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NCT Number: NCT02783066

Novel Offloading for Diabetic Foot Ulcers With PulseFlow: A Prospective Study

Diabetic foot ulceration (DFU) is a common and largely preventable complication of diabetes. While most of these ulcers can be treated successfully, some will persist and become infected. Ultimately, nearly one fifth of patients with infected lower-extremity diabetic ulcers will require amputation of the affected limb, resulting in staggering costs for both the patient and the healthcare system. Prevention by identifying people at higher risk is key for better clinical management of such patients. It is not uncommon for patients suffering from diabetes to have concomitant lower extremity edema or venous insufficiency and they subsequently may benefit from graduated compression. However, because of the common association of peripheral arterial disease (PAD) in patients with diabetes, most clinicians are reluctant to apply compressive dressings in fear of exacerbating the symptoms of PAD and possibility of gangrene.

A novel low voltage, battery powered medical device, PulseFlow DF® (The Diabetic Boot Company, Ltd. UK) has endeavored to assist in the treatment of Diabetic Foot Ulcers. The device provides hybrid functionality i.e. mobile air bladder pump at plantar arch and offloading boot. The air bladder inflates to 160 mmHg for approx. 1 second then deflates back to atmospheric pressure, allowing the plantar vessels sufficient time to refill. The offloading boot design holds the foot and lower leg in a position that reduces shear and friction forces and provides a reduction in plantar pressure.

The PulseFlow DF is designed to record how many hours of blood pumping it has delivered. This data will be downloaded at each clinic visit. The boot cannot pump blood around the participant's foot unless fitted correctly and the battery is charged up overnight.

The purpose of this study is to conduct an interventional study study with N=15 diabetic subjects with active foot ulcers to assess whether PulseFlow foot compression device can help improve lower extremity perfusion, whilst improving balance and spatio-temporal parameters of gait.

The key goals of the proposed project are to test whether a specially designed compression device can improve lower extremity perfusion, whilst also simultaneously improving the balance and walking performance. Investigators envision the use of this specially designed offloading device with compression capability will help reduce the incidence of diabetic foot ulcers in high-risk diabetic patients. In addition, investigators assumed the proposed device might enhance daily physical activity as well as walking performance. Investigators will conduct a prospective clinical study to validate these hypotheses. Potential changes in walking and spontaneous daily physical activities will be assessed using validated technologies that include walking analyzer system, balance assessment using body worn sensors, and computerized pressure insoles.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Baylor College of Medicine

Houston, Texas, 77030, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18- 80 years old
  • type II diabetes with active plantar ulcer,

Exclusion criteria

  • Non-ambulatory or unable to stand without help or walk a distance of at least 6 feet without assistance
  • Plantar ulcer on arch of the foot
  • Patients with PAD (Ankle Brachial Index < 0.5)
  • Acute foot fracture
  • Heart failure
  • Pregnant women
  • Patients on immunosuppressive drugs
  • Participation in an interventional study in the last 30 days
  • Major amputation
  • Patients unable or unwilling to participate in all procedures and follow-up evaluations.

Treatment and study plan

Offloading boot: PulseFlow

Device

A new offloading boot, which may enhance balance, gait, and lower extremity blood flow

Primary outcomes

  1. Lower Extremity Perfusion Change From Baseline to 4 Weeks

    Time frame: baseline and 4 weeks

    Skin perfusion measured in the ankle using Sensilase device. To measure Skin Perfusion Pressure (SPP), a pressure cuff is first automatically inflated to occlude arterial bed blood flow; this is verified by PAD-IQ by determining when perfusion has stopped. The pressure is then automatically released at a controlled rate while the cuff pressure and skin perfusion are measured. A graph displays pressure and perfusion during cuff deflation and indicates the pressure at which skin perfusion is found to return.

  2. Gait Speed Difference Between Pulseflow Offflaoding and Standard Offloading

    Time frame: baseline

    the quality of walking while wearing Pulseflow offflaoding compared to standard offloading

Secondary outcomes

  1. Adherence

    Time frame: 4 weeks

    adherence to wear offloading boot by downloading from the study device to a specific developed software. The measure is the mean number of minutes the offloading boot was worn for over the course of 4 weeks

  2. Wound Size Change From Baseline to 4 Weeks.

    Time frame: baselineand and 4 weeks

    measuring the size of the wound (W, L,H)

  3. Stride Length Difference Between Pulseflow Offflaoding and Standard Offloading

    Time frame: baseline

    the quality of walking while wearing Pulseflow offflaoding compared to standard offloading

  4. Limp Difference Between Pulseflow Offflaoding and Standard Offloading

    Time frame: baseline

    Limp: the difference in stance percent between right and left feet

  5. Peak Swing Angular Velocity

    Time frame: baseline

    Angular Velocity of leg swing during walking for each side

  6. Ratio of Propulsion Time to Stance Time

    Time frame: baseline

    Propulsion time and stance time for each stride is caulcated by wearable sensors. The measure is ratio of propulsion time to stance time as percentage value.

  7. Center of Mass Sway While Wearing Standard Offloading Boot

    Time frame: baseline

    Center of Mass (COM) sway measured by wearable inertial sensors

  8. Center of Mass Sway While Wearing Pulseflow Offloading

    Time frame: baseline

    center of mass sway measured by a wearable inertial sensor

  9. Peak Forefoot Pressure

    Time frame: baseline

Sponsors and collaborators

Lead sponsor

Baylor College of Medicine

Other

Collaborators

  • The Diabetic Boot Company

Registry information

Important dates

Study start
2016
Primary completion
2019
Study completion
2019
First posted
May 26, 2016
Registry last updated
Aug 12, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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