Multi-institutional clinical study to verify the efficacy and safety of wearing custom-made compression elastic garment in cases of Klippel-Trenaunay syndrome

Multi-institutional clinical study to verify the efficacy and safety of wearing custom-made compression elastic garment in cases of Klippel-Trenaunay syndrome - Custom-made compression elastic garment in Klippel-Trenaunay syndrome

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000038282

Enrollment

Registered

2019-10-12

Start date

2019-10-15

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Vascular malformation Klippel-Trenaunay syndrome

Interventions

Wearing custom-made garments

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients as Klippel-Trenaunay syndrome Over 2 years of age Patients having the lesion on the calf Patients who can walk independently

Exclusion criteria

Exclusion criteria: Patients who received surgical interventions including sclerotherapy within 12 weeks Patients who have allergy against the garment materials Patients who must keep taking diuretic agents Patients who suffered from heart failure within one year

Design outcomes

Primary

Measure	Time frame
Lower limb circumferences on the affected side	—

Countries

Japan

Contacts

Public ContactShunsuke Yuzuriha

Shinshu University School of Medicine Department of Plastic and Reconstructive Surgery

yuzuriha@shinshu-u.ac.jp0263-37-2833

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026