Evaluation of the SpinCare™ System in the Treatment of Partial Thickness Burns

Not Applicable

Completed

• Conditions: Partial Thickness Burn
• Interventions: Device: SpinCare

• Registration Number: NCT02997592
• Lead Sponsor: Nanomedic Technologies Ltd.

Brief Summary

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

Detailed 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

Study Timeline

• Study First Submitted: 2016-11-22
• Study First Submitted QC: 2016-12-19
• Study First Posted: 2016-12-20
• Study Start: 2017-03-20
• Primary Completion: 2021-03-09
• Study Completion: 2021-08-16
• Status Verified: 2022-06
• Last Update Submitted: 2022-06-12
• Last Update Posted: 2022-06-15

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 44

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
SpinCare	SpinCare	Patients with partial thickness burns treated with the SpinCare System

Primary Outcome Measures

Name	Time	Method
Burn wound healing	21 days	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.

Secondary Outcome Measures

Name	Time	Method
Dermal safety test (erythema and edema)	Every time the SpinCare dressing is delivered up to 21 days after initial dressing	Dermal safety will be assessed by Draize score including signs of erythema and edema.
Pain as assessed by VAS	21 days	Pain will be assessed at rest, during dressing application (when applicable) and during dressing removal (when applicable) using VAS (Visual Analog Scale) scale.
Number of participants having an infection at the burn wound.	Up to 21 days after initial application of the dressing	If infection is suspected clinically, a swab will be taken for microbiological examination and the patient will be treated according to the medical center's standard practice.
Ease of use	Every time the SpinCare is used up to 21 days after initial application of the dressing	ease of applying and removing the dressing will be evaluated using 0-5 numerical rating scale (NRS).

Trial Locations

Locations (3)

Burn Unit, Sheba Medical Center; 🇮🇱 Ramat Gan, Israel

Rambam Medical Center; 🇮🇱 Haifa, Israel

Sourasky Medical Center; 🇮🇱 Tel Aviv, Israel