RecruitingNCT05264753
Post Marketing Clinical Follow Up Study to Evaluate Efficacy and Safety of the Occlutech PDA Occluder in Patients With Patent Ductus Arteriosus Defects
Studying Arterial duct anomaly
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Occlutech International AB
- Intervention
- Occlutech® PDA Occluder(device)
- Enrollment
- 255 enrolled
- Eligibility
- All sexes
- Timeline
- 2021 – 2029
Study locations (15)
- CHU Sainte-Justine, Montreal, Canada
- CHU de Lille - Institut Cœur-Poumon, Lille, France
- Hôpital Mère Enfant, CHU de Nantes, Nantes, France
- Children's Hospital Ireland at Crumlin, Dublin, Ireland
- Ospedale Pediatrico Bambino Gesù, Roma, Roma, Italy
- Rawalpindi Institute of Cardiology, Rawalpindi, Rawalpindi, Pakistan
- Children´s Hospital, Karolinska University, Stockholm, Sweden
- Insel Gruppe, Bern, Switzerland
- Hospital La Rabta, Tunis, Tunisia
- Military Hospital, Tunis, Tunisia
- Aydın Adnan Menderes University Hospital, Aydin, Efeler, Turkey (Türkiye)
- Eskişehir Osmangazi University Hospital, Eskişehir, Eskişehir, Turkey (Türkiye)
- Çukurova University Hospital, Adana, Sarıçam, Turkey (Türkiye)
- Dicle University Hospital, Diyarbakır, SUR, Turkey (Türkiye)
- Royal Brompton & Harefield Hospitals, London, London, United Kingdom
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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