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Completed

NCT Number: NCT04746573

Effect of Natrox Oxygen Wound Therapy on Non-healing Wounds and Implication of Remote Monitoring and Telehealth for Management in the Home.

Single center pilot study examining the effect of Natrox topical oxygen therapy on chronic wounds along with the introduction of remote monitoring and telehealth for home care management.

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Key information

About this study

There is a wealth of evidence to support the benefits of oxygen therapy on wound healing. Oxygen is required for all major processes of wound healing and wound hypoxia is common. Skin wounds can receive oxygen from the blood stream via perfusion and from oxygen uptake through the skin. Yet, both wound perfusion and blood oxygen levels are frequently insufficient in patients with chronic wounds due to poor circulation, vascular disruption, and vasoconstriction, thereby reducing the wound's capacity to heal.

Diabetic ulcers, vascular ulcers (venous or arterial), and pressure injuries are all chronic wounds. The pathologies underlying chronic wounds can differ widely. However, common shared features include prolonged or excessive inflammation, persistent infections, and the inability to respond to reparative stimuli. Adults with vascular disease and/or diabetes are at highest risk for chronic leg and foot wounds. The ischemic (reduced tissue perfusion) and/ or hypoxic lower limb conditions which result from these conditions reduces availability of both oxygen and nutrients, making these wounds especially hard to heal. These wounds last on average 12 to 13 months, but this varies widely; many will remain open for years or never heal, and up to 30% of DFUs go onto amputation. Even when they do heal, wounds recur in 60-70% of patients, decrease quality of life, and are a significant cause of morbidity.

The need for telehealth and remote patient monitoring in the current climate is critical and reinforces the VA's strategy to protect and care for Veterans, their families, heath care providers and staff in the face of this pandemic.

The VA's tactic to shift outpatient care to a "telehealth" mode, with phone, video and/or electronic communication to meet the needs of the ambulatory patient is difficult to achieve in wound care as clinicians rely heavily on the visual appearance of the wound to direct their therapy decisions. Thus, it is imperative to validate a remote monitoring tool that offers standard telehealth care as well as accurate, consistent, and simple wound measurement and imagery. Having the ability to manage complex wounds accurately should enable quick identification of early warning signs that the wound is deteriorating thus facilitating appropriate triaging of patients that need urgent face to face medical review.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Subject having non-healing wound of any etiology except for 3rd degree burns
  • No visible improvement in the previous 4 weeks.
  • Wound present for at least 4 weeks but less than 12 months.
  • Subjects wound is not less that 1 cm sq or greater than 25 cm sq
  • Subject is able and willing to participate in self care
  • Subject is able and willing to follow protocol requirements
  • Subject has signed informed consent

Exclusion criteria

  • Subject has life expectancy of <1 year
  • Subject is unable to manage the Natrox device.
  • Subject unable or reluctant to use Iphone and imaging technology
  • Subjects ulcers are 100% necrotic or if physician felt it necessary to completely cover the wound with creams or gels that would prevent the transmission of oxygen to the wound base.
  • Subject has major uncontrolled medical disorder(s) such as serious cardiovascular, renal, liver or pulmonary disease, lupus, palliative care or sickle cell anemia.
  • Subject is currently being treated for active malignant disease or patients with history of malignancy within the wound
  • Subject has other concurrent conditions that in the opinion of the investigator may compromise subject safety
  • Known contraindications to Natrox
  • Known allergies to any fo the Natrox components
  • Known allergies to adhesives

Treatment and study plan

Natrox Topical Oxygen Therapy

Device

Device delivering humidified oxygen directly to the wound bed

Primary outcomes

  1. Number of participants that achieve complete wound closure.

    Time frame: 12 weeks

    Percentage change in ulcer size relative to baseline measurement

Other outcomes

  1. Effectiveness 0f remote management and telehealth

    Time frame: 12 weeks

    Change in number of face to face clinic visits necessary

Sponsors and collaborators

Lead sponsor

Inotec AMD Limited

Industry

Collaborators

  • Salem VA Medical Center

Registry information

Official study title

A Single Center Pilot Study to Examine the Effect of NATROX Oxygen Wound Therapy on Non-healing Wounds and the Practical Implication of Introducing a Remote Monitoring and Telehealth Solution to Manage These Complex Patients in the Home Setting.

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Feb 10, 2021
Registry last updated
Sep 28, 2023

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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