ClinicalTrials.gg
RecruitingNCT06189092BESVAMUpdated May 22, 2026

Treatment of Low-flow Venous Malformations With Electrosclerotherapy. Prospective Observational Study

An observational study in Vascular Malformations, sponsored by Istituto Ortopedico Rizzoli. Recruiting at 1 site in Italy. Open to participants aged 16 Years and older. Per ClinicalTrials.gov, last updated 2026-05-22.

Sponsored by Istituto Ortopedico Rizzoli · Observational

From the registry’s dates

  • Started Oct 2023; still recruiting 3 years later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
65
Ages
16 Years and older
Sex
All
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Study summary

Venous malformations (MVs) are congenital abnormalities of the central or periphery caused by developmental errors at different stages of embryogenesis. Histologically they are characterized by large, venous-like vascular spaces. Scleroembolization constitutes the most widespread method in the treatment of venous malformations allowing good results with low invasiveness. Currently, Bleomycin (and its derivatives) is among the most widely used sclerosing agents for slow-flowing vascular malformations (venous and lymphatic malformations) because of the low rate of local serious adverse events such as swelling, necrosis, and nerve injury compared with others.

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Conditions studied

  • Vascular Malformations

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Keywords

  • Electrosclerotherapy
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 65 is below the median of 200 across 27 observational studies indexed under Vascular Malformations.

Browse Vascular Malformations studies →

Lead sponsor

Istituto Ortopedico Rizzoli is the lead sponsor of 304 studies on the registry; 103 are open to participants now.

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

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Who can participate

Ages eligible
16 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients affected by low-flow vascular malformations

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

  • Diagnosis of low-flow venous malformations eligible for electrosclerotherapy
  • Non-indication for embolizing treatment
  • Previous treatments are not an exclusion factor, provided that at least 30 days have elapsed.

Exclusion criteria

Exclusion Criteria:

  • Previous treatment for \< 30 days
  • Pregnancy and lactation status
  • Patients of childbearing age without use
  • Presence of metal synthetic media
  • with FiO2 \< 30 mmHg
  • Impaired renal function with \<30 ml/min/1.73mq
  • Patients with Bleomycin intolerance or previous episodes of toxicity Bleomycin-related
  • Patients who have already received a cumulative dose of Bleomycin ≥100 mg
  • Patients who have undergone prior thoracic radiotherapy
  • Patients with a history of seizures and epilepsy
Terms in these criteria, in plain language(3)

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.

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.

COPD

Chronic obstructive pulmonary disease: long-term lung disease that makes it hard to breathe out, including emphysema and chronic bronchitis.

GFR and eGFR (kidney filtering)

GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².

Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
65 participants (estimated)
Target follow-up
1 Year
Patient registry
Yes

Groups and cohorts

  • Performed electrosclerotherapy

    All patients who performed electrosclerotherapy in the treatment of vascular malformations

    Drug: Bleomycin

Interventions

  • Using electroporation to infuse bleomycin in the lesion

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What researchers measure

Primary outcomes

  1. Volume reduction in cm

    Reduction of the lesion of at least 30% evaluated with MRI, measuring the diameter of the lesion in cm.

    Time frame: 1 year

Secondary outcomes

  1. Reduction of pain (VAS score)

    Clinical assessment regarding pain by Visual Analogue Scale (VAS) score (0-100 mm), in which 0 represents no pain, and 100 represents maximum pain imaginable.

    Time frame: 1 year

  2. Improvement in quality of life ( EuroQol-5D questionnaire)

    Clinical assessment regarding quality of life by EuroQol-5D questionnaire. EQ-5D score can range from -0.594 to 1.0. The minimum value represents the worst possible health condition. The maximum value of 1.0 represents the best possible health condition. A value of 1.0 indicates that the patient has no problem in any of the five dimensions assessed by the questionnaire.

    Time frame: 1 year

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Study locations

1 of 1 sites recruiting
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06189092
Responsible party
Sponsor
First posted
Jan 3, 2024
Start date
Oct 28, 2023
Primary completion
Nov 28, 2026 (estimated)
Completion
Nov 28, 2027 (estimated)
Last update
May 22, 2026

Oversight

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

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No contact was published for this record. The registry link below has the sponsor’s details.

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