Menu
Recruiting NCT06388629

Epicardial Access Study With Rook

No phase Interventional Arrythmia

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Rook Epicardial Access Kit.
Who it may be relevant to
Registry conditions: Arrythmia. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Czechia
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Epicardial Access Study With Rook (EASY-R)

Overview

The goal of this clinical trial is to test how how effective the Circa Scientific Rook® Epicardial Access Kit is at gaining guidewire access to the outside surface of the heart (epicardium). In addition the safety of the device will be compared to the available data for alternative methods of epicardial access. Participants will receive treatment with the subject device during the course of a typical epicardial electrophysiology procedure.

Detailed description

This trial is a confirmatory trial for the Circa Scientific Rook® Epicardial Access Kit for accessing the epicardial surface of the heart via a subxiphoid approach to facilitate guidewire placement into the pericardial space in adult patients. The purpose of this study is to confirm the safety and establish the efficacy of the Circa Scientific Rook® Epicardial Access Kit as a pericardial access device. The Rook® Epicardial Access Kit will be used to gain access the epicardial surface of the heart via a subxiphoid approach in adult patients with a normal, non-distended pericardial space.

Access success of the test device to the pericardial space and occurrence of CEC-adjudicated device and procedure related adverse events will be assessed in relation to complication rate existing data from the literature presenting epicardial access procedure results during subxiphoid (minimally invasive) surgical procedures. This is a prospective, single-arm, non-randomized study.

The primary endpoint is successful pericardial access through the use of the Circa Scientific Rook® Epicardial Access Kit, achieving guidewire access to the pericardial space as confirmed during the procedure by standard x-ray technique. The safety endpoint is the occurrence of CEC-adjudicated device or procedure related adverse events through hospital discharge or up to 4 days post procedure, whichever comes first. Additional endpoints include speed of access, ease of use and human factors data.

Interventions

  • Device Rook Epicardial Access Kit
    Access the epicardial surface of the heart via a subxiphoid approach with the subject device to facilitate guidewire placement into the pericardium.

Primary outcome measures

  • Successful Epicardial Access [Time frame: During procedure.]
Secondary outcome measures (2)
  • Speed of Access [Time frame: During procedure.]
  • Rate of Use Errors [Time frame: During procedure.]

Eligibility criteria

Inclusion criteria

  • Patient is clinically indicated to undergo a procedure that requires percutaneous access to the normal, non-distended, pericardial space.
  • Patient is willing and able to provide written informed consent.

Exclusion criteria

  • Subject is younger than 18 years of age
  • Previous cardiac surgery
  • Myocardial infarction within 4 weeks prior to procedure
  • Class IV NYHA (New York Heart Association) heart failure symptoms
  • Subject with an active systemic infection
  • Known carotid artery stenosis greater than 80%
  • Presence of thrombus in the left atrium
  • Congenital absence of a pericardium
  • Coagulopathy
  • Hemodynamic Instability
  • Acute conditions (i.e. electrolyte abnormality, acute ischemia, drug toxicity)
  • Severe hepatic dysfunction or enlargement
  • Subject has Body Mass Index > 40
  • Life expectancy less than 6 months
  • Subject is pregnant
  • Subject is currently participating in another investigational drug or device study that clinically interferes with the endpoints of this study
  • Subject has known or suspected allergy to contrast media
  • Subject is known to have pericardial fibrosis, pericardial adhesions, or prior failed epicardial access

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Other

Study locations

Czechia · 1 center
  • Na Homolce Hospital — Prague

Identifiers

NCT: NCT06388629 · M064-066 Rev 00

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗