MedPath

Sclerotherapy of liver hemangioma

Phase 1
Conditions
iver symptomatic hemangioma.
Haemangioma, any site
Registration Number
IRCT2016021626599N1
Lead Sponsor
Vice Chancellor for Research, Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
5
Inclusion Criteria

Patients with symptomatic liver hemangioma with therapeutic indication with confirmed diagnosis based on triphasic CT-scan or dynamic MRI.
Exclusion criteria: Those patients that their abdominal complaints could be attributed to another cause, apart from liver hemangioma

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Volume of lesion. Timepoint: 6 month after therapy. Method of measurement: Digital volumetry.
Secondary Outcome Measures
NameTimeMethod
Abdominal pain. Timepoint: one month and 6 month after procedure. Method of measurement: visual analog scale.
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