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NCT06163924Recruiting

The Effect of Multidisciplinary Care Approach on CV Risk Modification in CaP Patients Receiving ADT

To Investigate the Effect of Multidisciplinary Care Approach on Cardiovascular Risk Modification in Prostate Cancer Patients Receiving Androgen Deprivation Therapy

Source: ClinicalTrials.gov · Last updated 28 Oct 2026

Brief summary (registry, in English)

Prostate cancer is characterised by its slow progression nature, and even for metastatic disease, the 5-year survival is up to 30%. While ADT can effectively control disease, there is increasing evidence suggesting that it can also result in many adverse cardiovascular side effects on the patients, and these effects are particularly important due to the prolonged survival of these patients. There are suggestions that close cardiovascular (CV) monitoring will help to reduce cardiovascular risk and related morbidities. However, there is limited data to show the positive impact of these monitoring could reducing CV risk and morbidities. Moreover, information regarding the optimal follow-up approach and schedule is also lacking. Therefore, there is a need to have more information on the approach to monitoring the CV risk and the real-life impact of this monitoring on our patients. Patients diagnosed with prostate cancer and plan to receive ADT are invited to participate in this study to assess the potential benefit of multidisciplinary care approach to CV risk modification.

Status (registry)
Recruiting
Study type
Observational
Enrollment
300 (estimated)
First submitted
1 Dec 2023
Start date
10 Dec 2023
Primary completion date
31 Dec 2028
Lead sponsor
Chinese University of Hong Kong
NCT number
NCT06163924

What you commit to

  • Study type: Observational
  • Planned participants: 300
  • From 10 Dec 2023 to the primary completion date, 31 Dec 2028
  • 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.

Prior treatment

  • Prior neoadjuvant or adjuvant hormone therapy within 1 year before

Other

  • Refuse or unable to give written informed consent
  • Participation in an investigational program with interventions outside of routine clinical practice

Who the study is looking for

  • Adult men ≥18 years old
  • With histological proven prostate cancer or clinically diagnosed to have prostate cancer,
  • Planned for ADT for at least 1 year

Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The Chinese University of Hong Kong
Coordinator of this site? Confirm its status
Hong KongHong Kong SAR ChinaRecruiting

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