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Fast-Track Cardiovascular Assessment for Suspicion of Cardiovascular Events on Immunecheckpoint Inhibitors

Fast-Track Cardiovascular Assessment for Suspicion of Cardiovascular Events on Immunecheckpoint Inhibitors: Prospective Cohort Study.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05799898
Acronym
FAST-TRACK
Enrollment
200
Registered
2023-04-05
Start date
2022-03-01
Completion date
2030-01-01
Last updated
2023-04-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer, Cardiovascular Complication, Immune Checkpoint Inhibitor, Immune-related Adverse Event

Brief summary

Prospective study cohort on patients addressed for suspected cardiovascular event on immune checkpoint inchibitors. Longitudinal prospective single center cohort. Inclusion criteria: all patient willing to particiupate seen in the cardio-oncology unit at our institution for the suspicion of heart failure, atherosclerosis related event, Tako Tsubo, arrhymias, pericarditis, myocarditis on antiPD1, antiPDL1, or antiCTLA4 immune checkpoint inhibitors. Description of patients characteristics, investigations, diagnosis after multidisciplinary meeting, outcomes.

Interventions

OTHERNo intervention for research purposes only

No intervention for research purposes only

Sponsors

Institut Mutualiste Montsouris
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* all patient referred to the cardio oncology unit for suspected immune related cardiovascular complication on immune checkpoint inhibitors

Exclusion criteria

* none

Design outcomes

Primary

MeasureTime frameDescription
Major cardiovascular event12 monthsComposite endpoint: acute coronary syndrome, myocarditis, pericarditis, heart failure, Taki Tsubo, ventricvular arrhymias

Countries

France

Contacts

Primary ContactIsabelle Sauret
isabelle.sauret@imm.fr+33156616705
Backup ContactNathalie Bass
nathalie.bass@imm.fr

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 4, 2026