Prostate Cancer Metastatic Clinical Trial
Official title:
Zhongshan Hospital, Fudan University
NCT number | NCT03988686 |
Other study ID # | B2019-065 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | April 1, 2019 |
Est. completion date | March 31, 2022 |
This study is to examine whether radical prostatectomy can impact survival and quality-of-life in men with oligo-metastatic prostate cancer.
Status | Recruiting |
Enrollment | 120 |
Est. completion date | March 31, 2022 |
Est. primary completion date | March 31, 2021 |
Accepts healthy volunteers | No |
Gender | Male |
Age group | 18 Years to 75 Years |
Eligibility |
Inclusion Criteria: - Participants is willing and able to give informed consent for participation in the study - Male aged 19-75 years. - Diagnosed with oligo-metastatic prostate cancer (1-3 skeletal lesions on bone specific imaging, no visceral metastases). - Locally resectable tumor (clinical/radiological stage T1-T3). - Eastern Cooperative Oncology Group (ECOG) performance status 0-1. - Suitable for radical prostatectomy within 12 months of starting standard care. Exclusion Criteria: - Contraindications to radical prostatectomy. - Visceral metastases. - Prior radiotherapy to the abdomen/pelvis or to skeletal metastases. - Any systemic therapy of prostate cancer (including standard care) for 12 or more months prior to enrollment. - Current involvement in other interventional research. |
Country | Name | City | State |
---|---|---|---|
China | Zhongshan Hospital, Fudan University | Shanghai | Shanghai |
Lead Sponsor | Collaborator |
---|---|
Fudan University | University College, London |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | the time to castrate resistance | The time to treatment failure defined as castrate resistance will be recorded via routine patient follow-up interviews. | 36 months after randomization | |
Secondary | Quality of life in patients post-randomization | EuroQOL 5 dimensions 5 levels (EQ-5D-5L) questionnaire will be used to assess quality of life in patients after randomization with different treatments. This is designed to measure health-related quality of life. It consists of a questionnaire and a visual analogue scale. The subjects in 5 dimensions i.e. mobility, self-care, usual activities, pain/discomfort and anxiety/depression are asked to grade their own current level of function in each dimension into one of five levels of disability (i.e. I have no problems waling about, slight problems, moderate problems, severe problems, or unable to walk). This tool also has an overall health scale where the rater selects a number between 1-100 to describe the condition of their health, 100 being the best imaginable. | three month post randomization |
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