Evaluate the Reconstruction of Digital Nerve Defects in Humans Using an Implanted Silk Nerve Guide
- Conditions
- Peripheral Nerve Injury Digital Nerve Hand
- Interventions
- Device: SilkBridge
- Registration Number
- NCT03673449
- Lead Sponsor
- Silk Biomaterials srl
- Brief Summary
The goal of this study is to ascertain the feasibility and safety of the procedure using SilkBridge - a biocompatible silk fibroin-based scaffold - for the regeneration of sensory nerve fibres and follow it up together with the reinnervation of the target organs (sensory receptors in the skin).
- Detailed Description
This is a pre-market, monocentre, first-in-human pilot on adult patients with digital nerve defects. Category C clinical trial, medical devices. The study will be performed in Switzerland.
SilkBridge is a biocompatible silk fibroin-based scaffold, which recruits the patients' own cells to remodel or regenerate the nerve, without pre-seeding of the scaffold nor biological/chemical treatments.
SilkBridge will provide surgeons with an implant with unique features, such as easy suturability, full biocompatibility and specific biomimetic properties that enhance cells adhesion and integration of the device with the surrounding tissue.
The study will have a 12 months and 1 week duration per patient, including the follow-up period, and with an expected enrollment period of 15 months.
The study will evaluate 15 adult patients, aged 18-65 years, diagnosed with digital nerve defects (\> 5 mm gap) in whom surgical repair may not allow direct suture.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 4
- male & female patients between 18 and 65 years of age
- a traumatic injury or a post-traumatic neuroma of a digital nerve on the palmar side of the hand, between the metacarpophalangeal joint and the distal interphalangeal joint
- single lesion per finger
- nerve defect of >5mm
- nerve treatment initiated within 24 months after nerve injury
- signed informed consent
- disorders known to affect the peripheral nervous system, such as, but not only, diabetes mellitus, chronic heavy alcohol use, or toxic nerve lesions, or any polyneuropathy
- an additional injury that could compromise nerve regeneration
- clinically significant (as defined by the investigator) renal, hepatic, cardiac, endocrine, metabolic, hematologic, autoimmune, or any systemic disease, which may make implementation/interpretation of the protocol or results difficult
- previous conditions of the hand that could affect the healing of the actual nerve injury
- complete amputation injury
- extensive crush injury
- grossly contaminated wound
- receiving immunosuppressive or antineoplastic agents within 30 days prior to the enrolment
- known to be HIV positive
- known pregnant and lactating females
- participated in another clinical investigation using an investigational new drug or device (or in the present study) within 30 days prior to enrolment into this investigation
- uncooperative or unsuitable, e.g. language problems or a suspicion to be unable to attend follow up appointments, for completion of the investigation
- absence of a healthy opposite finger
- suspected allergy to silk
- need of emergency surgery (within 24 hours from injury)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description SilkBridge treatment SilkBridge Surgery for digital nerve reconstruction with SilkBridge
- Primary Outcome Measures
Name Time Method Safety of SilkBridge 12 months Assess type and severity of adverse device effects related to SilkBridge and surgical procedure throughout the follow-up period
- Secondary Outcome Measures
Name Time Method Performance - assess at the last visit 12 months Patient's satisfaction through the Patient Global Impression of Change (PGIC) questionnaire (Patient has to describe the change (if any) in activity limitations, symptoms, emotions and overall quality of life, in relation to its painful condition. 0 value represent no change, 7 a considerable improvement).
Performance - assess at each study visit versus baseline 12 months Sensory recovery after nerve reconstruction by static and moving 2-point discrimination and Semmes-Weinstein monofilament testing Pain evaluation via a visual analog scale (VAS: scale where patient has to specify level of pain by indicating a position along a continuous line between two end-points (0 - 10). 0 indicates no pain while 10 represents the highest level.)
Performance - assess at V5 and at last visit versus opposite control finger 6 and 12 months Sensory recovery by static and moving 2-point discrimination and Semmes-Weinstein monofilament testing
Trial Locations
- Locations (1)
Klinik für Plastische Chirurgie und Handchirurgie - UniversitätsSpital Zürich
🇨🇭Zürich, Switzerland