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Effectiveness of Sirolimus in Treating Vascular and Lymphatic Malformations in Thai Pediatric Patients

Ambidirectional Observational Study of Sirolimus for Vascular and Lymphatic Malformations in Thai Pediatric Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20260618002
Enrollment
30
Registered
2026-06-18
Start date
2025-09-02
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

Vascular malformations Lymphatic malformations Venous malformations Klippel-Trenaunay syndrome Veno-lymphatic malformations Arteriovenous malformations Sirolimus Vascular Malformations Lymphatic Malformations Venous Malformations Pediatrics Quality of Life

Interventions

Pediatric patients aged 1 day to 18 years with vascular and lymphatic malformations who received sirolimus treatment at King Chulalongkorn Memorial Hospital. Patients were enrolled in an ambidirection
Treatment
Pediatric Vascular and Lymphatic Malformations

Sponsors

Kuakul Kiatphirakul, MD
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Days to 18 Years

Inclusion criteria

Inclusion criteria: 1 Pediatric patients aged 1 day to 18 years who were treated at the inpatient and/or outpatient departments of King Chulalongkorn Memorial Hospital 2 Diagnosed with vascular and/or lymphatic malformations 3 Received sirolimus treatment for vascular and/or lymphatic malformations 4 Patients treated during the 10 year retrospective period prior to IRB approval and newly diagnosed patients enrolled prospectively following IRB approval during the study period

Exclusion criteria

Exclusion criteria: 1 Patients whose diagnosis of vascular and/or lymphatic malformations was subsequently revised to another diagnosis 2 Patients with incomplete clinical data

Design outcomes

Primary

MeasureTime frame
Clinical response rate 6 months Proportion of patients achieving complete response or partial response based on clinical assessment

Secondary

MeasureTime frame
Adverse events 12 months Incidence and types of adverse events during sirolimus treatment,Quality of life 6 months Change in quality of life scores using InToDermQoL and CDLQI

Countries

Thailand

Contacts

Public ContactKuakul kiatphirakul

Department of Pediatrics Faculty of Medicine Chulalongkorn University

kuakulkiat@gmail.com022564951

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026