Evaluate the Safety and Efficacy of RegenKit Autologous PRP Gel for the Treatment of Diabetic Foot Ulcer

RegenLab

Status

Unknown

Conditions

Diabetic Foot Ulcers

Treatments

Device: Placebo

Device: Autologous platelet rich plasma gel

Study type

Interventional

Funder types

Industry

Identifiers

NCT02402374

2014-WH-02

Details and patient eligibility

About

Autologous platelet-rich plasma (PRP) gel was reported to have very good outcomes in the treatment of foot ulcers in pilot studies and retrospective uncontrolled trials. Therefore, a larger randomized, placebo-controlled clinical trial will be useful to determine whether platelet-rich plasma is safe and effective for the treatment of diabetic foot ulcers (DFU).

Full description

Evaluate the safety and efficacy of RegenKit autologous PRP Gel for the treatment of diabetic foot ulcer is a randomized, placebo controlled, blind-assessor study. One hundred and seventy four patients will be treated, 87 patients receiving treatment arm and 87 patients receiving placebo. The primary endpoint is to evaluate proportion of patients with complete wound closure at week 16 when treated with autologous platelet rich plasma gel compared to the proportion of control (saline gel) treated patients with complete wound closure at the same time-point.

Enrollment

192 estimated patients

Sex

All

Ages

18 to 95 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria

Patients who in the opinion of the Investigator, are capable of understanding and complying with protocol requirements
Patients or, when applicable, their legal representatives, sign and dates a written IFC and/or any required privacy authorization prior to the initiation of any study procedure
Patients aged 18 to 95 (inclusive) with Type 1 or Type 2 diabetes undergoing therapy for glycemic control
Patients with glycated hemoglobin (HbA1C) less than or equal to 12%
Patients having ulcers which meet the following criteria:
Ulcer should not be infected as determined by clinical examination
Ulcer duration of 4 weeks or longer
Ulcer area (length x width) of between 1.5 cm2 and 20 cm2
Full-thickness ulcer of Grade 1 or Grade 2 as per Wagner's classification system
Ulcer has undergone recent debridement (2 weeks prior to screening)
Post-debridement ulcer is free of necrotic debris, foreign bodies, sinus tracts, tunneling, and undermining and is comprised of healthy vascularized tissue
Patients with Charcot deformity, the wound should be free of acute changes and, in the opinion of Investigator, should have undergone appropriate structural consolidation (the affected charcot fractures will have been fused together and should be sufficiently stable to allow the patient to weight-bear)
Patients having adequate circulation to the foot as documented by either:
1. Ankle Brachial Index (ABI) between 0.60 and 1.30, or
2. Patients with falsely elevated ABI values (equal to or greater than 1.30) due to non-compressible ankle vessels:
i)Toe Brachial Index (TBI) equal to or greater than 0.50 or, ii)TBI is not available (toe is absent, wounds are present, or investigative site cannot perform a TBI), a Doppler waveform in the posterior tibial or dorsalis pedis arteries at the ankle consistent with adequate flow in the foot (biphasic or triphasic) and other diagnostic confirmation of adequate flow (e.g duplex imaging or normal pulse volume recording)
Patients who agree to conform to the off-loading requirements
Patients of childbearing age must agree to use a method of contraception or agree to abstain from sexual intercourse throughout the study

Exclusion Criteria

Patients with ulcers having an active infection with/without purulent discharge
Patients with ulcers with exposed bone or associated with osteomyelitis
Patients with target limb cellulitis, or ischemic or gangrenous ulcers
Patients who have undergone, in the 2-week period prior to enrollment, treatment for DFU with any advanced treatment modality other than standard of care, such as growth factors, skin substitutes or other biological treatments
Female patients who are pregnant or lactating
Patients diagnosed with cancer, undergoing chemotherapy, except basal cell carcinoma
Patients with wounds caused by basal cell carcinoma or due to basal cell carcinoma excision
Patients with wounds due to malignancy
Patients having had any revascularization surgery within the 4-week period prior to signing the ICF
Patients with renal failure requiring dialysis
Patients with platelet count outside of the normal range of 150-400 x 1000/uL
Patients with a history of allergy to one of tested components
Patients with a history of bleeding disorders
Patients suffering from skin or blood cancers, or having suffered in the past from such cancers and not having, certification of a total remission
Patients presenting skin lesions potentially caused by abnormal cellular proliferation process (history of being cancerous)
Patients with a history of any condition, physical examination finding, or clinical laboratory finding, giving reasonable suspicion of a disease or condition that contraindicates the use of the investigational agent or may confound the interpretation of study results or might render the patient at high risk for treatment complications
Patients with active Charcot or other structural deformity that would prevent adequate off-loading of the study foot