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Construction of a rare disease sample bank for Klippel-Trenaunay Syndrome(KTS)

Construction of a rare disease sample bank for Klippel-Trenaunay Syndrome(KTS)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500111533
Enrollment
Unknown
Registered
2025-11-01
Start date
2025-11-01
Completion date
Unknown
Last updated
2025-11-03

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

Conditions

Klippel-Trenaunay Syndrome

Interventions

Observation Group of Lower extremity venous Malformations and bone hypertrophy syndrome:None

Sponsors

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with Klippel-Trenaunay syndrome, regardless of age or gender. 2. Voluntarily participate in this clinical project and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Merge patients with severe primary diseases of the heart, lungs, liver, kidneys, hematopoietic system, endocrine system, or mental illnesses. 2. The patient is unwilling or unable to cooperate with treatment or follow medical advice.

Design outcomes

Primary

MeasureTime frame
Mutated gene;—

Countries

China

Contacts

Public ContactRuihua Wang

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine

112814732@qq.com+86 21 23271699

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026