Clinical Trial

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

Unknown
View on ClinicalTrials.gov →
Record status
This record was last updated July 25, 2024 (before its estimated December 1, 2025 completion). Its status may not reflect the trial's current state.
Summary
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.
Protocol Amendment History 1 change
critical Trial status changed: Recruiting → Unknown 2026-08-02
Trial Details
NCT Number NCT06520150
Lead Sponsor 4th Military Clinical Hospital with Polyclinic, Poland
Conditions Chest Pain, Pain, Procedural, Pain, Postoperative, Analgesia, Regional Anesthesia Morbidity, Anesthesia, Local, ICD
Enrollment 32 participants
Start Date 2024-06-16
Primary Completion 2025-12-01 (estimated)
Study Completion 2025-12-01 (estimated)
Updated on ClinicalTrials.gov 2024-07-25