Chemokeyp: A Feasibility Check for Quick Safety Data in Cancer Care

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Chemokeyp is an observational feasibility study that uses a secure ED-oncology interface for patients on chemotherapy. When patients visit the Emergency Department, staff can scan a QR code on a medical-alert wristband to access a brief, predefined safety questionnaire about potential adverse events. The portal collects structured safety data for research and signal detection, without interacting with the patient’s electronic health record or altering standard clinical care. Data entry is limited to specific fields and is intended to test the practicality and timeliness of real-time safety reporting in unscheduled care settings. The study is conducted at St Vincent’s University Hospital in Dublin and focuses on safety data capture rather than clinical decision support.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patient undergoing treatment for cancer at SVUH

Exclusion Criteria:

* Presence of a condition(s) or diagnosis, either physical or psychological, or physical exam finding that precludes participation (inability to give informed consent)

Where it's running

• St Vincent's University Hospital
  Dublin, Dublin, Ireland Recruiting

Study contacts

• Study coordinator: Rosa F McNamara, FRCEM FRCPI
• Email: rosamcnamara@svhg.ie
• Phone: +353857111841

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.