EVEREST-HN 1: EVolution of a patiEnt-REported Symptom-based Risk Stratification sySTem
NCT ID: NCT05909020
Last Updated: 2023-10-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
165 participants
OBSERVATIONAL
2023-03-17
2023-11-30
Brief Summary
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Our methodology includes six interlinked work packages to deliver our aim, with EVEREST-HN 1 encompassing the first of these and seeking to optimise a patient-reported symptom inventory for HNC and outline requirement specification for the SYmptom iNput Clinical (SYNC) system.
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Detailed Description
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Conditions
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Study Design
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OTHER
PROSPECTIVE
Study Groups
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Patients
Approximately 150 adults referred for suspected HNC will be recruited.
No intervention.
No intervention.
Staff
Approximately 15 ENT and Maxillofacial) clinicians will be recruited.
No intervention.
No intervention.
Interventions
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No intervention.
No intervention.
Eligibility Criteria
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Inclusion Criteria
* Adults ≥ 18 years referred via suspected HNC pathway without previous history of HNC
* Participants willing and able to give informed consent for participation in the study.
Clinicians:
* Staff at participating sites involved in the diagnostic pathway for people with suspected HNC.
18 Years
ALL
No
Sponsors
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University of Leeds
OTHER
Royal Marsden NHS Foundation Trust
OTHER
Responsible Party
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Principal Investigators
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Vinidh Paleri
Role: STUDY_CHAIR
Royal Marsden NHS Foundation Trust
Locations
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Leeds Teaching Hospitals NHS Trust
Leeds, , United Kingdom
Liverpool University Hospitals NHS Foundation Trust
Liverpool, , United Kingdom
Luton & Dunstable University Hospital
Luton, , United Kingdom
Oxford NHS Foundation Trust
Oxford, , United Kingdom
Countries
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Central Contacts
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Facility Contacts
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Unknown Unknown
Role: primary
Shirley Pringle
Role: primary
Nithin George
Role: primary
Iqbal Mohammed
Role: primary
Other Identifiers
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CCR5683
Identifier Type: -
Identifier Source: org_study_id
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