Safety Evaluation of the KLOX BioPhotonic System in Stage II and III Pressure Ulcers

Klox Technologies

Status

Completed

Conditions

Pressure Ulcers Stage III

Pressure Ulcers Stage II

Treatments

Device: KLOX BioPhotonic System

Study type

Interventional

Funder types

Industry

Identifiers

NCT02222454

CL-K1002-P006

Details and patient eligibility

About

The primary objective of these case series is to evaluate the safety and tolerability of the KLOX BioPhotonic System as adjunctive therapy to Standard Of Care (SOC) in patients with stage II or III pressure ulcers.

Enrollment

3 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Male or female 18 years of age and older;
The subject or legal guardian must have signed an informed consent form;
Female of child bearing potential must have a negative pregnancy test result at Baseline and both male and female patients must be willing to adhere to a medically-accepted birth control method during the course of the study;
Willingness to return for all study visits;
Stage II or III pressure ulcer (as per NPUAP Staging Guidelines), present for more than 4 weeks (up to Screening visit), located in the ischial, trochanteric, coccygeal, thoracic or abdominal regions. Lower extremity pressure ulcers, such as heel ulcers, are acceptable provided that diabetic foot ulcers are ruled out if the patient has diabetes. Surface dimensions of ulcer must be between 2 to 64 cm2 inclusive but longest diameter must not exceed 10 cm. Depth must not exceed 5 cm;
Wound area has not changed by more than +/- 30% between Screening visit and Week 1/Visit 1 (before treatment).

Exclusion criteria

Pressure ulcer present for more than 18 months;
The ulcer to be treated is planned for operative debridement;
The ulcer has significant necrotic tissue (e.g., more than 20% of the ulcer area);
Major uncontrolled medical disorder(s) such as serious cardiovascular, renal, liver or pulmonary disease, lupus, palliative care or sickle cell anemia;
Severe or significant hypoalbuminemia (albuminemia < 30 g/L, and/or pre-albumin < 5 mg/dL), or hypoproteinemia (proteinemia < 55g/L);
Patient with moderate to severe anemia (Hb < 90g/L);
Patient currently treated for an active malignant disease;
Patient with history of malignancy within the wound;
Patient with history of radiation therapy to the wound region;
Patient with prior diagnosis of active malignant disease who is less than 1 year disease-free;
Patient with a known osteomyelitis or active cellulitis;
Patients that are immunosuppressed or on high dose chronic steroid use;
Patients on systemic corticosteroids (a completion of corticosteroid course at least 30 days prior to study enrolment is required);
Patient with active or systemic infection (note that the patient is however eligible for re-screening after the systemic infection has subsided);
Patients with severely uncontrolled diabetes mellitus (defined as A1C > 12%);
Dermatologic comorbid disease (e.g., cutis laxa or collagen vascular disease);
Active bleeding;
Pregnancy, or breast feeding;
Patients with bleeding diathesis;
Patients on Warfarin or IV Heparin;
The subject has any physical or psychiatric condition that in the Investigator's opinion would warrant exclusion from the study or prevent the subject from completing the study (e.g., severe morbid obesity, recent hip fracture, suspected non-compliance, etc.);
Patients with ulcers from burns (from exposure to high heat), venous ulcers or diabetic foot ulcers;
Concurrent disease or drugs known to induce severe photosensitivity of the skin, such as porphyria;
Patient has received biological-based therapy in any wound within 3 months of Screening;
Concurrent participation in another clinical trial that involves an investigational drug or device that wound interfere with this study;
Previous participation in other interventional wound healing clinical investigation within the 60 days prior to Screening visit.