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NCT04627948Completed

STHLM3 AS NorDCaP - a Followup Study of Men on Active Surveillance of Prostate Cancer

Source: ClinicalTrials.gov · Last updated 21 Jan 2025

Brief summary (registry, in English)

The aim of the STHLM3 AS NorDCaP study is to evaluate the Stockholm3 test in an active surveillance cohort to predict upgrading on rebiopsy. The study follows a paired design, evaluating our proposed protocol for follow up men on active surveillance with Stockholm3 versus the standard protocol according to national guidelines with PSA.

Status (registry)
Completed
Study type
Observational
Enrollment
199 (actual)
First submitted
5 Nov 2020
Start date
1 Jul 2019
Primary completion date
1 Jul 2024
Lead sponsor
Karolinska Institutet
NCT number
NCT04627948

What you commit to

  • Study type: Observational
  • Participants enrolled: 199
  • From 1 Jul 2019 to the primary completion date, 1 Jul 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • History of treatment for prostate cancer; surgery, radiation, chemotherapy or hormonal treatment.
  • Severe illnesses such as metastatic cancers, severe cardio-vascular disease or dementia

Who the study is looking for

  • Men diagnosed with low-risk PC and currently on AS and planned for follow-up with systematic and/or fusion biopsies as following standard of care.

Age in the registry: 40 years to 75 years · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Karolinska Institutet
Coordinator of this site? Confirm its status
StockholmSwedenUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.