Evaluation of Topical Wound Oxygen (two2) Therapy

NCT ID: NCT00871312

Last Updated: 2014-01-10

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 21 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2007-05-31
• Study Completion Date: 2009-12-31

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.

Conditions

Diabetic Ulcer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Topical Wound Oxygen Therapy

Subjects will receive four 90 minute treatments of two2 therapy per week

Group Type: ACTIVE_COMPARATOR

Topical wound oxygen therapy

Intervention Type: DEVICE

90 minutes 4 days per week Active Topical Oxygen Therapy

Placebo Therapy

Subjects will receive four 90 minute treatments of Placebo two2 therapy per week

Group Type: PLACEBO_COMPARATOR

Topical wound oxygen Placebo

Intervention Type: DEVICE

90 mins per day 4 days per week Placebo Therapy

Interventions

Topical wound oxygen therapy

90 minutes 4 days per week Active Topical Oxygen Therapy

Intervention Type: DEVICE

Topical wound oxygen Placebo

90 mins per day 4 days per week Placebo Therapy

Intervention Type: DEVICE

Eligibility Criteria

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 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.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

AOTI Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Laura E Edsberg, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

Daamen College

Locations

AOTI Clinic

Buffalo, New York, United States

Community Dermatology & Wound Healing Clinic

Mississauga, Ontario, Canada

Wound Care Clinic

Saint Catherines, Ontario, Canada

Countries

United States; Canada

Other Identifiers

AOTI-001

Identifier Type: -

Identifier Source: org_study_id