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Study identifier: NCT07592234 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Chemokeyp: A Feasibility Study for Realtime Safety Data-Capture for Potential Serious Adverse Drug Events

Condition: Serious Adverse Events · Patient Safety · Pharmacovigilance  ·  Sponsor: St Vincent's University Hospital, Ireland

PhaseN/A
Planned participants100
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

Chemokeyp is a feasibility study testing a secure ED-Oncology interface for patients receiving chemotherapy who may present to unscheduled care with possible treatment-related complications. Participants are enrolled through Oncology and issued a medical-alert-style wristband with a QR code. If they attend the Emergency Department, staff can scan the QR code, access a generic study landing page, and, after SVUH authentication, complete a short structured checklist about possible serious adverse events such as infection, chest pain, vomiting, syncope, or other red-flag symptoms. The platform is designed as a secure research data-capture portal, not an electronic health record or clinical documentation system. It does not read from or write to the hospital EHR, does not provide clinical decision support, and does not change usual clinical care. Data entered by ED clinicians are limited to predefined structured fields for research and safety-signal feasibility purposes. The study will assess whether ED clinicians can complete the checklist in real time, whether the information can support earlier notification to the research/trial team, and whether this data accurately corresponds with verified serious adverse events. If feasible, Chemokeyp could help improve communication between Oncology, Emergency Medicine, and trial teams, supporting safer care for patients on chemotherapy and informing future development of ED-oncology digital safety tools.

This description comes directly from the study's public registry record.

Talk to the study team

Rosa F McNamara, FRCEM FRCPI  ·  +353857111841  ·  rosamcnamara@svhg.ie

Always discuss trial participation with your own doctor first.

Locations (1)

St Vincent's University HospitalDublin, Dublin, IrelandRecruiting

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Source record: clinicaltrials.gov/study/NCT07592234