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Precision Interventional embolization for Pediatric Peripheral Arteriovenous Malformations Using Medical-Engineering Technology

Precision Interventional embolization for Pediatric Peripheral Arteriovenous Malformations Using Medical-Engineering Technology

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123636
Enrollment
Unknown
Registered
2026-04-28
Start date
2026-04-28
Completion date
Unknown
Last updated
2026-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pediatric peripheral arteriovenous malformations (AVMs)

Interventions

Navigation Group:Intraoperative 3D fusion navigation
Past interventional therapy group:Routine embolization therapy

Sponsors

Beijing Childrens Hospital,Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: 1. Age 0-18 years old, both sexes; 2.Diagnosed with peripheral arteriovenous malformations involving the extremities or trunk by ultrasonography and computed tomography angiography (CTA); 3.Candidates for interventional embolization treatment; 4.Informed consent has been signed by the legal guardian, and the patient is able to comply with the follow-up schedule;

Exclusion criteria

Exclusion criteria: 1.Severe cardiac, hepatic, or renal insufficiency, or coagulation dysfunction; 2.The lesion involves central blood vessels or visceral blood vessels; 3.Hypersensitivity to contrast agents or embolic materials; 4.Unable to comply with postoperative follow-up;

Design outcomes

Primary

MeasureTime frame
First-pass superselective success rate: the percentage of cases in which the microcatheter is successfully placed into the target feeding artery in one attempt.;Occlusion rate of malformation at 6 months after operation: the proportion of complete occlusion of malformation detected by ultrasound/CTA;

Secondary

MeasureTime frame
Operation time (from puncture to dressing completion);Radiation dose (dose area product DAP);Dosage of contrast medium;Symptom improvement score (pain, disability);

Countries

China

Contacts

Public ContactCheng Wei

Beijing Childrens Hospital,Capital Medical University

drchengwei@126.com+86 10 59616786

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026