Evaluation of the Effectiveness of Two Methods of Regional Anesthesia During S-ICD Implantation Procedure.
Recruiting
N/A
Interventional Study
Chest Pain
Pain, Procedural
Pain, Postoperative
Analgesia
Regional Anesthesia Morbidity
Anesthesia, Local
ICD
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 90
- Sex
- Any
- Study type
- Interventional
- Purpose
- Screening
- Participants needed
- 32 (estimated)
- Sponsor
- 4th Military Clinical Hospital with Polyclinic, Poland · Other
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About This Trial
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 …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* patients aged 18-90 years requiring S-ICD implantation for cardiac indications,
* high risk of anesthesia (ASA II or higher), patients giving informed consent to participate in the study.
Exclusion Criteria:
* absolute contraindications to regional anesthesia such as general…
Contacts