← Eichor
Study identifier: NCT05610501 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Ultrasound-guided Tru-Cut Biopsy in Pelvic Masses.

Condition: Pelvic Cancer · Ovarian Cancer · Cervical Cancer  ·  Sponsor: Universitaire Ziekenhuizen KU Leuven

PhaseN/A
Planned participants200
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

In a transvaginal tru-cut biopsy, guided by ultrasound, a needle is inserted through the vaginal wall into a pelvic lesion and a few pieces of tissue are obtained for examination. This clinical trial is organized to evaluate the safety and efficacy of transvaginal tru-cut biopsy in a large group of patients with tumors in the small pelvis.

This description comes directly from the study's public registry record.

Talk to the study team

Wouter Froyman, MD, PHD  ·  +3216344202  ·  wouter.froyman@uzleuven.be

Stefan Timmerman, MD  ·  stefan.timmerman@uzleuven.be

Always discuss trial participation with your own doctor first.

Locations (4)

UZ LeuvenLeuven, BelgiumRecruiting
First Faculty of Medicine, Charles UniversityPrague, CzechiaNot Yet Recruiting
Fondazione Policlinico Universitario A. Gemelli, IRCSSRome, ItalyNot Yet Recruiting
Department of Clinical Science and Education, Karolinska Institutet and Department of Obstetrics and Gynecology, SödersjukhusetStockholm, SwedenNot Yet Recruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT05610501