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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexMale
Age18-80
SponsorChinese University of Hong Kong

About this trial

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.

Eligibility criteria

Qualifiers

Adult men 18-80 years old

With histological proven prostate cancer or clinically diagnosed to have prostate cancer,

Planned for ADT for at least 1 year

Disqualifiers

Subjects with established major atherosclerotic cardiovascular disease (ASCVD) as defined by a recent acute coronary syndrome within the past 12 months, a history of myocardial infarction other than the recent acute coronary syndrome event, a history of ischemic stroke, and symptomatic peripheral arterial disease (defined as history of claudication with ankle-brachial index <0.85 or previous revascularization or amputation

Prior neoadjuvant or adjuvant hormone therapy within 1 year before

Refuse or unable to give written informed consent

Participation in an investigational program with interventions outside of routine clinical practice

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

130 Participants
are grouped into 1 trial group