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Diabetic Foot UlcersPhase 3NCT00536744

Effectiveness of dermaPACE™ Device and Standard Treatment Compared to Standard Treatment Alone for Diabetic Foot Ulcers

A Phase 3 study testing acoustical pulse energy (extracorporeal shockwave) in people with Diabetic Foot Ulcers, run by SANUWAVE, Inc. at 23 sites in 3 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to compare the safety and effectiveness of the dermaPACE Device to sham application, when administered in conjunction with standard treatments used in the treatment of DFUs. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Diabetic Foot Ulcers
What is being tested?
acoustical pulse energy (extracorporeal shockwave)
Type of treatment
Medical device
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
206 participants
Where
23 sitesin 3 countries
Study dates
Oct 2007to Sep 2010
Phase
Phase 3
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Major Inclusion Criteria:

  • Male or female ≥ 18 years of age
  • Diabetes mellitus
  • One or more chronic foot ulcers (only one will be treated) that are located in the ankle area or below that has persisted a minimum of 30 days prior to the Screening visit
  • HbA1c ≤ 12%
  • Diabetic Foot Ulcers ≥ 1 cm2 and ≤ 16 cm2
  • Ulcer Grade I or II, Stage A according to the University of Texas Diabetic Wound Classification system
  • Ankle Brachial Index (ABI) ≥ 0.7 and ≤ 1.2, OR toe pressure > 50 mmHg, OR tcPO2> 40 mmHg.

Major Exclusion Criteria:

  • Subject is morbidly obese (Body Mass Index ≥ 40)
  • Subjects on dialysis
  • Diagnosis of foot ulcer involving osteomyelitis
  • Has evidence of prior ulcer in the same area
  • Multiple diabetic foot ulcers on the foot that either are connected by fistulas or are within 5 cm of the target ulcer
  • Subject's foot ulcer intended for study application has decreased in volume by 50% or more at the end of the two-week Run-in period as compared to the Screening visit.

Trial locations and contacts

23 sites in 3 countries.

23 sites in 3 countries

United States21 sites
  • Emory Orthopedic and Spine Center

    Atlanta, Georgia, 30329

  • Boston Medical Center

    Boston, Massachusetts, 02118

  • Beth Israel Deaconess Medical Center

    Boston, Massachusetts, 02215

  • Center for Clinical Research

    Castro Valley, California, 94115

  • Northwestern Univ. Div. of Plastic Surgery

    Chicago, Illinois, 60611

  • St. Vincent's Charity Hospital

    Cleveland, Ohio, 44115

  • Ohio State University

    Columbus, Ohio, 43221

  • Richard Galperin, DPM, PA

    Dallas, Texas, 75224

  • Veterans Administration Long Beach Healthcare

    Long Beach, California, 90822

  • Complete Family Foot Care

    McAllen, Texas, 78501

  • Aurora Health Care

    Milwaukee, Wisconsin, 53215

  • Nashville Family Footcare

    Nashville, Tennessee, 37203

  • North American Center for Limb Preservation

    New Haven, Connecticut, 06515

  • Fairfield County Foot Surgeons

    Norwalk, Connecticut, 06851

  • Phoenix VA Health Care System

    Phoenix, Arizona, 85012

  • HOPE Research Insititute

    Phoenix, Arizona, 85050

  • Mayo Clinic

    Rochester, Minnesota, 55905

  • Robert Wunderlich, DPM, PA

    San Antonio, Texas, 78212

  • Olive View - UCLA Medical Center

    Sylmar, California, 91342

  • Center for Palliative Wound Care; Calvary Hospital

    The Bronx, New York, 10461

  • Southern Arizona VA Healthcare System (SAVAHCS)

    Tucson, Arizona, 85723

Other trials in United States

Germany1 site
  • Mathias Spital

    Rheine, 48431

Other trials in Germany

United Kingdom1 site
  • Kings College Hospital

    London, SE59RS

Other trials in United Kingdom

About this study

Official title: Use of the dermaPACE™ (Pulsed Acoustic Cellular Expression) Device in Conjunction With Standard of Care in the Treatment of Diabetic Foot Ulcers

The purpose of this study is to compare the safety and effectiveness of the dermaPACE Device to sham application, when administered in conjunction with standard treatments used in the treatment of DFUs.

Read the detailed description

The objective of this clinical study is to compare the safety and effectiveness of the dermaPACE (Pulsed Acoustic Cellular Expression) Device to sham application, when administered in conjunction with the standard of care, in the treatment of DFUs.

Diabetic patients are susceptible to chronic foot ulcerations due to the effects of the diabetic's systemic disease halting the wound healing process. In the United States, 20.8 million people with active diabetes, and 41 million with pre-diabetic symptoms account for $132 billion dollars in healthcare costs per year. In 2002, 82,000 non-traumatic lower-limb amputations were performed on diabetics, corresponding to 60% of all lower limb amputations, usually preceded by a non-healing foot ulceration. Given the magnitude of this disease and the long-term effects and morbidity of amputation, DFUs require immediate and aggressive treatment to ascertain the best possible outcome for the diabetic patient.

Despite the development of advanced wound care products, there is still a need to find the most effective treatment for reducing the time required to close a DFU. At any given time, 3-4% of diabetics (600,000 patients) have a foot ulcer, and $2.5 billion was spent in 2002 in the United States treating DFUs. The average cost for a single episode of a foot ulcer has been reported to be $4,595.00 to $28,691.00. Shock wave devices, which utilize acoustic pressure waves, have been used for about 30 years in urology for lithotripsy. In the last decade this technology has gained FDA approval to treat chronic plantar fasciitis and lateral epicondylitis conditions that do not respond to conservative treatments (OssaTron® SANUWAVE, manufacturer). Further, clinical reports have indicated efficacy in treating many other orthopedic conditions including pseudoarthroses, calcification of the joints and avascular necrosis. This technology has also been shown to promote healing in several wound-healing applications, and it is worthwhile to continue to seek the full potential of this technology in wound healing.

Acoustic pressure waves initiate a biological response at the cellular level-stimulating production of angiogenic growth factors, including endothelial nitric oxide synthase (ENOS), vascular endothelial growth factor (VEGF), and proliferating cell nuclear antigen (PCNA). These factors are important components of the normal wound healing process. This cellular activation and growth factor expression stimulated by acoustic pressure wave treatment could play a decisive role in overcoming cell quiescence and increasing growth factor titers to levels sufficient to overcome proteases. This leads to the in-growing of newly formed vessels, and the increased cellular proliferation and tissue regeneration needed to heal a wound.

Clinical publications have recently reported the pressure wave induced mechanism described above can initiate and accelerate healing in burns, traumatic wounds and reconstructive skin flaps, and diabetic wounds. A pilot study using the dermaPACE device, performed in nine diabetic subjects with chronic leg ulcers has shown that this technology in patients with a history of chronic ulcers may achieve wound closure. Treatment with dermaPACE has the added benefits of being non-invasive and devoid of significant clinical side effects. Therefore, the objective of this study is to examine the safety and effectiveness of the dermaPACE acoustic pressure wave treatment device in combination with standard of care for the treatment of foot ulcers in diabetic patients.

The dermaPACE should offer an improved non-invasive standard of care that may shorten an otherwise lengthy healing process and therefore make later operative measures unnecessary. Given that conservative therapy may not be effective, dermaPACE may become a preferable alternative that would carry minimal risk based on the expected clinical outcomes described in this protocol. dermaPACE may improve patient quality of life when conservative therapy is not effective as well as provide a cost savings for the health care system.

Being tested
acoustical pulse energy (extracorporeal shockwave), Sham
Medical subject headings
Diabetic Foot

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • acoustical pulse energy (extracorporeal shockwave)Device

    Also called dermaPACE

    Acoustical pulse energy (extracorporeal shockwave) + Standard of care wound dressing.

  • ShamOther

    Non-energized (inactive - Sham) application + standard of care

Study groups in NCT00536744
Study groupRoleWhat they receive
Active PACE application - 4 applicationsActive comparatorApplication of acoustical pulse energy (extracorporeal shockwaves) to target ulcer + standard of care
Receives: Device: acoustical pulse energy (extracorporeal shockwave)
Inactive, non-energy applicationSham comparatorNon-energized (inactive - Sham)) application + standard of care
Receives: Other: Sham

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. The Primary Variable for Effectiveness of the dermaPACE Device Will be Assessed by Comparing the Incidence of Complete Wound Closure of the dermaPACE and Control Groups 12 Weeks Post Initial Application.

    Measured: 12 weeks post initial application

Secondary outcomes (1)
  1. Time to Wound Closure, Wound Closure Area and Volume Between Active and Control 12 Weeks Post Initial Application, Subject Pain Assessment Between Active and Control 24 Weeks Post Initial Application

    Measured: 12 weeks post initial application and 24 weeks post initial application

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Sep 2007 (estimated)
  2. Study startOct 2007
  3. Primary completionJun 2010
  4. Study completionSep 2010

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Care provider, Investigator
Enrolment
206 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00536744
Sponsor's protocol ID
SAN07-DERM01
Status last verified
Mar 2014
First submitted
26 Sep 2007
Last updated
14 Apr 2014
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing acoustical pulse energy (extracorporeal shockwave) in people with Diabetic Foot Ulcers, run by SANUWAVE, Inc. at 23 sites in 3 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 14 Apr 2014. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 23 sites in United States, Germany, United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 14 Apr 2014). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

The Primary Variable for Effectiveness of the dermaPACE Device Will be Assessed by Comparing the Incidence of Complete Wound Closure of the dermaPACE and Control Groups 12 Weeks Post Initial Application. (time frame: 12 weeks post initial application). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Apr 2014.

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