A Study of Ward Admissions for Haematuria
WASHOUT
Ward AdmiSsion of Haematuria: an Observational mUlticentre sTudy
1 other identifier
observational
1,050
1 country
1
Brief Summary
This multicenter, prospective observational study will evaluate national and international practice variations (if present) in the emergency management of patients admitted to hospital with haematuria, inform a consensus guideline for best practice and provide evidence to design an implementation study to optimise haematuria management pathway.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2024
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2024
CompletedFirst Submitted
Initial submission to the registry
March 14, 2025
CompletedFirst Posted
Study publicly available on registry
February 9, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2026
CompletedFebruary 9, 2026
February 1, 2026
2.3 years
March 14, 2025
February 3, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Length of inpatient stay
Number of calendar days between the day of admission in the index hospital admission episode and the day of discharge from the hospital.
At 90 days
Secondary Outcomes (5)
Mortality rate
At 90 days
Readmission rate
At 90 days
Time to definitive diagnosis
At 90 days
Number of days alive and out of hospital
At 90 days.
Resource use
At 90 days
Study Arms (1)
Prospective, obersational cohort (single cohort study)
All patients meeting above defined inclusion and exclusion criteria. This study will take place in urological secondary and tertiary care centres internationally. The study will be conducted in centres that agree to participate in the study and meet the study's inclusion criteria below.
Interventions
The study hypothesis is that there is significant international and national variation in the diagnostic workup and management of patients requiring admission to the hospital with haematuria. Increased length of stay and poor outcomes in terms of mortality and healthcare costs are associated with management practices. The CRF will collect datapoints on inpatient work-up and management.
Eligibility Criteria
Patients will be included consecutively if they are over 18 years of age and admitted to a participating secondary care centre as an emergency with haematuria under the primary or joint care of the urology team.
You may qualify if:
- Patients are included if they are over 16 years of age or older and admitted to a participating urological secondary care centre
- admitted as an emergency with haematuria as the primary or secondary diagnosis under the primary or joint care of urology
You may not qualify if:
- any patients under 16 years of age
- patients with catheter-related urethral trauma (defined as haemturia immediately after insertion of a urethral catheter that was documented as traumatic by the clinician, with no previous history of haemturia prior to catheter insertion)
- patients that are in hospital less than 24 hours.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
BURST
London, United Kingdom
Related Links
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 14, 2025
First Posted
February 9, 2026
Study Start
January 1, 2024
Primary Completion
April 30, 2026
Study Completion
April 30, 2026
Last Updated
February 9, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share