investigation is to compare the efficacy of autologous platelet concentrate injections with corticosteroid injection in patients suffering from plantar fasciitis with respect to pain and function. Primary question Does injection with autologous platelet concentrate results in a larger percentage of successfully treated patients after 6 month as injection corticosteroid injection? Secondary questions Does injection with autologous platelet concentrate has a larger pain reduction as injection of corticosteroid injection? (VAS) Does injection with autologous platelet concentrate has a larger improvement in function as corticosteroid injection? (AOFAS, WHOQol) Does injection with autologous platelet concentrate has a larger amount of satisfied patients as of corticosteroid injection? (WHOQol, satisfaction)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Plantar Fasciitis
Keywords
plantar fasciitis, platelet rich plasma, GPS

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
115 (Actual)

8. Arms, Groups, and Interventions

Arm Title
L-PRP Injection
Arm Type
Experimental
Arm Description
L-PRP produced with Biomet Recover L-PRP Platelet Separation Kit
Arm Title
Steroid Injection
Arm Type
Active Comparator
Arm Description
Corticosteroid injections
Intervention Type
Device
Intervention Name(s)
L-PRP Injection
Intervention Description
L-PRP produced with Biomet Recover L-PRP Platelet Separation Kit
Intervention Type
Drug
Intervention Name(s)
Corticosteroid Injection
Other Intervention Name(s)
Corticosteroid
Intervention Description
kenacort 40 mg/ml triamcinolon acetonide
Primary Outcome Measure Information:
Title
Percentage of successfully treated patients
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Pain reduction
Time Frame
0-12 months
Title
Function
Time Frame
0-12 months
Title
Patient satisfaction
Time Frame
0-12 months
Title
Complications and reinventions
Time Frame
0-12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: No bias to sex > 18 years Chronic plantar fasciitis or proximal recalcitrant plantar heel pain (6-12 months duration) Failed conservative treatment Able to understand the informed consent VAS pain in morning by first steps higher as 5 (0-10 scale) Exclusion Criteria: Received local steroid injections within 6 weeks, physical/occupational therapies within 4 weeks, or non-steroidal anti-inflammatory within 1 week prior to randomization Inability to fulfil follow-up criteria Significant cardiovascular, renal or hepatic disease Pregnant (Local) malignancy History of amenia (hemoglobin < 5.0 ) Previous surgery for plantar fasciitis Active bilateral plantar fasciitis Diagnosis of vascular insufficiency or neuropathy related to heel pain Hypothyroidism Diabetics No other painful or function limited disorders of the foot and ankle
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
T Gosens, MD, PhD
Organizational Affiliation
St Elisabeth Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
H.M. Schuller, PhD, MD
Organizational Affiliation
Diaconessehuis Leiden
Official's Role
Principal Investigator
Facility Information:
Facility Name
Haga ziekenhuis
City
DenHaag
Country
Netherlands
Facility Name
Albert Schweitzer Ziekenhuis
City
Dordrecht
ZIP/Postal Code
3318
Country
Netherlands
Facility Name
Diaconessehuis
City
Leiden
Country
Netherlands
Facility Name
Academisch Ziekenhuis Maastricht
City
Maastricht
ZIP/Postal Code
6229
Country
Netherlands
Facility Name
St Elisabeth Hospital
City
Tilburg
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
31603721
Citation
Peerbooms JC, Lodder P, den Oudsten BL, Doorgeest K, Schuller HM, Gosens T. Positive Effect of Platelet-Rich Plasma on Pain in Plantar Fasciitis: A Double-Blind Multicenter Randomized Controlled Trial. Am J Sports Med. 2019 Nov;47(13):3238-3246. doi: 10.1177/0363546519877181. Epub 2019 Oct 11.
Results Reference
derived
PubMed Identifier
20398269
Citation
Peerbooms JC, van Laar W, Faber F, Schuller HM, van der Hoeven H, Gosens T. Use of platelet rich plasma to treat plantar fasciitis: design of a multi centre randomized controlled trial. BMC Musculoskelet Disord. 2010 Apr 14;11:69. doi: 10.1186/1471-2474-11-69.
Results Reference
derived

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Platelet Rich Plasma to Treat Plantar Fasciitis

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