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RecruitingNCT06945887TAE-DESMOUpdated Sep 12, 2025

Treatment of Desmoid Fibromatosis With Arterial Embolization

An observational study in Desmoid Fibromatosis, sponsored by Istituto Ortopedico Rizzoli. Recruiting at 1 site in Italy. Open to participants aged 12 Years and older. Per ClinicalTrials.gov, last updated 2025-09-12.

Sponsored by Istituto Ortopedico Rizzoli · Observational

From the registry’s dates

  • Started Jul 2025; still recruiting 1 year 3 months later.
Study type
Observational
Model
Cohort
Time perspective
Other
Enrollment
20
Ages
12 Years and older
Sex
All
01

Study summary

Desmoid fibromatoses are rare and locally aggressive mesenchymal tumors. The current scientific evidence regarding the efficacy and safety of the treatment of desmoid fibromatosis by arterial embolization is constituted by several retrospective and prospective studies. These studies report promising results through the use of chemoembolization, that is, arterial embolization using particles loaded with chemotherapy.

Instead, the type of treatment we propose would consist of injection of embolizing material without the use of chemotherapy, based on the positive results we have consistently reported over the years on arterial embolization of musculoskeletal tumors.

Read the detailed description

Desmoid fibromatoses are rare (1-2 cases/million per year) and locally aggressive, characterized histologically by monoclonal myoblasts present in abundant stromal tissue.The current therapeutic strategy has abandoned primary resection, as recurrences after resection are common and often their phenotype is more infiltrative. Nonsurgical approaches remain suboptimal. For asymptomatic disease, current guidelines suggest an initial period of active surveillance. The current scientific evidence regarding the efficacy and safety of the treatment of desmoid fibromatosis by arterial embolization is constituted by several retrospective and prospective studies. These studies report promising results through the use of chemoembolization, that is, arterial embolization using particles loaded with chemotherapy.

Instead, the type of treatment we propose would consist of injection of embolizing material without the use of chemotherapy, based on the positive results we have consistently reported over the years on arterial embolization of musculoskeletal tumors.

Doxorubicin is routinely used in the treatment of soft tissue sarcomas and other mesenchymal malignancies. Its use against desmoid fibromatosis is effective but associated with hematologic, gastrointestinal, and cardiac toxicity. Consequently, this drug is reserved for symptomatic, nonresponsive, rapidly growing, or life-threatening fibromatoses.

02

Conditions studied

  • Desmoid Fibromatosis

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Keywords

  • Desmoid fibromatosis
  • Embolization
03

In context

Desmoid Tumors

33 studies on the registry are indexed under Desmoid Tumors; 17 are open to participants now.

This study's planned enrollment of 20 is below the median of 100 across 10 observational studies indexed under Desmoid Tumors.

Browse Desmoid Tumors studies →

Lead sponsor

Istituto Ortopedico Rizzoli is the lead sponsor of 298 studies on the registry; 102 are open to participants now.

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

04

Who can participate

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

Study population

Patients affected by desmoid fibromatoses eligible to be treated with transarterial embolization

Inclusion criteria

  • Patients of both sexes aged ≥ 12 years
  • Fibromatosis demsoid symptomatic and in active phase (documented growth at last follow-ups)
  • Patients not eligible for surgery or cryoablation
  • Patients who have had embolization surgery for fibromatosis desmoide from 01/01/2023 to date and all new patients listed for this type of treatment.
  • Signature of informed consent to the study

Exclusion criteria

Exclusion Criteria:

  • Patients with life expectancy \<3 months or severely impaired status functional status (ASA 4)
  • Patients with fibromatosis not in active phase, documented clinically and by investigations imaging (MRI, CT)
  • Patients with coagulation deficiency or plateletopenic disease
  • Patients with documented active infection
  • Incompatibility to performing MRI examination.
05

Study design

Observational model
Cohort
Time perspective
Other
Enrollment
20 participants (estimated)
Patient registry
No

Groups and cohorts

  • Performed embolization

    Procedure: embolization therapy

Interventions

  • Procedureembolization therapy

    Identification of the main vessels afferent to the tumor to be treated. -Selective and super-selective catheterization of pathological arterial branches, responsible for the blood supply to the neoplasm, through the use of micro-catheters. - Injection of embolizing material (hydrogel microspheres) - Control of technical success: the embolization will be followed by diagnostic arteriography that will evaluate the success of the procedure (occlusion of more than 90 percent of the pathologic vasculature).

06

What researchers measure

Primary 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. Reduction of antalgic therapy (mg)

    Mean reduction in the use of pain medications evaluated in mg of active ingredient taken daily before the treatment and at follow-up.

    Time frame: 1 year

  3. Volume reduction in cm³

    Reduction of the lesion evaluated with MRI, measuring the diameter of the lesion in cm³.

    Time frame: 1 year

Secondary outcomes

  1. Improvement in quality of life (EORTC QLQ-C15-PAL questionnaire)

    Clinical assessment regarding quality of life by EORTC QLQ-C15-PAL questionnaire. The questionnaire consists of several scales, covering different aspects related to palliation. The maximum and minimum scores for each scale of the questionnaire can range from 0 to 100. The interpretation of scores depends on the specific scale in the questionnaire, and a higher value may indicate either greater negative impact (e.g., more symptoms or more suffering) or greater positive impact (e.g., better quality of life or less symptomatology).

    Time frame: 1 year

  2. Improvement in quality of life (EORTC QLQ - BM22)

    Clinical assessment regarding quality of life by EORTC QLQ - BM22 questionnaire. The questionnaire consists of several scales, covering different aspects related to palliation. The maximum and minimum scores for each scale of the questionnaire can range from 0 to 100. The interpretation of scores depends on the specific scale in the questionnaire, and a higher value may indicate either greater negative impact (e.g., more symptoms or more suffering) or greater positive impact (e.g., better quality of life or less symptomatology). The overall assessment requires a detailed analysis of individual scores and related scales.

    Time frame: 1 year

07

Study locations

1 of 1 sites recruiting
  • Istituto Ortopedico Rizzoli
    Bologna, BO 40136, Italy
    • Giancarlo Facchini, Medicine and Surgery · Contact · giancarlo.facchini@ior.it · +39 0516366836
    • Giancarlo Facchini, Medicine and Surgery · Principal investigator
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 12, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06945887
Lead sponsor
Istituto Ortopedico Rizzoli
Responsible party
Sponsor
First posted
Apr 27, 2025
Start date
Jul 1, 2025
Primary completion
Feb 2028 (estimated)
Completion
Feb 2029 (estimated)
Last update
Sep 12, 2025

Study contacts

Giancarlo Facchini, Medicine and Surgery
Contact
giancarlo.facchini@ior.it
+39 0516366836

Oversight

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

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