Informazioni generali
  • Categoria della malattia Altro (BASEC)
  • Stato di reclutamento reclutamento non ancora iniziato (BASEC/ICTRP)
  • Luogo dello studio
    Bellinzona
    (BASEC)
  • Responsabile dello studio Dr. med. Roberto Dossi roberto.dossi@eoc.ch (BASEC)
  • Fonte dati BASEC: Importato da 02.06.2025 ICTRP: N/A
  • Ultimo aggiornamento 02.06.2025 18:10
HumRes66957 | SNCTP000006427 | BASEC2025-D0048

Real-time monitoring of local anesthetic injection pressure during peripheral loco-regional anesthesia

  • Categoria della malattia Altro (BASEC)
  • Stato di reclutamento reclutamento non ancora iniziato (BASEC/ICTRP)
  • Luogo dello studio
    Bellinzona
    (BASEC)
  • Responsabile dello studio Dr. med. Roberto Dossi roberto.dossi@eoc.ch (BASEC)
  • Fonte dati BASEC: Importato da 02.06.2025 ICTRP: N/A
  • Ultimo aggiornamento 02.06.2025 18:10

Descrizione riassuntiva dello studio

Several studies have shown that an increase in local anesthetic injection pressure may indicate incorrect positioning of the needle tip, within a nerve or a vessel, or accidental contact between the needle and nerve. The use of a medical device that allows continuous and real-time monitoring of injection pressure during loco-regional anesthesia could help achieve a more effective and safer injection. In this trial, we examine whether the new medical device Smart Needle Monitoring System is effective and safe. The Smart Needle Monitoring System consists of a standard needle, used in clinical practice for performing loco-regional anesthesia, within which a sensor is incorporated that measures the injection pressure at the needle tip. The needle is connected to a screen that allows visualization and recording of the local anesthetic injection pressure. In the event of a sudden increase in injection pressure, the anesthetist can immediately stop the injection, reposition the needle, and restart. In this trial, patients undergoing surgery below the elbow (of the hand, forearm, etc.) under ultrasound-guided peripheral loco-regional anesthesia via the axilla are randomly divided into 2 groups. In both groups, the standard needle of the Smart Needle Monitoring System is used to inject the anesthetic. Each group undergoes a different intervention: in the experimental group, the anesthetist visualizes and controls the injection pressure in real-time on the screen connected to the needle, while in the control group, the anesthetist injects the anesthetic without visualizing and controlling the injection pressure in real-time, as is done in standard clinical practice. Participation involves 3 visits (1 hospital visit for the surgical procedure plus 2 phone interviews for post-operative evaluation) and lasts for 8 days.

(BASEC)

Intervento studiato

In the experimental group, the Smart Needle Monitoring System medical device is used to perform ultrasound-guided axillary loco-regional anesthesia. The anesthetist uses the standard needle of the Smart Needle Monitoring System to inject the local anesthetic. The screen connected to the needle displays in real-time and records the injection pressure profile during anesthesia. The anesthetist will use real-time visual feedback to maintain low injection pressure and avoid pressure spikes.

In the control group, the Smart Needle Monitoring System medical device is used to perform ultrasound-guided axillary loco-regional anesthesia. The anesthetist uses the standard needle of the Smart Needle Monitoring System to inject the local anesthetic. Unlike the experimental group, the screen connected to the needle will be rotated, allowing for the recording of injection pressure but not real-time visualization by the anesthetist, who will perform the procedure as usual in standard clinical practice without visual feedback of the injection pressure.

(BASEC)

Malattie studiate

Surgery below the elbow (e.g., hand surgery, forearm surgery, etc.) under ultrasound-guided peripheral loco-regional anesthesia via the axilla

(BASEC)

Criteri di partecipazione
- Signed informed consent - 18 years or older - Surgical intervention below the elbow (e.g., hand surgery, distal radius surgery, forearm surgery) requiring axillary block - Physical condition suitable for anesthesia and surgery (ASA I-III) - Ability to understand the trial - Ability and willingness to follow and complete the trial procedures (BASEC)

Criteri di esclusione
- Contraindications to axillary block (e.g., local infection) - Refusal of loco-regional anesthesia for the surgical procedure - Pre-existing neurological damage in the arm to be operated on - Body mass index ≥ 35 kg/m2 - Known allergy to local anesthetic - Inability to perform post-operative evaluations (BASEC)

Luogo dello studio

Bellinzona

(BASEC)

non disponibile

Sponsor

Servizio di Anestesiologia, Ospedale Regionale di Bellinzona e Valli EOC, sede San Giovanni.

(BASEC)

Contatto per ulteriori informazioni sullo studio

Persona di contatto in Svizzera

Dr. med. Roberto Dossi

+41 91 811 9341

roberto.dossi@eoc.ch

Ospedale Regionale di Bellinzona e Valli EOC, sede San Giovanni

(BASEC)

Informazioni scientifiche

non disponibile

Nome del comitato etico approvante (per studi multicentrici solo il comitato principale)

Commissione d'etica Ticino

(BASEC)

Data di approvazione del comitato etico

02.06.2025

(BASEC)


ID di studio ICTRP
non disponibile

Titolo ufficiale (approvato dal comitato etico)
A Single-Center, First-in-Human, Randomized, Controlled, Feasibility Study of a New Device for the Real-Time Continuous Monitoring of the Injection Pressure of Local Anesthetic in Subjects Undergoing Ultrasound-guided Peripheral Nerve Block: the Smart Needle Monitoring System Investigation (BASEC)

Titolo accademico
non disponibile

Titolo pubblico
non disponibile

Malattie studiate
non disponibile

Intervento studiato
non disponibile

Tipo di studio
non disponibile

Disegno dello studio
non disponibile

Criteri di inclusione/esclusione
non disponibile

non disponibile

Endpoint primari e secondari
non disponibile

non disponibile

Data di registrazione
non disponibile

Inclusione del primo partecipante
non disponibile

Sponsor secondari
non disponibile

Contatti aggiuntivi
non disponibile

ID secondari
non disponibile

Risultati-Dati individuali dei partecipanti
non disponibile

Ulteriori informazioni sullo studio
non disponibile

Risultati dello studio

Riepilogo dei risultati

non disponibile

Link ai risultati nel registro primario

non disponibile