Chronic Pain
Conditions
Brief summary
The EpiFinder device, which is the investigational device in this study, is intended for use in epidural procedures, between a luer syringe and an epidural needle, to give the treating physician a clear indication that the needle tip has entered the epidural space. The objective of this First In Human study is to evaluate the safety and performance of using the EpiFinder to identify the epidural space in subjects with a clinical indication to receive a lumbar Epidural Steroid Injections.
Interventions
DEVICEEpiFinder
The EpiFinder is a sensing device intended to assist physicians performing placement of epidural needle analgesic and/or anesthesia injection in a safely and accurately manner. The device is a single use sterile device consisting of a probe (Stylet), an actuator (micro DC motor), IR sensor and Controller. The device is integrated to a standard LOR Syringe and an 18G Tuohy needle and enables to simultaneously work with the standard LOR technique.
Sponsors
Omeq Medical
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Subject is 18 years or older * Subject with clinical indication for lumbar ESI based on subject's clinical problem (e.g. DDD hernia disc, spinal stenosis) * Subject understands the study requirements and the treatment procedures and provides written Informed Consent before any study-specific tests or procedures are performed
Exclusion criteria
* Subject with marked spinal deformities * Previous back surgery * Contraindication for epidural injections (e.g. continuous use of anticoagulants, infection, allergic reactions to the injected substances) * Subject has known hypersensitivity to contrast media that cannot be pre-medicated * Subject with severe obesity (body mass index \>35 kg/m2) * Subject observed seizure within 7 days prior to study enrollment * Subject presenting for emergency * Subject has a skin condition (i.e., hemangioma, scleroderma, psoriasis, rash, open wound or tattoo) in their lumbar region * Subject is pregnant (to be determined by urine pregnancy test) * Subject who is currently participating or has participated in an investigational study, within the past 30 days
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Safety - Device Related Serious Adverse Events | 14 days | cumulative incidence of device-related complications and Serious adverse events (AE), observed during the procedure and throughout the follow-up period. Device related adverse events include: dural puncture with or without headache, epidural hematoma, seizures, neurological deficit or relevant device complications. All related and non-related adverse events will be observed on a continuous basis from the baseline through the study completion. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Device Efficacy - Epidural Space Identification | Procedure | Ability of the physician to identify the epidural space using the EpiFinder. Once the device determines that the needle tip is in the epidural space, this position will then be confirmed by epidurography |
| Device Performance - Physician satisfaction | Procedure | physician's overall satisfaction from the device, as measured by a completion of an internal ease of use questionnaire. |
Countries
Israel
Contacts
Primary ContactMaya Shick
Backup ContactLior Margalit
Outcome results
None listed