Oncolgy Network of Piemonte and Valle d'Aosta - Turin
Turin, 10126, Italy
NCT Number: NCT03348722
The purpose of the START project is to evaluate the acceptability, the safety and the cost-effectiveness of a population based program of active surveillance for patients newly diagnosed with a localized, low risk, prostate cancer.
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Notify Me18 year and older
Male
Observational
Turin, 10126, Italy
Comparative effectiveness research project. All newly diagnosed prostate cancer patients fulfilling the low risk definition, resident in Piedmont or in Valle D'Aosta regions, will be invited to participate. All enrolled patients will receive full and clear information about their prognosis together with a balanced synthesis of the benefits and risks of the available treatments (active surveillance or radical treatments).
Specific objectives are:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
IInclusion Criteria:
Exclusion criteria
PSA testing (every 3 months, then every 6 after 30 months), clinical visit and DRE every 6 months, prostate biopsy after 1, 4 and 7 years
Radical prostatectomy (open, laparoscopic or robotic)
External radical radiotherapy or brachitherapy
High intensity focal ultrasound, cryotherapy, others
Time frame: Up to 24 months
Proportion of patients in active surveillance program alive and not undergoing active treatment for prostate cancer.
Time frame: Up to 24 months
Measured through validated questionnaire EORTC QLQ-C30 at baseline and every six months during the first 2 years.
Time frame: Up to 24 months
Measured through validated questionnaire QLQ-PR25 at baseline and every six months during the first 2 years.
Time frame: Up to 24 months
Measured through validated questionnaire IPSS at baseline and every six months during the first 2 years.
Time frame: Up to 24 months
Measured through validated questionnaire IIEF-5 at baseline and every six months during the first 2 years.
Time frame: Up to 24 months
Measured through validated questionnaire HADS at baseline and every six months during the first 2 years.
Time frame: Up to 24 months
Measured through validated questionnaire EuroQol-5D at baseline and every six months during the first 2 years.
Time frame: Up to 24 months
Measured through validated questionnaire MHLC -Form C at baseline and every six months during the first 2 years.
Time frame: Up to 24 months
Incremental cost-effectiveness ratio calculated as the ratio between difference in costs and difference in QALYs (Quality Adjusted Life Years, from EQ-5D) among the treatment groups, during the first 2 years after diagnosis
Rete Oncologica Piemonte, Valle d'Aosta
Other
START (Active Surveillance or Radical Treatment for Newly Diagnosed Patients With a Localized, Low Risk, Prostate Cancer): an Epidemiological Study of the Oncology Network of Piemonte and Valle d'Aosta (Italy)
Acronym: START
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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