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NCT Number: NCT06634407

Outcome of Transcatheter Closure of Patent Ductus Arteriosus in Pediatric Cardiology Unit in 3 Years Duration

Transcatheter Closure of Patent Ductus Arteriosus to evaluate the outcome of percutaneous transcatheter closure of patent ductus arteriosus in children

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children with Patent Ductus Arteriosus confirmed by echocardiography
  • aged from 6 months to 16 years underwent percutaneous transcatheter PDA closure at Pediatric Cardiology Unit.

Exclusion criteria

  • Children with PDA younger than 6 months or older than 16 years and that are not candidate for transcatheter closure .

Treatment and study plan

transcatheter closure

Procedure

using transcatheter closure of PDA to detect outcome of patients with PDA

Primary outcomes

  1. outcome of trancathter PDA closure

    Time frame: 3 years

    outcome of 90 patients with trancatheter PDA closure in pediatrics using post procedure catheter and echocardiography

Study contacts

Contact information is provided by the study sponsor or research team.

Bassem Eldaba Fares bassem fares

CONTACT

[email protected]

+201220851469

Sponsors and collaborators

Lead sponsor

Assiut University

Other

Registry information

Official study title

Transcatheter Closure of Patent Ductus Arteriosus. Experience of Pediatric Cardiology Unit-Assiut University Hospital

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Oct 9, 2024
Registry last updated
Oct 22, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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