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NCT05113420 Clinical Trial

The Efficacy and Safety of Different Phlebotonic Drugs in Children With Venous Malformations

Surgery Clinical Trial

Official title:
The Efficacy and Safety of Different Phlebotonic Drugs in Children With Venous Malformations: a Prospective Cohort Study

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05113420
Other study ID # VAC_VM
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 17, 2019
Est. completion date September 17, 2022

Study information
Verified date October 2021
Source Center for Vascular Pathology, Moscow
Contact Ekaterina Listovskaia
Phone +79032069027
Email listovskaya_ek@outlook.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to evaluate the efficacy and safety of different phlebotonic drugs in children and to assess patient satisfaction after treatment.

Recruitment information / eligibility
Status Recruiting
Enrollment 1000
Est. completion date September 17, 2022
Est. primary completion date November 17, 2021
Accepts healthy volunteers
Gender All
Age group 1 Year to 18 Years
Eligibility Inclusion Criteria: venous malformation - venous malformation Exclusion Criteria: - allergy

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Detralex
Diosmin+ Hesperidin
• Troxevasin
Troxerutin

Locations
Country Name City State
Russian Federation The Vascular Anomalies Center (VAC) "Hemangioma" LLC Moscow

Sponsors (1)
Lead Sponsor Collaborator
Center for Vascular Pathology, Moscow

Country where clinical trial is conducted

Russian Federation, 

Outcome
Type Measure Description Time frame Safety issue
Other Satisfaction after treatment Questionnaire 1 month
Primary Coagulation testing Coagulation testing 1 month
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