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| Sponsor: | ArthroCare Corporation |
|---|---|
| Information provided by (Responsible Party): | ArthroCare Corporation |
| ClinicalTrials.gov Identifier: | NCT00189592 |
Purpose
The purpose of this study is to evaluate the effectiveness of Coblation-based fasciotomy for relieving pain associated with recurring plantar fasciosis and, secondarily, to determine whether there may be additional potential benefits stemming from its use.
| Condition | Intervention | Phase |
|---|---|---|
|
Plantar Fasciosis Plantar Fasciitis |
Device: ArthroCare TOPAZ™ MicroDebrider™ using Coblation Procedure: Surgical Fasciotomy |
Phase IV |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | Plantar Fasciosis Treatment Using Coblation® Prospective, Double-Blind, Randomized Controlled Study |
| Enrollment: | 45 |
| Study Start Date: | August 2005 |
| Study Completion Date: | June 2008 |
| Primary Completion Date: | June 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: A
Percutaneous Fasciotomy
|
Device: ArthroCare TOPAZ™ MicroDebrider™ using Coblation
Percutaneous treatment of plantar fascia using the Topaz device. No incision performed.
|
|
Active Comparator: 2
Standard Fasciotomy
|
Procedure: Surgical Fasciotomy
Standard surgical fasciotomy using an incision to treat the plantar fascia.
|
Severe recalcitrant heel pain, resulting from repetitive trauma to the plantar fascia, is a relatively commonly observed phenomenon. Although this condition is frequently referred to as 'heel spurs', plantar fasciitis (acute inflammatory stage) and plantar fasciosis (chronic degeneration) are currently accepted as the more accurate terms. Symptoms most often occur during the first few steps in the morning but may also be effected during intense activity or with prolonged standing. The source of pain symptoms, which are usually perceived as a gradual onset of burning, is located at the origin of the plantar fascia at the calcaneous (heel bone). Risk factors such as low or high arches or over-pronation of the foot, systemic disease, or obesity may exacerbate pain.
More than two million Americans receive treatment each year for plantar fasciitis and fasciosis. Conservative treatment options for plantar fasciosis include rest, stretching, strengthening, and massage, progressing to non-steroidal anti-inflammatories, steroid injections or iontophoresis with continued recalcitrance. Orthotics, heel cups, night splints and plantar strapping are other conservative options frequently recommended by treating physicians. Patient outcomes and response to conservative measures are usually positive, with non-responsive cases, approximately 10% of all presenting cases, receiving surgical care. Extracorporeal shockwave treatment has recently been advocated for the recalcitrant cases and has shown to be effective in 60-80 percent of the cases. Plantar fascia release, either partial or complete, is commonly the surgical procedure of choice for treating plantar fasciosis. However, this surgery has a risk of complications and is thought to alter the biomechanics of the foot, which may be linked to post-operative lateral column pain and long-term disability. Because of the potential postoperative sequelae with plantar fascia release, it is valuable to examine less invasive surgical techniques for treating recalcitrant plantar fasciosis.
The concept of using a plasma RF-based microsurgical approach as a viable modality for treating tendinosis, and now, recalcitrant plantar fasciosis, was originally drawn from the research work conducted in patients treated for congestive heart failure using laser or RF-based transmyocardial revascularization (TMR). The mechanism of action behind the clinical success observed with laser and RF-based TMR was theorized to be associated with the localized angiogenic healing response noted to occur following the procedure. Localized angiogenesis had not been observed previously using mechanical devices for TMR, which were also less successful clinically. To substantiate adopting a TMR-like approach for treating tendinosis, the capability of plasma RF-based microsurgery for initiating an angiogenic healing response was examined in vivo using histology and biochemical analysis. The sum of several studies provides good evidence to suggest that plasma RF-based microsurgery can promote an angiogenic healing response using an appropriate application.
Preliminary clinical experience following plasma RF-based micro-tenotomy has demonstrated excellent success in treating chronic, refractive tendinosis. The investigators reported that this technique was technically simple to perform and was much less invasive than conventional surgery. Patients had a rapid and uncomplicated recovery and reported minimal to no pain 7-10 days following the procedure; their pain relief persisted or improved through 24 months. Magnetic resonance imaging correlated well with clinical results. These promising clinical findings, as well as the evidence from the basic research studies, led us to consider evaluating this plasma RF-based approach for treating symptomatic, chronic, recalcitrant heel pain resembling plantar fasciosis. The purpose of this study is to evaluate the effectiveness of Coblation-based fasciotomy for relieving pain associated with recalcitrant plantar fasciosis and, secondarily, to determine whether there may be additional potential benefits stemming from its use, such as reduced incidence of postoperative complications and improved function, compared to conventional surgery.
Eligibility| Ages Eligible for Study: | 18 Years to 72 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Diagnosis of plantar fasciitis/fasciosis by all of the following:
Exclusion Criteria:
Contacts and Locations| United States, Illinois | |
| Weil Foot & Ankle Institute | |
| Des Plaines, Illinois, United States, 60016 | |
| Principal Investigator: | Lowell S. Weil, Sr., DPM | Weil Foot & Ankle Institute |
More Information
| Responsible Party: | ArthroCare Corporation |
| ClinicalTrials.gov Identifier: | NCT00189592 History of Changes |
| Other Study ID Numbers: | A0105WW |
| Study First Received: | September 12, 2005 |
| Last Updated: | October 10, 2011 |
| Health Authority: | United States: Institutional Review Board |
|
plantar fascia plantar fasciosis plantar fasciitis Coblation fasciotomy conventional surgical fasciotomy |
heel spur heel pain aponeurosis plasma based radiofrequency angiogenesis |
|
Fasciitis Fasciitis, Plantar Musculoskeletal Diseases Foot Diseases |