CI

At a glance

ClinicalIndex Comparison Record
N/ARecruiting· 15,000 target
Drug / intervention
No interventionother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03344835
NCT03344835N/ARecruitingOn TrackUpdated 13mo ago
Long Recruiting

A Comprehensive Assessment of the Physical and Biological Effects of Patients With Prostate Cancer in Hong Kong

Chinese University of Hong Kong·observational·Posted Nov 17, 2017·Updated May 6, 2025

In Brief

An observational study evaluating No intervention for Prostate Cancer. Currently recruiting, targeting 15,000 participants across 1 site.

Detailed Summary

Prostate cancer (PCa) is ranked 3rd in annual incidence of male cancer and ranked 5th for cancer-related death in men in Hong Kong which accounts for about 9.1 deaths per 100,000 men in 2011. Its incidence is rising rapidly, almost tripled in the past 10 years. In Hong Kong, the two main screening methods for PCa are digital rectal examination (DRE) and serum prostate-specific antigen (PSA) level blood test, and the gold standard of diagnosis of PCa is transrectal ultrasound (TRUS) with prostate biopsy. For those who diagnosed with PCa, there are different kinds of managements depending on patient's age group and disease stage. Watchful waiting is for older patients who presents with low-risk prostate cancer. And active surveillance is applicable to patients who are eligible for potentially curative management. While radiotherapy or radical prostatectomy are recommended as curative management for early stage PCa, androgen deprivation therapy (ADT) is the main treatment modality for advanced or recurrent prostate cancer. Advanced prostate cancer that recurrence is called castration refractory prostate cancer (CRPC). There are many new agents, including second line hormonal therapy, chemotherapy, androgen biosynthesis inhibitors, immunotherapy, bone targeting agents etc., available for the further management. In this study, investigators would like to establish a local prostate cancer registry to facilitate the collection of clinical information and outcomes of prostate cancer management. Hopefully, this registry can provide information regarding the epidemiology, natural history, and treatment outcomes of local prostate cancer. The information would be helpful for research, public education, health care planning and also international collaboration. Ultimately, patients and public would be benefited from these works.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsProstate Cancer
CountriesHong Kong
Collaborators--

Timeline

N/ARecruiting
20162017201820192020202120222023202420252026202720282029203020312032203320342035203620372038203920402041
First PostedNov 17, 2017
Enrollment StartJan 1, 2016
Primary CompletionDec 31, 2035
Study CompletionDec 31, 2040
TodayJul 1, 2026
Enrollment to primary: 20 yearsPosted 8.6 years agoPrimary completion in 9.5 years

Interventions

No interventionother