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NCT06403527Terminated

Ultrasound Guyded Venous Puncture for Safe AF Ablation Procedures

Source: ClinicalTrials.gov · Last updated 9 Feb 2026

Reason given: DSMB recommendation

Brief summary (registry, in English)

To assess if ultrasound guided venous puncture reduces the risk for access site complication in the contex of atrial fibrillation ablation.

Status (registry)
Terminated
Study type
Interventional
Enrollment
1075 (actual)
First submitted
3 May 2024
Start date
3 Mar 2024
Primary completion date
4 Feb 2026
Lead sponsor
Cardioangiologisches Centrum Bethanien
NCT number
NCT06403527

Who cannot take part

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

Other illness

  • Known coagulation disorder or Thrombocytopenia <150.000/ul.

Other

  • Patient is unable or unwilling to provide informed consent
  • Planned/required arterial access (e.g. for blood pressure monitoring)
  • Patient has contra-indication to oral anticoagulation
  • Women currently pregnant or breastfeeding or women of childbearing potential without highly effective contraception (PEARL-Index < 1%), 7. Patient is included in another clinical trial 8. Inability to comply with the study procedures

Who the study is looking for

  • Inclusion Criteria
    • Age ≥18 years
    • Signed written informed consent
    • Planned transvenous catheter ablation procedure for AF or left atrial tachycardia
    • Willingness to participate in follow-up

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. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Boris SchmidtFrankfurt am MainGermanyUnknown status

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Related publications

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