Emergency Department TriageNCT06933550
PREMEDICAL is a Clinical Investigation Aiming to Create a Data Basis That Can be Used to Enrich Information Collected in the Course of the Classic Patient Journey. Patients in the Emergency Department Will be Asked to Answer Patient-related and Symptom-oriented Questions. Minimum Age is 18 Years
An observational study of Emergency Department Triage, run by XUND Solutions GmbH at 1 site in Austria.
Trial summary
The goal of this clinical investigation is to create a new type of data basis that can be used to enrich information collected in the course of the classic patient journey, such as medical history forms and discharge letters. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Emergency Department Triage
- How many people
- 351 participants
- Where
- 1 siteAustria
- Study dates
- 4 Jul 2025to 6 May 2026
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Adult, Older adult
Study population: German speaking, at least 18 years old, all gender patients in the emergency department (triage category 3, 4, or 5).
Who may be able to join
- a signed informed consent form;
- signed consent and admission to the emergency department of the emergency medicine clinic
- Triage category 3, 4 or 5 based on the triage procedure according to the Manchester triage system used in Austria
- the physical and mental ability to operate the tablet and answer the questions
- 18 years of age or older;
- knowledge of the German language.
Who cannot join
- not meeting all inclusion criteria
Trial locations and contacts
1 site in 1 country.
About this study
Official title: FFG PREMEDICAL (Clinical Investigation of a Medical Device According to MDR Article 82, Para.1 and Austrian Law §13 Para. 3 MPG, BGBI. I No. 122/2021 - Study Without Influence on Diagnostics/Therapy)
The goal of this clinical investigation is to create a new type of data basis that can be used to enrich information collected in the course of the classic patient journey, such as medical history forms and discharge letters. Therefore, it is planned to collect new, patient-related and symptom-oriented data on site and directly from patients in the emergency department (female/male; at least 18 years old).
The main question it aims to answer is:
Read more
- Can a detailed medical history with additional enriched information from XUND improve the quality of outpatient care?
Selected patients in the waiting area of the emergency department will record their symptoms on a tablet and answer the questions asked about their symptoms.
- Conditions
- Emergency Department Triage
- Keywords
- XUND, emergency department, symptom check, patient journey
- Medical subject headings
- Emergencies
What is being measured
The primary outcome is the main question the study is designed to answer.
XUND Symptom Checker
The fundamental element of the proposed project is the aggregation of novel, patient-related and symptom-oriented data on-site and directly from patients in the emergency department. The objective of this study is to establish a novel type of data basis, with the potential to enhance the information collected during the conventional patient journey, including medical history forms and discharge letters. XUND's Symptom Check, which has been certified as a class IIa medical device, will be used to collect the data. Selected patients in the emergency waiting area record their symptoms on a tablet and answer the questions asked. The Symptom Check is powered by an AI-driven medical knowledge base of 520+ conditions and 21,000+ symptom variants.
Measured: through investigation completion, an average of 1 year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Apr 2025
- Study start4 Jul 2025
- Primary completion6 May 2026
- Study completion6 May 2026
Why it stopped: Funding issues, recruitment targets not met
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Emergency Department TriageStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case only
- Time perspective
- Cross-sectional
- Enrolment
- 351 participants (actual)
Sponsor and investigators
- Lead sponsor
- XUND Solutions GmbH
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- Medical University of Graz
- Responsible party
- Sponsor
- Investigators
- Lars-Peter Kamolz, Univ. Prof. Dr., Principal investigator, Medizinische Universität Graz, Universitätsklinik für Chirurgie
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06933550
- Sponsor's protocol ID
- 892459
- Other IDs
- 102478757
- Status last verified
- Oct 2026
- First submitted
- 8 Apr 2025
- Last updated
- 21 Oct 2026
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 21 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- FFG PREMEDICAL (Clinical Investigation of a Medical Device According to MDR Article 82, Para.1 and Austrian Law §13 Para. 3 MPG, BGBI. I No. 122/2021 - Study Without Influence on Diagnostics/Therapy)
- ClinicalTrials.gov ID
- NCT06933550
- Acronym / sponsor ID
- 892459
- Conditions
- Emergency Department Triage
- Keywords
- XUND, emergency department, symptom check, patient journey
- Study type
- Observational
- Recruitment status
- TerminatedReason stopped: Funding issues, recruitment targets not met
- Enrolment
- 351 participants (actual)
- Lead sponsor
- XUND Solutions GmbHIndustry (pharma, biotech, devices)
- Collaborators
- Medical University of Graz
- Study start
- 4 Jul 2025 (actual)
- Primary completion
- 6 May 2026 (actual)
- Study completion
- 6 May 2026 (actual)
- First posted
- 18 Apr 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this clinical investigation is to create a new type of data basis that can be used to enrich information collected in the course of the classic patient journey, such as medical history forms and discharge letters. Therefore, it is planned to collect new, patient-related and symptom-oriented data on site and directly from patients in the emergency department (female/male; at least 18 years old).
The main question it aims to answer is:
- Can a detailed medical history with additional enriched information from XUND improve the quality of outpatient care?
Selected patients in the waiting area of the emergency department will record their symptoms on a tablet and answer the questions asked about their symptoms.
Study design
- Observational model
- Case only
- Time perspective
- Cross-sectional
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Age groups
- Adult, Older adult
- Study population
- German speaking, at least 18 years old, all gender patients in the emergency department (triage category 3, 4, or 5).
Key inclusion criteria (6 listed)
- a signed informed consent form;
- signed consent and admission to the emergency department of the emergency medicine clinic
- Triage category 3, 4 or 5 based on the triage procedure according to the Manchester triage system used in Austria
- the physical and mental ability to operate the tablet and answer the questions
- 18 years of age or older;
Key exclusion criteria (1 listed)
- not meeting all inclusion criteria
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
XUND Symptom Checker
Time frame: through investigation completion, an average of 1 year
The fundamental element of the proposed project is the aggregation of novel, patient-related and symptom-oriented data on-site and directly from patients in the emergency department. The objective of this study is to establish a novel type of data basis, with the potential to enhance the information collected during the conventional patient journey, including medical history forms and discharge letters. XUND's Symptom Check, which has been certified as a class IIa medical device, will be used to collect the data. Selected patients in the emergency waiting area record their symptoms on a tablet and answer the questions asked. The Symptom Check is powered by an AI-driven medical knowledge base of 520+ conditions and 21,000+ symptom variants.
Results and safety
The study was stopped early (reason given: Funding issues, recruitment targets not met). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 21 Oct 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Lars-Peter Kamolz, Univ. Prof. Dr. principal investigator
Medizinische Universität Graz, Universitätsklinik für Chirurgie
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Emergency Department Triage, run by XUND Solutions GmbH at 1 site in Austria.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 21 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Austria. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study was stopped early (reason given: Funding issues, recruitment targets not met). Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
XUND Symptom Checker (time frame: through investigation completion, an average of 1 year). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Oct 2026; AzTrials last refreshed its copy on 6 Nov 2026.