Evaluation of the SpinCare™ System in the Treatment of Partial Thickness Burns (SPINCARE2)

Nanomedic Technologies

Status

Completed

Conditions

Partial Thickness Burn

Treatments

Device: SpinCare

Study type

Interventional

Funder types

Industry

Identifiers

NCT02997592

CIP0009

Details and patient eligibility

About

Evaluation of the SpinCare™ System in the Treatment of Partial Thickness Burns. A prospective, single arm, safety and efficacy, open labeled multi-center study

Full description

The SpinCare is an electrospinning portable device intended for the external treatment of burns and wounds. The SpinCare is the first made on the spot, bed side, and completely personalized dressing system; with excellent coverage of all size, shapes and difficult contours. The nano-fibrous dressing mimics the structure of natural body tissue and creates excellent medium for tissue repair and healing.

The objective of this study is to evaluate the performance, safety and efficacy of the SpinCare System in the treatment of superficial to intermediate partial thickness burns.

The study included 3 sites. Adult patients with superficial to intermediate partial thickness burns (second degree superficial to intermediate) of up to 10% TBSA (Total Body Surface Area); with an independent burn of up to 5% TBSA.

A prospective single arm, safety and efficacy, open labeled, multi-center study for the treatment of partial thickness burn wounds not considered for surgery using the SpinCare System.

44 patients enrolled in the study.

Endpoints:

Wound healing and re-epithelialization on day 21.
The burn will be considered healed when at least 95% of the total area is re-epithelialized and no scabs exist.
- Ease of use
- At postoperative days 7, 14, 21
Dermal safety assessed by Draize Score
Visual estimate of wound healing and re-epithelialization
Pain
Infection
Itching
- Itching and scar quality at 3 and 6 months
- Itching and scar quality at 12 months (optional)
- Device related adverse events

Enrollment

44 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients ≥ 18 years old at enrolment. Both genders.
The patient has partial thickness burn wounds (second degree superficial to intermediate) of up to 10% TBSA; of which the target wound for treatment is of up to 5% TBSA or up to 300cm2.
Presenting at the emergency room within the first 24-48 hours post-injury.
Patient's wound is defined as a partial thickness burn for conservative treatment (superficial to intermediate second degree).
Patient underwent cleansing/debridement of initial burn before applying the dressing
The patient is able and willing to comply with study procedures and give written informed consent prior to enrollment in the study

Exclusion criteria

Any known or suspected systemic infection
Any known sensitivity to components/products used in this study
Any active, uncontrolled, progressive or untreated malignancy
Use of penicillamine, corticosteroid or immunosuppressive medication within two months prior to enrollment or who is likely to be prescribed these medications or any other medications known to adversely affect wound healing during study participation
Major uncontrolled systemic disorders such as hepatic, renal, neurologic, or endocrinologic disorders
Major dermatological disorders such as: psoriasis, pemphigus, Steven Johnson, etc.
Patients with burns larger than 10% TBSA
Patients with burns up to 10% TBSA but no target wound of up to 5% TBSA or up to 300cm2
Patients suffering from electrical or chemical burns.
Patients suffering from frostbites.
Patients suffering from burn wounds that are third degree or full thickness.
Patients suffering from burn wounds in the head, neck or genital areas
Female patients who are pregnant or nursing
Psychiatric patient.
Soldiers
Participation in another clinical trial within 30 days prior to the Screening Visit