Percutaneous Sclerotherapy of Symptomatic Liver Hemangioma With Bleomycin

Phase 1

Completed

• Conditions: Hemangioma Liver
• Interventions: Procedure: sclerotherapy arm

• Registration Number: NCT03649113
• Lead Sponsor: Tehran University of Medical Sciences

Brief Summary

Percutaneous sclerotherapy is currently a widely used treatment for subcutaneous low-flow vascular malformations. Considered as a low-flow vascular malformation, symptomatic liver hemangiomas could also theoretically be safely and effectively treated by percutaneous sclerotherapy with a mixture of Bleomycin and Lipiodol. The safety and efficacy of percutaneous sclerotherapy was firstly introduced by the investigator's investigators in 5 patients in a pilot study. The aim of this study is to design and conduct a study to evaluate the safety and efficacy of percutaneous sclerotherapy in a larger sample size with a long term follow-up.

Detailed Description

Twenty-five patients with symptomatic liver hemangioma will be enrolled after an informed consent being obtained. Patients' symptoms related to liver mass, including the pain severity being measured by visual analogue scale, discomfort, early satiety, or nausea will be recorded. Liver function tests, coagulation tests, and complete blood count will be checked before the intervention. A triple phase abdominal CT scan with the administration of intravenous contrast medium will also be performed before the procedure. Exclusion criteria include hepatic or renal impairment, abdominal symptoms unrelated to a liver mass, uncorrectable coagulopathy, lung fibrosis, allergy to contrast media, systemic infection, liver abscess, and biliary obstruction.

Patients will be sufficiently hydrated with normal saline before the procedure. Corticosteroid and prophylactic antibiotics will be administered before the procedure. Antibiotics will be continued for 3 days after the procedure.

The liver mass will be punctured under guidance of ultrasonography with a 20- or 22-gauge Chiba needle. Contrast medium will be injected under fluoroscopy guidance to assess any possible communication with the biliary tree and to evaluate the amount of sclerosing agent which could be safely injected. Then, the mixture of Bleomycin (Bleocin-S; Korea United Pharm Inc., South Korea) and Lipiodol (Ultra-Fluid, Guerbet, France) will be slowly injected under continuous guidance of fluoroscopy. No more than 45 units of Bleomycin and 15 cc of Lipiodol will be injected in a single session.

Any complication taking place during and within 30 days after the procedure will be recorded. Liver function tests, coagulation tests, and complete blood count will be repeated the day after the procedure, and 6 months after the procedure. Also, a triple phase abdominal CT scan will be repeated in 6 months, and 12 months after the intervention. The patients' symptoms will be asked by phone after 12 months. The changes in lesion size on CT scan and in patients' symptoms will be evaluated.

Study Timeline

• Study First Submitted: 2018-07-19
• Study First Submitted QC: 2018-08-25
• Study First Posted: 2018-08-28
• Study Start: 2018-09-01
• Primary Completion: 2019-09-01
• Status Verified: 2019-10
• Study Completion: 2020-07-01
• Last Update Submitted: 2020-10-06
• Last Update Posted: 2020-10-08

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 25

Inclusion Criteria

• patients with symptomatic liver hemangioma

Exclusion Criteria

• hepatic or renal impairment
• abdominal symptoms unrelated to a liver mass
• uncorrectable coagulopathy
• lung fibrosis
• allergy to contrast media
• systemic infection
• liver abscess
• biliary obstruction

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
sclerotherapy arm	sclerotherapy arm	Patients with symptomatic liver hemangioma undergoing sclerotherapy (percutaneous injection) with 45 units of Bleomycin once during the procedure

Primary Outcome Measures

Name	Time	Method
Change in patient satisfaction assessed by the Visual Analog Scale (VAS) after 6 months	6 months	Pain is subjectively assessed based on a visual analog scale (VAS) before and 6 months after intervention. Change in VAS is recorded.; VAS is between zero (no pain at all) and 10 (worst pain imaginable).

Secondary Outcome Measures

Name	Time	Method
Change in hemangioma size	6 months	The size of the hemangioma is assessed on CT scans performed before and 6 months after the procedure. The largest diameter of the hemangioma is measured on axial images.
Incidence of major adverse events	During the procedure and within 30 days after the procedure	Incidence of major adverse events that may cause any of the following: A) Require therapy, minor hospitalization (less than 48 hours) B) Require major therapy, unplanned increase in level of care, prolonged hospitalization (more than 48 hours) C) Permanent adverse sequel D) Death

Trial Locations

Locations (1)

Imam Khomeini Hospital Complex, Tehran University of Medical Sciences; 🇮🇷 Tehran, Iran, Islamic Republic of