RecruitingNot applicableMale onlyEN originalProstate cancer

SPECTRA: Intraoperative Hyperspectral Imaging for Prostate Cancer

⚠️

This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.

About the trial

Radical prostatectomy (RP) is currently one of the gold standard of care in managing localized prostate cancer (Pca). However, despite advances in Robot-Assisted RP (RARP), cancer cells may still be found (up to 42%) at the edge of the removed prostate specimen, commonly referred as Positive Surgical Margins (PSM). PSM are well-known risk factors of adverse oncological outcomes (biochemical recurrence). It is therefore essential to characterize intraoperatively the tumor extent. In RARP, the leading intraoperative margin assessment (IMA) technique, NeuroSAFE is based on Intra-operative frozen section (IFS) of both prostate lateral sides sampled at 3-5 mm intervals. However, despite proven oncological benefit, adoption is still limited to expert centers due to a prolonged operative time, loss of integrity of the surgical specimen for definitive histopathological analysis, omission of regions (apex, base), and logistical complexity (trained uropathologist, cryostat…). With this prospective single-center project, we wish to explore the use of non-invasive optical imaging technology, HyperSpectral Imaging (HSI), as a reliable alternative for examination of the ex-vivo prostate specimen to 1. Distinguish normal versus tumor tissue at the surgical margin in fresh specimen. 2. Quantify whether HSI can be integrated into the intraoperative workflow (feasibility), thus, image acquisition time and inference time should then be evaluated.

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • •Potwierdzony biopsją rak prostaty
  • •Prostata o objętości poniżej 100 cm³ (zmierzona przed operacją)
  • •Zdolność do samostanowienia i wyrażenia zgody na uczestnictwo

✗ Disqualifies

  • •Brak chęci do udziału w badaniu
  • •Niemożność przestrzegania procedur badania (problemy z językiem, zaburzenia psychiczne, demencja)

Simplified criteria — AI translation

Trial details

Minimum age
18 Years
Last updated (source)
September 17, 2026
Sex
Male only

Therapies / drugs in trial

Locations (1)

Hôpitaux Universitaires de Genève - Dept de Chirurgie - Service d'Urologie

Geneva, Switzerland

Trial contact

Contact information from ClinicalTrials.gov. Contact in English.

Share this trial

Data from ClinicalTrials.gov. AI-assisted translation, last sync: 9/18/2026.

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