← Eichor
Study identifier: NCT06520150 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Evaluation of the Effectiveness of Two Methods of Regional Anesthesia During S-ICD Implantation Procedure.

Condition: Chest Pain · Pain, Procedural · Pain, Postoperative  ·  Sponsor: 4th Military Clinical Hospital with Polyclinic, Poland

PhaseNA
Planned participants32
Who can joinAll sexes, 18 Years to 90 Years
Healthy volunteersNo

About this study

Our study consists of a combination of regional blockade ('local' anesthesia) of the anterior and lateral chest wall in the form of a thin needle prick and the supply of local anesthetic drugs to the area of the relevant chest wall structures to exclude all stimuli, including pain from the operative site. A short-acting analgesic and sedative drug will be administered intravenously throughout the procedure - in a dose that allows the required contact between the patient and the anesthetist. If necessary, the dose of the drug may be increased to maintain pain comfort throughout the procedure. The anesthetic team will be with the patient throughout the procedure to ensure comfort and safety.

This description comes directly from the study's public registry record.

Talk to the study team

Marek Szamborski, MD  ·  698448639  ·  mszamborski@4wsk.pl

Always discuss trial participation with your own doctor first.

Locations (1)

4th Military Clinical Hospital with PolyclinicWroclaw, Lower Silesian Voivodeship, PolandRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06520150