RecruitingN/AOther

The Potential Protective Effect of Using Muscle Relaxants During Electroporation Ablation (PFA)

Sponsored by 4th Military Clinical Hospital with Polyclinic, Poland

NCT ID
NCT06707532
Target Enrollment
32 participants
Start Date
2024-08-01
Est. Completion
2025-12-01

About This Study

The study aims to improve the safety of the electroporation ablation (PFA) procedure by using muscle relaxants to reduce skeletal muscle damage during the procedure. It will also assess myocardial damage to improve the procedure's quality and speed up recovery after the procedure.

Conditions Studied

Kidney Failure, AcuteMyopathy; DrugsHeart ArrhythmiaSuccinylcholine SensitivityMuscle RelaxationGeneral Anesthetic Drug Adverse ReactionProjection

Interventions

  • Propofol
  • Rocuronium

Eligibility

Age:18 Years - 90 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* Patients with requirement for PFA ablation for cardiac indications and ability to provide informed consent for study participation

Exclusion Criteria:

* Patients with allergies to the general anaesthetics used, genetic diseases of the neuromuscular plateau - e.g. Duchenne dystrophy, myasthenia gravis - and patients who do not gived informed consent to participate in the study will be excluded from the study.

Study Locations (1)

4th Military Clinical Hospital with Polyclinic
Wroclaw, Lower Silesian Voivodeship, Poland

Interested in this trial?

Contact the study team to learn more about eligibility and enrollment.

Marek Szamborski, MD
CONTACT
698-448-639mszamborski@4wsk.pl
View on ClinicalTrials.gov
Data Source
ClinicalTrials.gov

Last updated from source

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