Evaluation of Topical Wound Oxygen (two2) Therapy

Not Applicable

Terminated

• Conditions: Diabetic Ulcer
• Interventions: Device: Topical wound oxygen therapy; Device: Topical wound oxygen Placebo

• Registration Number: NCT00871312
• Lead Sponsor: AOTI Ltd.

Brief Summary

The purpose of this study is to evaluate the efficacy of the Topical Wound Oxygen (two2) therapy system on the healing of diabetic lower extremity ulcers.

Detailed Description

The AOTI two2 therapy trial is a randomized, double-blinded, parallel group, placebo-controlled, multi-center study intended to evaluate the efficacy of Topical Wound Oxygen (two2) therapy in relation to placebo when added to standard of care in the treatment of diabetic lower extremity ulcers.

Study Timeline

• Study Start: 2007-05
• Study First Submitted: 2009-03-26
• Study First Submitted QC: 2009-03-27
• Study First Posted: 2009-03-30
• Primary Completion: 2009-12
• Study Completion: 2009-12
• Status Verified: 2014-01
• Last Update Submitted: 2014-01-08
• Last Update Posted: 2014-01-10

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 21

Inclusion Criteria

• Subject or legal representative has read, understands, and has signed the Institutional Review Board (IRB)-approved Informed COnsent Form (ICF) prior to enrollment in the study;
• Subject is 18 years of age or older;
• Subject has a current diagnosis of Type I or Type II diabetes mellitus;
• Subject has a diabetic lower extremity ulcer;
• Subject's index ulcer is at least 1.0cm2 in area;
• Subject's index ulcer is a superficial, partial or full thickness skin ulcer (Wagner Classification System I, II or III) which has been present for at least 4 weeks at the time of initial screening that has not improved with standard of care;
• Subject's index ulcer appears to be free of sinus tracts and tunneling;
• Subject's index ulcer exhibits no signs of moderate or severe clinical infection;
• In the event of multiple wounds on the same foot, the index ulcer will be the largest ulcer meeting the other inclusion criteria;
• In the event of multiple wounds on the same foor, the index ulcer is at least 2 cm from any additional wound edge;
• Women of childbearing potential must not be pregnant or lactating;
• Subject and/or caregiver are willing and able to comply with all specified care and visit requirements, and subject has a reasonable expectation of completing the study;
• Subject must be fit to undertake the study trial in the opinion of the referring doctor
• Subject's Great Toe pressure is greater than 20mmHg.

Exclusion Criteria

• Subject is currently enrolled in another investigational device or drug trial, or has been previously enrolled in investigative research for a device or pharmaceutical agent within the last 30 days;
• Subject's index ulcer has gangrene or gangrene is located on any part of the foot with the index ulcer;
• Subject has an acute and/or active Deep Vein Thrombosis;
• Subject is currently receiving or has received in the last six (6) months radiation or chemotherapy;
• Subject has received growth factor therapy within seven (7) days prior to initial screening;
• Subject has a significant medical condition that would impair wound healing, for example: severe liver disease, aplastic anemia, scleroderma, malnutrition, malignancy, etc;
• Subject has known or suspected osteomyelitis;
• Other than debridement, the underlying wound pathology requires surgical correction for the index ulcer to heal;
• Subject is receiving or has received corticosteroids (all applications), immunosuppressive agents, or other drugs that would impair wound healing within seven (7) days prior to initial screening or is anticipated to require them during the course of the study;
• Subject has an acute or active Charcot foot per clinical and radiology results or significant bony prominences that would preclude adequate off-loading with the standard off-loading device. The presence of Charcot foot in itself does not exclude the subject;
• Subject has known HIV, hepatitis, active cancer (except basal cell and non-melanoma skin cancer), or a bleeding disorder;
• Subject is undergoing renal dialysis;
• Subject suffers from known alcohol or drug abuse;
• Use of the standard off-loading device is contra-indicated or cannot be appropriately fitted to the subject.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Topical Wound Oxygen Therapy	Topical wound oxygen therapy	Subjects will receive four 90 minute treatments of two2 therapy per week
Placebo Therapy	Topical wound oxygen Placebo	Subjects will receive four 90 minute treatments of Placebo two2 therapy per week

Primary Outcome Measures

Name	Time	Method
Wound closure	12 Weeks

Secondary Outcome Measures

Name	Time	Method
The time to wound closure	Variable
The type and amount of wound drainage or exudates	4, 8 and 12 weeks
The level of wound pain	4, 8 and 12 weeks
The degree of wound closure	4, 8, and 12 weeks
The percentage of tissue types	4, 8 and 12 weeks

Trial Locations

Locations (3)

Community Dermatology & Wound Healing Clinic; 🇨🇦 Mississauga, Ontario, Canada

Wound Care Clinic; 🇨🇦 St. Catherines, Ontario, Canada

AOTI Clinic; 🇺🇸 Buffalo, New York, United States