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NCT03535610: EMBOSOFT I

Uterine Artery Embolization With Microspheres in Patients With Leiomyoma.

Completed NA Last updated 4 September 2020
What this trial tests

NA trial testing Uterine Embolization in Uterine Leiomyoma in 32 participants. Completed in 20 May 2020.

Timeline
13 August 2018
Primary endpoint
20 February 2020
20 May 2020

Quick facts

Lead sponsorScitech Produtos Medicos SA
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment32
Start date13 August 2018
Primary completion20 February 2020
Estimated completion20 May 2020
Sites1 location across Brazil

Drugs / interventions tested

Conditions studied

Sponsor

Scitech Produtos Medicos SA — full company profile →

Who can join

Adults 18 to 50, female only, with Uterine Leiomyoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To evaluate the therapeutic response to uterine artery embolization in 30 patients with leiomyoma using the microspheres Embosoft (Embosoft® - Scitech Medical).

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Uterine artery embolization with highly compressible calibrated microspheres for the treatment of uterine fibroids.
    Szejnfeld D, Santos RFT, Kambara AM, Colli MBO, et al · · 2022 · cited 1× · PMID 35983349 · DOI 10.1590/0100-3984.2021.0123

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Other Scitech Produtos Medicos SA trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03535610.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing