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NCT07159685Not yet recruiting

Sex-Based Differences of LA: Impact on AF Ablation.

Sex-Based Differences of Left Atrium: Impact on Atrial Fibrillation Ablation.

Source: ClinicalTrials.gov · Last updated 8 Sept 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The aim of the study is to assess sex-related differences in patients who underwent a first ablation procedure for paroxysmal or persistent AF, guided by the personalized ablation strategy of the BY-LAWT protocol. Specifically, to compare anatomical characteristics, procedural parameters, and clinical outcomes between sexes.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
700 (estimated)
First submitted
13 Aug 2025
Start date
1 Jan 2026
Primary completion date
30 Apr 2026
Lead sponsor
Centro Medico Teknon
NCT number
NCT07159685

What you commit to

  • Study type: Observational
  • Planned participants: 700
  • From 1 Jan 2026 to the primary completion date, 30 Apr 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous cardiac ablation (including AF ablation or other arrhythmias).

Other illness

  • Poor quality pre-procedural cardiac MDCT
  • Structural heart disease (e.g., dilated cardiomyopathy, valvular heart disease with surgical indication) that could substantially influence atrial dimensions or ablation response.

Age

  • Age \< 18 years.

Other

  • Incomplete data regarding procedural parameters, or follow-up.
  • Ablation not performed according to the BY-LAWT protocol.

Who the study is looking for

  • Patients who underwent a first ablation procedure for atrial fibrillation (paroxysmal or persistent).
  • Availability of an adequate pre-procedural cardiac CT scan for LAWT, LAV and inFAT analysis.
  • Availability of complete procedural data, including ablation index (AI) values recorded using the SmartTouch catheter (Biosense Webster).
  • Availability of 12-month follow-up data for efficacy and safety endpoint evaluation.
  • Ablation performed according to the by-LAWT protocol

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Teknon Medical center
Coordinator of this site? Confirm its status
BarcelonaSpainUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.