Trials / Completed
CompletedNCT06763978
Comparative Analysis of Isolated Venous, Isolated Arterial, and Standard Access for Transcatheter Closure of Patent Ductus Arteriosus (PDA)
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 357 (actual)
- Sponsor
- Egyptian Biomedical Research Network · Network
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
We enrolled all patients with a hemodynamically significant PDA demonstrated by patient clinical condition, and by PDA size \& left chamber dilatation on echocardiography attending at Cardiology Department to we compare the use of a single venous access and a single arterial access with the standard approach requiring both venous and arterial access for transcatheter PDA closure regarding the outcome \& complications.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Transcatheter PDA closure | Transcatheter PDA closure |
Timeline
- Start date
- 2020-01-01
- Primary completion
- 2024-01-31
- Completion
- 2024-01-31
- First posted
- 2025-01-08
- Last updated
- 2025-01-08
Locations
1 site across 1 country: Egypt
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT06763978. Inclusion in this directory is not an endorsement.