Safely Reduce Cystoscopic Evaluations for Hematuria Patients

Bladder Cancer Clinical Trial

— SeARCH  

Official title:

Safely Reduce Cystoscopic Evaluations for Hematuria Patients

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06026189
• Other study ID #: Erasmus MC
• Status: Recruiting
• Phase: N/A
• Start date: May 31, 2023
• Est. completion date: May 31, 2027

Study information

• Verified date: August 2023
• Source: Erasmus Medical Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The SeARCH-trial assess the clinical impact of a molecular urine test as a 'urine-first' strategy in the diagnostic workup of patients presenting with microscopic hematuria.

Description:

Microscopic hematuria (MH) can be a sign of an underlying disease, including malignancy of the urinary tract, and is reason for referral to a urology clinic. The current standard diagnostic workup for MH patients includes visual inspection of the bladder by cystoscopy and upper tract imaging to rule out the presence of a tumor in the urinary tract. However, the a priori risk of cancer in patients with MH is only 2-5%. Consequently, 95% of MH patients unnecessarily undergo invasive procedures, which are: I) uncomfortable and stressful for patients, II) has a significant impact on limited available (financial) resources and III) a CT scan is accompanied by exposure to ionizing radiation.

Previously we developed a molecular urine assay to detect urinary tract cancer in hematuria patients that had robust diagnostic performance; a negative predictive value >99%, sensitivity, and specificity >90%. The SeARCH-trial evaluates the clinical impact of a urine assay as a 'urine-first' strategy, meaning that only patients with an abnormal urine test results undergo invasive diagnostics. In this multicenter stepped-wedge cluster randomized trial we compare clinical outcomes by using a 'urine-first' strategy to 'care-as-usual', which is a cystoscopy and upper tract imaging in all patients presenting with MH. In addition, we assess patients' preferences, patients reported outcome measurements, and healthcare costs to show that a 'urine-first' strategy improves patients' quality of life and results in a more appropriate use of limited available resources.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 1100
• Est. completion date: May 31, 2027
• Est. primary completion date: May 31, 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Microscopically confirmed microscopic hematuria of voided urine defined as =3 erythrocytes per high power field

• Male patients =40 years

• Female patients =50 years

Exclusion Criteria:

• History of urothelial bladder- or urinary tract cancer

• Presence of macroscopic (visible) hematuria

• Woman who is or may be pregnant

Related Conditions & MeSH terms

• Bladder Cancer
• Carcinoma, Transitional Cell
• Hematuria
• Urinary Bladder Neoplasms
• Urothelial Carcinoma
• Urothelial Neoplasm

Intervention

Diagnostic Test:
• urine-first strategy
Only patients with an abnormal urine test result undergo a diagnostic workup, i.e. cystoscopy and upper-tract imaging.

Locations

Country	Name	City	State
Netherlands	SeARCH-trial Pijpers	Rotterdam

Sponsors (1)

Lead Sponsor	Collaborator
Erasmus Medical Center

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The primary aim of the SeARCH-trial is to assess the clinical impact of implementing a molecular urinary assay as a 'urine-first' strategy, in the diagnostic workup of patients presenting with microscopic hematuria.	The net benefit is defined as the proportion of patients who were diagnose with urinary tract cancer within 1 year after initial diagnostic work-up in the population (true positives) subtracted by the proportion of patients that underwent diagnostic evaluations without an abnormal finding (false positives). The latter is multiplied by the decision threshold, which represents the estimated harms of the diagnostic intervention, such as patients' burden and use of available resources, against the harms of an outcome event, i.e. missing a urinary tract tumor.	1 year
Secondary	The number of cystoscopies and upper tract imaging modalities (CT or ultrasound) when using a 'urine-first' strategy versus 'care-as-usual'		1 year
Secondary	Cost-effectiveness analysis	This will be performed according to the Dutch guideline by administering validated questionnaires.	Questionnaires are administered at baseline, 3, 6, and 12 months.
Secondary	Patient reported outcome measurements (PROMs)	Patient-reported outcome measurements (PROMs) are assessed for patients undergoing cystoscopy and urine collection.	Questionnaires are administered at baseline, 3, 6, and 12 months.