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RecruitingNCT06198933Updated Sep 19, 2024

Renal Function and Hemolysis After Pulsed-field Ablation for Atrial Fibrillation

An observational study in Atrial Fibrillation, sponsored by Charles University, Czech Republic. Recruiting at 1 site in Czech Republic. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-09-19.

Sponsored by Charles University, Czech Republic · Observational

From the registry’s dates

  • Primary completion was expected by Dec 2024, 1 year 10 months ago, but the record still lists the study as recruiting.
  • Started May 2024; still recruiting 2 years 6 months later.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
100
Ages
18 Years and older
Sex
All
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Study summary

The aim of the project is to assess hemolysis and renal function after catheter ablation for atrial fibrillation using pulsed-field energy. Hemolysis will be determined using the concentration of red blood cell microparticles at the end of the ablation (when all ablation were done, before sheath removal). Hemoglobinuria will be assessed one day after the procedure. Renal functions will be assessed one and three day after the procedure using standard parameters (creatinine, urea). The goal is to assess the acute worsening fo renal functions after pulsed-field ablation in relation to the number of PF applications, and to the degree of immediate post-procedural hemolysis.

Read the detailed description

Methods The project will include patients with paroxysmal and persistent AF who, according to standard recommended procedures, are indicated for catheter ablation using pulsed-field energy and will sign informed consent. Patients with spontaneously present hemolysis (hematologic disorders) and patients in a dialysis program will be excluded. The catheterization procedure will be performed routinely as currently practiced at our institution. Specifically, pulmonary vein isolation will be conducted in all patients, and for patients with non-paroxysmal AF, additional additive ablation lesions will also be performed (most commonly ablation of the posterior wall of the left atrium and mitral isthmus, possibly the cavotricuspid isthmus). The ablation will always be performed under moderate sedation or general anesthesia with the participation of an anesthesiologist, as per our institution's practice. A total of 100 patients are planned to be enrolled. Prior to the procedure, patients will receive at least 4 weeks of anticoagulant treatment with NOACs, as recommended, and this treatment will be discontinued on the day of the procedure (i.e., the last tablet will be taken the day before the procedure). NOACs will be reintroduced into their medication regimen the day after ablation. All patients will undergo outpatient baseline blood tests, including renal function (creatinine, urea), as currently standard and required (up to 2 weeks before the procedure). Post-procedure, patients will be adequately hydrated; in addition to the recommended active oral intake post-procedure, all patients will receive an extra 1000 ml of saline solution during the afternoon following the procedure (unless there is a risk of overhydration, for instance, in the case of severe dysfunction).

Blood sampling Blood samples will be collected at two different times. Firstly, at the end of the procedure, 12 ml of blood will be drawn into tubes for hemolysis examination (anticoagulated blood with EDTA and Li-heparin). The degree of hemolysis will be assessed by examining red blood cell fragments (RBC microparticles) using flow cytometry. This examination is highly sensitive and capable of detecting even minimal amounts of damaged erythrocytes. The second blood sample will be collected the morning after the procedure, following the standard protocol, and will also include renal parameters (creatinine, urea) as routinely done. Additionally, on this day, a urine test for the presence of hemoglobinuria will be conducted. Both initial blood samples will be collected and analyzed during the hospitalization. A third sample for a follow-up assessment of kidney function will be required 2-3 days after the procedure. The patient will be asked to come either to our hospital for blood collection or to have it done at a laboratory near their residence. Results of this examination, if conducted outside the hospital, will be obtained from the patient over the phone. If kidney function in this sample is slightly reduced, the patient will be instructed for further monitoring or outpatient examination. In case of significantly elevated values, appropriate action will be advised promptly.

Three months post-procedure, an outpatient check-up will be conducted. Before this evaluation, the effectiveness of the ablation will be assessed using a 24-hour ECG Holter monitor, which is our current standard procedure. Additionally, kidney function will be rechecked. The purpose is to compare the number of applications of pulsed-field energy with the degree of hemolysis observed immediately after the procedure, along with kidney function shortly after. Hemolysis, the damage or breakdown of red blood cells, will be determined using a highly sensitive method and is practically certain to be present at the end of the procedure. However, whether hemolysis might lead to hemoglobinuria the following day in some cases has not been investigated, nor has the potential for temporary worsening of kidney function in certain patients. If this were the case, selecting at-risk patients (those with higher creatinine levels before the procedure) and implementing simple measures (sufficient fluid intake) could effectively prevent this complication. Our primary hypothesis is that while ablation using pulsed-field is associated with intravascular hemolysis, leading to the damage of some red blood cells, this process in only a minimal number of patients will result in hemoglobinuria, and it will not have any significant consequences on kidney function post-procedure.

02

Conditions studied

  • Atrial Fibrillation

Keywords

  • atrial fibrillation
  • pulsed-fied ablation
  • hemolysis
  • renal function
03

In context

Atrial Fibrillation

4,009 studies on the registry are indexed under Atrial Fibrillation; 961 are open to participants now.

This study's planned enrollment of 100 is below the median of 300 across 1,400 observational studies indexed under Atrial Fibrillation.

Browse Atrial Fibrillation studies →

Lead sponsor

Charles University, Czech Republic is the lead sponsor of 228 studies on the registry; 76 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patient will symptomatic paroxysmal or non-paroxysmal atrial fibrillation indicated for catheter ablation according to the standard criteria will be enrolled.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • symptomatic paroxysmal or non-paroxysmal atrial fibrillation

Exclusion criteria

Exclusion Criteria:

  • known hematologic disorders
  • disorders associated with increased hemolysis
  • known significant hepatic disease
  • patient in permanent hemodialysis
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
100 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • Pulsed-field ablation group

    Patient with atrial fibrillation will undergo catheter ablation using pulsed-field energy

    Device: Pulsed-field ablation

Interventions

  • DevicePulsed-field ablation

    Patients will atrial fibrillation will undergo catheter ablation using pulsed-field energy

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What researchers measure

Primary outcomes

  1. Red blood cell microparticles

    The concentration of red blood cell microparticles in the plasma assessed using flow cytometry

    Time frame: day of the procedure - at the end of the procedure

  2. Hemoglobinuria

    The concentration of hemoglobin in urine

    Time frame: One day after the procedure

  3. Creatinine three days

    The concentration of creatinine three days after ablation

    Time frame: 3 days after the procedure

Secondary outcomes

  1. Lactate dehydrogenase

    The concentration of lactate dehydrogenase at the end of ablation

    Time frame: the day of the procedure - at the end of the procedure

  2. Haptoglobin

    The concentration of haptoglobin at the end of ablation

    Time frame: the day of the procedure - at the end of the procedure

  3. Creatinine one day

    The concentration of creatinine one day after ablation

    Time frame: one day after the procedure

07

Study locations

1 of 1 sites recruiting
  • Cardiocenter, 3rd Medical School, Charles University and University Hospital Kralovske Vinohrady
    Prague, 10034, Czech Republic
    Recruiting
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References and documents

Publications

  • Zoni-Berisso M, Filippi A, Landolina M, Brignoli O, D'Ambrosio G, Maglia G, Grimaldi M, Ermini G. Frequency, patient characteristics, treatment strategies, and resource usage of atrial fibrillation (from the Italian Survey of Atrial Fibrillation Management [ISAF] study). Am J Cardiol. 2013 Mar 1;111(5):705-11. doi: 10.1016/j.amjcard.2012.11.026. Epub 2012 Dec 28. PubMed 23273528 ↗
  • Wolf PA, Benjamin EJ, Belanger AJ, Kannel WB, Levy D, D'Agostino RB. Secular trends in the prevalence of atrial fibrillation: The Framingham Study. Am Heart J. 1996 Apr;131(4):790-5. doi: 10.1016/s0002-8703(96)90288-4. No abstract available. PubMed 8721656 ↗
  • Reddy VY, Dukkipati SR, Neuzil P, Anic A, Petru J, Funasako M, Cochet H, Minami K, Breskovic T, Sikiric I, Sediva L, Chovanec M, Koruth J, Jais P. Pulsed Field Ablation of Paroxysmal Atrial Fibrillation: 1-Year Outcomes of IMPULSE, PEFCAT, and PEFCAT II. JACC Clin Electrophysiol. 2021 May;7(5):614-627. doi: 10.1016/j.jacep.2021.02.014. Epub 2021 Apr 28. PubMed 33933412 ↗
  • Ekanem E, Reddy VY, Schmidt B, Reichlin T, Neven K, Metzner A, Hansen J, Blaauw Y, Maury P, Arentz T, Sommer P, Anic A, Anselme F, Boveda S, Deneke T, Willems S, van der Voort P, Tilz R, Funasako M, Scherr D, Wakili R, Steven D, Kautzner J, Vijgen J, Jais P, Petru J, Chun J, Roten L, Futing A, Rillig A, Mulder BA, Johannessen A, Rollin A, Lehrmann H, Sohns C, Jurisic Z, Savoure A, Combes S, Nentwich K, Gunawardene M, Ouss A, Kirstein B, Manninger M, Bohnen JE, Sultan A, Peichl P, Koopman P, Derval N, Turagam MK, Neuzil P; MANIFEST-PF Cooperative. Multi-national survey on the methods, efficacy, and safety on the post-approval clinical use of pulsed field ablation (MANIFEST-PF). Europace. 2022 Sep 1;24(8):1256-1266. doi: 10.1093/europace/euac050. Erratum In: Europace. 2023 Feb 16;25(2):449. doi: 10.1093/europace/euac250. PubMed 35647644 ↗

Individual participant data

Plan to share: No — Data will be shared 6 months after publication on request.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 19, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06198933
Responsible party
Sponsor
First posted
Jan 10, 2024
Start date
May 1, 2024
Primary completion
Dec 30, 2024 (estimated)
Completion
Dec 30, 2024 (estimated)
Last update
Sep 19, 2024

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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