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RecruitingNCT07579962BESTUpdated Oct 9, 2026

Treatment of Low-flow Vascular Malformations With Bleomycin Electrosclerotherapy (BEST)

A Phase 2 interventional study of Bleomycin Sulfate in Vascular Malformations, sponsored by Institute of Oncology Ljubljana. Recruiting at 1 site in Slovenia. Open to participants aged 18 Years to 99 Years. Per ClinicalTrials.gov, last updated 2026-10-09.

Sponsored by Institute of Oncology Ljubljana · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Started Sep 2026; still recruiting 2 months later.
Updated Oct 9, 2026Now RecruitingFirst site in Slovenia+2 moreGo to Updates ↓
Phase
Phase 2
Study type
Interventional
Enrollment
140
Allocation
Not applicable
Ages
18 Years to 99 Years
Sex
All
01

Study summary

In biomedical applications, electroporation is used not only for cancer treatment but also for vaccinations, treatment of cardiac arrhythmias and, more recently, for the treatment of vascular malformations. Bleomycin is a frequently used sclerosing agent in the treatment of various vascular malformations. The use of electrical pulses in addition to bleomycin increases the effectiveness of the treatment, similar to electrochemotherapy. Bleomycin electrosclerotherapy (BEST) is a new treatment modality that is effective in the treatment of low-flow malformations (venous and lymphatic malformations) and potentially also high-flow malformations (arteriovenous malformations). Although a limited number of reports have been published to date, more and more centers are using BEST for the treatment of vascular malformations. As part of the International Network for Sharing Practices on Electrochemotherapy (InspECT) consortium, a dedicated working group has been set up to develop standard operating procedures for BEST. Current Operating Procedures have been prepared and will be used in this clinical trial.

Read the detailed description

Vascular malformations are rare conditions caused by abnormally developed blood vessels. They can occur anywhere in the body and range from simple and benign lesions to complex conditions.

The latest and most commonly used categorization is the International Society for the Study of Vascular Anomalies (ISSVA) classification. This classification divides vascular anomalies into two main categories: tumors, defined as true proliferative neoplasms, and malformations, defined as morphogenetic defects. These two categories are further subcategorized: tumors are divided into benign, locally aggressive/borderline, and malignant tumors, whereas malformations are subdivided into simple, combined, or associated with other anomalies. Clinically, vascular anomalies can also be divided into low-flow and high-flow malformations.

Current treatment of vascular malformations varies depending on the type and anatomical location of the vascular malformation. Treatment options include observation, sclerotherapy, laser therapy, embolization, and surgery. Sclerotherapy involves the injection of sclerosing agents, such as bleomycin, pingyangmycin, absolute ethanol, ethanolamine oleate, polidocanol, doxycycline, cyanoacrylate, sodium morrhuate, and sodium tetradecyl sulfate (STS).

Current treatment options for low-flow vascular malformations remain suboptimal. Current therapies demonstrate limited clinical efficacy. Ethanol is widely used as a sclerosing agent and can induce substantial lesion regression; however, its clinical utility is limited by considerable safety concerns. In particular, ethanol may induce extensive tissue necrosis and damage to surrounding healthy structures, which limits its therapeutic use.

Another agent frequently employed for sclerotherapy is bleomycin. However, when administered as monotherapy, without the use of electroporation, bleomycin often shows insufficient therapeutic effectiveness. In many cases, treatment results only in minor reduction of lesion volume and fails to adequately alleviate patient-reported symptoms, including pain and functional discomfort.

Electrochemotherapy is a local ablative treatment in which electroporation is used to enhance the delivery of cytotoxic molecules, such as bleomycin or cisplatin, to treat cancer. The cytotoxicity of the drug is increased only at the site of electrical pulse application. This approach is often used to treat both skin tumors and deep-seated tumors, such as liver and pancreatic tumors. Several types of electrodes have been designed to optimize the delivery of electrical pulses to specific anatomical sites. The efficacy of electrochemotherapy ranges from 70% to 80%. Electrochemotherapy is included in many national and international guidelines as a local ablative therapy and is practiced in more than 200 centers throughout Europe.

There are three underlying mechanisms of electrochemotherapy. The first is enhanced drug delivery to tumor cells, which die due to the cytotoxicity of the drugs, either by apoptosis or necrosis. This is predominantly related to the drug used and its mode of action. Bleomycin, for example, induces mitotic cell death, which leads to slow resolution of the tumor mass.

The second mechanism is the induction of an immune response due to immunogenic tumor cell death induced by the drug. It is well established that certain ablative therapies induce immunogenic cell death that can attract and enhance the immune response of the organism.

The third mechanism is the vascular disrupting effect of electrochemotherapy. In early preclinical research, it was established that the application of electrical pulses only temporarily abrogates blood flow within tumors. This phenomenon was termed vascular lock and lasts less than an hour. Furthermore, the effect is enhanced when the drug is present during the application of electrical pulses. Investigations have shown that this results in vascular disruption that occurs within hours in tumors. Endothelial cells start to die, blood flow is obstructed, and secondary tumor cell death is induced within days due to tumor hypoxia.

The phenomenon is predominantly confined to the tumor vasculature, sparing the normal vasculature around the tumors. This is because of the high proliferation rate of endothelial cells in tumors compared with the vasculature in normal tissues, where the endothelial proliferation rate is very slow. The vascular disrupting effect of electrochemotherapy is not fully understood. To date, the proportion by which this vascular disrupting effect contributes to the overall effectiveness of electrochemotherapy in specific tumor types is not fully understood. The effect appears to depend on the distribution and extent of tumor vascularization, with better vascularized tumors generally responding better to electrochemotherapy.

02

Conditions studied

  • Vascular Malformations

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Keywords

  • vascular malformations
  • electroporation
  • bleomycin
  • electrosclerotherapy
  • low flow vascular malformations
03

In context

Vascular Malformations

79 studies on the registry are indexed under Vascular Malformations; 33 are open to participants now.

This study's planned enrollment of 140 is above the median of 55 across 49 interventional studies indexed under Vascular Malformations.

Browse Vascular Malformations studies →

Lead sponsor

Institute of Oncology Ljubljana is the lead sponsor of 81 studies on the registry; 26 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 99 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • age ≥ 18
  • patients with low-flow vascular malformations (venous, lymphatic, capillary or mixed type malformations),
  • patients with a low-flow vascular malformation poorly responding or recurring after previous treatment(s),
  • longer lesion diameter not exceeding 25 cm.
  • more than one lesion can be treated. The limiting factor is the maximal dose per patient per treatment session; 10 000 IU in adults,
  • skin or mucosal, superficial or deep-seated lesions can be treated,
  • technical feasibility of the BEST procedure, i.e.: injection of bleomycin and safe placement of electrodes into the vascular malformation are technically feasible.

Exclusion criteria

Exclusion Criteria:

  • pregnancy and lactation,
  • women of and men not using reliable ,
  • in adults, previous bleomycin exposure with a cumulative dose greater than 100 000 IU. In case of abnormal respiratory results/chest pathology (including previous severe or long COVID) in consultation with a pulmonologist, special care is required, and bleomycin exposure may be ,
  • known allergy or to bleomycin,
  • presence of significant central venous drainage precluding sclerotherapy,
  • acute lung infection or severely reduced lung function,
  • bleomycin-related lung toxicity or reduced lung function which can indicate bleomycin-related lung toxicity,
  • ataxia telangiectasia,
  • chronic renal dysfunction.
Terms in these criteria, in plain language(4)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
140 participants (estimated)

Study arms

  • Experimental
    Bleomycin electrosclerotherapy

    Participants with low-flow vascular malformations will receive intralesional bleomycin combined with local application of electrical pulses according to the BEST procedure.

    Drug: Bleomycin Sulfate

Interventions

  • Bleomycin will be administered by local intralesional injection into the vascular malformation, followed by application of electrical pulses.

    Also known as: Bleomycin Electrosclerotherapy

06

What researchers measure

Primary outcomes

  1. MRI-measured mean change in lesion volume from baseline to 3 months after BEST treatment

    Lesion volume will be assessed by magnetic resonance imaging at baseline and 3 months after treatment. Lesion volume will be calculated from MRI images using the ellipsoid formula: a x b x c x π/6. The outcome measure will report the mean change in lesion volume from baseline to 3 months after BEST treatment.

    Time frame: Baseline and 3 months after treatment

Secondary outcomes

  1. MRI-measured mean change in lesion volume from baseline to 12 months after BEST treatment

    Lesion volume will be assessed by magnetic resonance imaging at baseline and 12 months after treatment. Lesion volume will be calculated from MRI images using the ellipsoid formula: a x b x c x π/6. The outcome measure will report the mean change in lesion volume from baseline to 12 months after BEST treatment.

    Time frame: Baseline and 12 months after treatment

  2. Number of participants who complete protocol-defined BEST treatment and follow-up visits

    Feasibility will be assessed by the number of participants who complete the protocol-defined BEST treatment and scheduled follow-up visits at 3 months and 12 months after treatment.

    Time frame: Up to 12 months after treatment

  3. Number of participants with treatment-emergent adverse events as assessed by CTCAE version 5.0

    Treatment-emergent adverse events will be recorded, classified according to MedDRA terminology, graded using CTCAE version 5.0, and assessed for relationship to the investigational medicinal product or procedure.

    Time frame: Up to 12 months after treatment

  4. Change in quality of life from baseline to 3 and 12 months after BEST treatment as assessed by the OVAMA questionnaire

    Quality of life will be assessed using the OVAMA questionnaire at baseline, 3 months, and 12 months after treatment. The outcome measure will report the change in OVAMA questionnaire results from baseline to 3 and 12 months after BEST treatment.

    Time frame: Baseline, 3 months, and 12 months after treatment

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Status
Not yet recruiting→Recruiting
changed Oct 9, 2026
Sites
1 site added — first site in Slovenia
Show site
  • Institute of Oncology Ljubljana · Ljubljana, Slovenia
Oct 9, 2026
Start date
Jun 30, 2026→Sep 10, 2026 (actual)
Oct 9, 2026
Show all 1 update
  1. Oct 9, 2026
    Not yet recruiting→Recruiting
    1 site added — first site in Slovenia
    Show site
    • Institute of Oncology Ljubljana · Ljubljana, Slovenia
    Start date Jun 30, 2026→Sep 10, 2026 (now actual)
    + 2 other changes: identifiers and verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07579962
Lead sponsor
Institute of Oncology Ljubljana
Responsible party
Sponsor
First posted
May 12, 2026
Start date
Sep 10, 2026
Primary completion
Jun 30, 2031 (estimated)
Completion
Jun 30, 2032 (estimated)
Last update
Oct 9, 2026

Study contacts

Neža Gros
Contact
ngros@onko-i.si
031860131
Gregor Serša
study chair · Institute of Oncology Ljubljana

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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Studies of the drug tested here: Bleomycin

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