Non-healing Wounds Clinical Trial
Official 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.
Verified date | September 2023 |
Source | Inotec AMD Limited |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
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.
Status | Completed |
Enrollment | 8 |
Est. completion date | May 15, 2022 |
Est. primary completion date | May 15, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
United States | Salem VA Healthcare | Roanoke | Virginia |
Lead Sponsor | Collaborator |
---|---|
Inotec AMD Limited | Salem VA Medical Center |
United States,
4. Lordish, H. (2000) Molecular cell biology, Freeman, New York.
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Effectiveness 0f remote management and telehealth | Change in number of face to face clinic visits necessary | 12 weeks | |
Primary | Number of participants that achieve complete wound closure. | Percentage change in ulcer size relative to baseline measurement | 12 weeks |
Status | Clinical Trial | Phase | |
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Completed |
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