Home Monitoring of Complete Blood Count Performed by Patients - a Pilot Study on the Implementation Process in South Baltic Countries.

Recruiting Observational Study
Cancer Cancer-related Problem/Condition Chemotherapy Chemotherapy-induced Neutropenia Chemotherapy Induced Anaemia Chemotherapy Induced Thrombocytopenia
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
265 (estimated)
Sponsor
Pomeranian Medical University Szczecin · Other
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About This Trial
Introduction: The number of diagnosed cancers is systematically increasing every year. Cancer patients need to undergo regular blood tests to monitor safety and eligibility for treatment. In case of poor blood results, the chemotherapy session must be omitted. For patients living far from the center, this means unnecessary travel with involvement of helpers, additional costs, increased potential …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * legally competent patients * aged 18 or older * diagnosed with cancer (ICD-10: C00\* - C97\*) * enrolled at the Department of Oncology/Hematology for outpatients * participants who are willing and able to give informed consent for participation in the study * participants shou…
Contacts

Bartłomiej Baumert, MD, PhD, DSc

+48 91 4250428

bartlomiej.baumert@pum.edu.pl

CONTACT

Karolina Szmuc, MSc

+48 91 4250428

karolina.szmuc@usk1.szczecin.pl

CONTACT