Safety Trial of the RedDress Wound Care System (RD1) in Management of Texas 1a or 2a Neuropathic Diabetic Foot Ulcers.
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT01396837|
Recruitment Status : Completed
First Posted : July 19, 2011
Last Update Posted : April 17, 2017
|Condition or disease||Intervention/treatment||Phase|
|Neuropathic Diabetic Ulcer - Foot||Device: RedDress Wound Care System (RD1)||Phase 2|
The investigational product, the RD1 kit, was designed to enable a care provider to create an in vitro blood clot from the patient's own blood at the point of care, in a safe and effective manner.
While many advanced modalities of treatment have been developed to heal chronic DFUs (as well as other types of chronic wounds), the vast majority have been approved for relatively non-severe wounds (e.g., Texas 1a/2a grades) and relatively healthy subjects in controlled clinical trials and typically exclude 25-75% of subjects who have several comorbidities and severe wounds. Moreover, when the results of such trials (and other trials of advanced modalities) have been subject to a systematic review, the strength of the evidence for their efficacy has been rated low or even insufficient to judge. Consequently, there is an urgent need for new technologies to be tested that can improve healing rates in all classes of chronic DFUs.
The study is a multi-center, prospective, single group safety study, consisting of 20 subjects who will complete the study (note: if any patients are lost to follow-up or withdrawn, enrollment will increase to compensate for loss of these subjects). The subjects will receive 12 weekly RD1 applications. Subject data will be kept in each site's records.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||20 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||A Multi-Center, Prospective, Open Label Safety Trial of the RedDress Wound Care System (RD1) in Management of Texas 1a or 2a Neuropathic Diabetic Foot Ulcers.|
|Actual Study Start Date :||May 2014|
|Primary Completion Date :||August 2016|
|Study Completion Date :||March 2017|
Experimental: RedDress Wound Care System (RD1)
RD1 is a biologic autologous wound care product which is comprised of the patient whole blood and produced in the point of care using the RD1 kit
Device: RedDress Wound Care System (RD1)
Weekly application. A blood based wound care treatment
- Adverse event rate [ Time Frame: 12 weeks ]Adverse event rate will be calculated including serious adverse events (SAEs), adverse events (AEs) (including any lack of venous access events), and device-related adverse events (DRAEs) (safety population and ITT populations).
- Complication rate due to lack of venous access [ Time Frame: 12 weeks ]for all patients for all 12 visits involving RD1 procedure (ITT population)
- Complication rate due to lack of venous access [ Time Frame: 12 ]for all patients for all 12 visits involving other procedure requiring venous access (ITT population)
- Incidence of complete wound closure at 12 weeks [ Time Frame: 12 weeks ]Defined as skin re-epithelialization without drainage or dressing requirements confirmed at 2 consecutive study visits 2 weeks apart) for DFU treated with RD1 (ITT population).
- Percent reduction in wound size over 12 weeks (ITT population) [ Time Frame: 12 weeks ]The data will also be plotted graphically week by week. Week 12 data will be used to recalculate sample size for the pivotal trial
- Associations between lack of healing and patient/wound parameters (ITT population) [ Time Frame: 2 years ]A simple Cox regression will be used to examine each wound and patient parameter. Note: because sample size is very small, a full Cox regression cannot be undertaken.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01396837
|United States, Florida|
|Miami, Florida, United States, 33185|
|Barry University Clinical Research|
|North Miami Beach, Florida, United States, 33169|
|United States, Pennsylvania|
|SerenaGroup Research Institute|
|Pittsburgh, Pennsylvania, United States, 15222|
|Martin Foot and Ankle|
|York, Pennsylvania, United States, 17402|