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Comparison of bleomycin versus Vascular endothelial growth factor inhibitor percutaneous injection in the treatment of extremity vascular anomaly: A randomized control trial

Comparison of bleomycin versus Vascular endothelial growth factor inhibitor percutaneous injection in the treatment of extremity vascular anomaly: A randomized control trial

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20240524002
Enrollment
48
Registered
2024-05-24
Start date
2024-04-28
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

extremity vascular anomaly hemangioma, vascular anomaly, bleomycin, VEGF inhibitor, bevacizumab

Interventions

patient will be given intralesional bevacizumab(100mg/4ml) dose 1 mg/cubic centimeter by ultrasound guide,patient will be given intralesional bleomycin(1mg/ml) dose 0.6 mg/kg by fluoroscopy guide
Experimental Drug,Active Comparator Drug
Bevacizumab,bleomycin

Sponsors

Research department, faculty of medicine siriraj hospital, mahidol univerisy
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.patient that diagnosed infiltrative lesion extremity vascular anomaly by MRI 2.tumor size > 3 cm. 3.pain score 3 points or higher from Visual analog scale (VAS) 4.age 12-80 years old 5.new case or recurrent case

Exclusion criteria

Exclusion criteria: 1. pregnant 2. allergy to contrast media 3. allergy to bleomycin or VEGF inhibitor

Design outcomes

Primary

MeasureTime frame
tumor size at 6 and 12 months after intervention MRI

Secondary

MeasureTime frame
pain score at 6 and 12 months after intervention visual analog scale

Countries

Thailand

Contacts

Public ContactChandhanarat Chandhanayingyong

Faculty of Medicine Siriraj Hospital, Mahidol University

chandhanarat@gmail.com0959109606

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026