Prostate Cancer Clinical Trial
Official title:
The Effects of Prostate Cancer on Brain Function: a Prospective Cohort Study
NCT number | NCT05737004 |
Other study ID # | EF2023-01 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | April 13, 2023 |
Est. completion date | April 1, 2024 |
To explore whether the patients with prostate cancer have functional changes in specific brain areas and changes in psychological and mental characteristics compared with the patients without prostate cancer.
Status | Recruiting |
Enrollment | 250 |
Est. completion date | April 1, 2024 |
Est. primary completion date | February 12, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 18 Years to 80 Years |
Eligibility | Inclusion Criteria: 1. Between the ages of 18 and 80 2. Patients with prostate biopsy; 3. No history of other malignant tumors; 4. Exclude other malignant tumors; 5. Fully understand the clinical trial protocol and sign informed consent; Exclusion Criteria: 1. magnetic resonance contraindications; 2. symptomatic acute or chronic inflammation of the prostate; 3. Patients with brain trauma or brain disease; 4. Patients who have died of other malignancies in the past or are currently suffering from other malignancies; 5. Patients judged by the investigator to be unfit to participate in the clinical trial; |
Country | Name | City | State |
---|---|---|---|
China | Shanghai East Hospital, Tongji University School of Medicine | Shanghai | Shanghai |
Lead Sponsor | Collaborator |
---|---|
Shanghai East Hospital |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The evaluation of Magnetic Resonance(MR) | To compare the differences in rs-fMRI measures (Amplitude of low frequency fluctuations , Regional Homogeneity and Functional Connectivity ) between prostate cancer group and Non-prostate cancer group. | Within 1 week before biopsy | |
Secondary | Assessment of anxiety status | Zung Self Rating Anxiety Scale was used to assess anxiety status.By comparing the final score, less than or equal to 10 is considered healthy, and more than 10 is considered abnormal. | Within 1 week before biopsy | |
Secondary | Assessment of depressive status | Beck Depression Inventory-II was used to assess depressive status.By comparing the final scores, a score of 50 or less is considered healthy and a score of 50 or more is considered abnormal. | Within 1 week before biopsy |
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