Fact CheckerSign in

NCT05180942Active, not recruiting

Statins and prOgression of Coronary atheRosclerosis in melanomA Patients Treated With chEckpoint inhibitorS

Source: ClinicalTrials.gov · Last updated 8 Oct 2026

Brief summary (registry, in English)

This study is a prospective observational study evaluating the natural history of coronary plaque burden in participants with melanoma treated with ICI. The study will be conducted at various sites across Australia.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
130 (estimated)
First submitted
11 Nov 2021
Start date
7 Nov 2022
Primary completion date
Dec 2026
Lead sponsor
Monash University
NCT number
NCT05180942

What you commit to

  • Study type: Observational
  • Planned participants: 130
  • From 7 Nov 2022 to the primary completion date, Dec 2026
  • 12 sites 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.

Other illness

  • Known clinically manifest cardiovascular disease
  • Estimated glomerular filtration rate of \<45 mL/min calculated using the Chronic Kidney Disease Epidemiology Collaboration equation
  • Severe liver disease or cirrhosis
  • History of any other malignancy within the past 5 years in addition to melanoma with the exception of non-melanoma skin cancers
  • Evidence of any other clinically significant non-cardiac disease or condition that, in the opinion of the Investigator, would preclude participation in the study
  • Major allergy to iodine

Other

  • Female participants must not be pregnant, breastfeeding or plan to become pregnant during the study.
  • Prognostic factors associated with an expected survival less than 18 months at Investigators' discretion (e.g. unresectable brain metastases)
  • Participation in another clinical trial that does not allow participation in multiple trials at the same time

Who the study is looking for

  • Capable of providing informed consent and willing to adhere to all protocol requirements
  • patients aged \> or equal to 40 years
  • Histologically confirmed melanoma of any stage planned for, commenced, or completed treatment with ICI
  • having acceptable imaging quality deemed by the core laboratory
  • Investigator believes that the participant is willing to adhere to all protocol requirements, including returning for follow up CTCA.

Age in the registry: 40 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (12)

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

SiteCityCountrySite status
Bundaberg Base Hospital
Coordinator of this site? Confirm its status
BundabergAustraliaUnknown status
Monash Health
Coordinator of this site? Confirm its status
ClaytonAustraliaUnknown status
Peninsula Health
Coordinator of this site? Confirm its status
FrankstonAustraliaUnknown status
Hervey Bay Hospital
Coordinator of this site? Confirm its status
Hervey BayAustraliaUnknown status
Ipswich Hospital
Coordinator of this site? Confirm its status
IpswichAustraliaUnknown status
Nepean Hospital
Coordinator of this site? Confirm its status
KingswoodAustraliaUnknown status
Cabrini Health
Coordinator of this site? Confirm its status
MalvernAustraliaUnknown status
Peter MacCallum Cancer Centre
Coordinator of this site? Confirm its status
MelbourneAustraliaUnknown status
Mildura Public Base Hospital
Coordinator of this site? Confirm its status
MilduraAustraliaUnknown status
Toowoomba Hospital
Coordinator of this site? Confirm its status
ToowoombaAustraliaUnknown status
Calvary Mater Newcastle
Coordinator of this site? Confirm its status
WaratahAustraliaUnknown status
Queen Elizabeth Hospital
Coordinator of this site? Confirm its status
Woodville SouthAustraliaUnknown status

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