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TerminatedNCT02538809Updated Feb 13, 2025

Novel mRNA-based Urine Test for Bladder Cancer in Spinal Cord Injury Individuals

An observational study in Bladder Cancer and Spinal Cord Injury, sponsored by Swiss Paraplegic Research, Nottwil. Terminated at 1 site in Switzerland. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-02-13.

Sponsored by Swiss Paraplegic Research, Nottwil · Observational

Why this study was terminated
insufficient recruitment
Study type
Observational
Model
Case-control
Time perspective
Cross-sectional
Enrollment
50
Ages
18 Years and older
Sex
All
01

Study summary

Bladder cancer is a well-recognized complication in spinal cord injury (SCI) individuals. The observed incidence rates in SCI individuals are considerably higher compared to the general population. Bladder cancer in SCI individuals tends to present at an earlier age compared to the general population. Furthermore, bladder cancer in SCI individuals is more commonly invasive and at a more advanced stage at the time of diagnosis compared to bladder cancer in the general population. Individuals with bladder cancer commonly present with hematuria and other urinary symptoms. The gold standard for diagnosis is cystoscopy. However in SCI individuals, hematuria may get attributed to catheter irritation or trauma or an urinary tract infection. Furthermore, the bladder wall commonly presents with various changes under cystoscopic examination masking the presence of a bladder wall mass. Thus, diagnosis of bladder cancer in SCI individuals can be complicate.

There is a novel test available (GeneXpert® Bladder Cancer Detection, Cepheid International, Sunnyvale, CA, USA) for the measurement of mRNA bladder tumor markers in the urine. The diagnostic accuracy of this test has been investigated in non-SCI individuals with symptoms suspicious for bladder cancer. The test showed high sensitivity and specificity values and is thus a promising diagnostic or screening tool.. However, the diagnostic accuracy of the test has not yet been investigated in SCI individuals.

The primary objective of the proposed study is to investigate whether urine mRNA tumor marker levels in spinal cord injury individuals with symptoms and findings suspicious for bladder cancer are a discriminator between individuals suffering from bladder cancer and those not suffering from cancer.

Individuals presenting with symptoms suspicious of bladder cancer will undergo ultrasonic and cystoscopic examination of the bladder. An urine sample will be taken, and the bladder will be flushed for collecting a bladder fluid sample. In patients with bladder wall findings suspicious of cancer, a bladder wall biopsy will be taken, according to clinical standard practice. The bladder fluid and the bladder wall biopsy will be submitted for cytology and histopathology examination, respectively. Tumor mRNA levels will be measured in the urine sample.

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Conditions studied

  • Bladder Cancer
  • Spinal Cord Injury
03

In context

Urinary Bladder Neoplasms

1,649 studies on the registry are indexed under Urinary Bladder Neoplasms; 427 are open to participants now.

This study's enrollment of 50 is below the median of 179 across 385 observational studies indexed under Urinary Bladder Neoplasms.

Browse Urinary Bladder Neoplasms studies →

Lead sponsor

Swiss Paraplegic Research, Nottwil is the lead sponsor of 70 studies on the registry; 9 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

individuals presenting with symptoms or clinical findings suspicious for bladder cancer at a tertiary urologic referral center

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Symptoms suspicious of bladder cancer (haematuria, ultrasonic and cystoscopy findings)
  • Chronic spinal cord injury for a minimum of 3 years
  • Informed Consent as documented by signature

Exclusion criteria

Exclusion Criteria:

  • Age \< 18 years
  • History of bleeding disorder
  • Bladder augmentation
  • Acute, symptomatic urinary tract infection
  • Pregnancy
  • Urolithiasis
  • Previous intravesical treatment (e.g. bladder irrigation, botulinum toxin injection) \< 2 weeks)
05

Study design

Observational model
Case-control
Time perspective
Cross-sectional
Enrollment
50 participants (actual)
Patient registry
No

Interventions

  • Othermeasurement of tumor mRNA concentration in urine

    bed-side test of tumor mRNA concentration in urine

06

What researchers measure

Primary outcomes

  1. urine tumor mRNA concentration

    Time frame: 1 day

Secondary outcomes

  1. cystoscopic findings of bladder wall

    findings suspicious of bladder cancer present: yes / no

    Time frame: 1 day

  2. microscopic identification of cells in bladder fluid sample

    Time frame: 1 day

  3. histopathologic examination of the bladder wall biopsy

    diagnosis of bladder cancer: yes / no

    Time frame: 1 day

07

Study locations

1 site
  • Swiss Paraplegic Centre
    Nottwil, Canton of Lucerne CH-6207, Switzerland
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 13, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02538809
Lead sponsor
Swiss Paraplegic Research, Nottwil
Responsible party
Sponsor
First posted
Sep 2, 2015
Start date
Aug 13, 2018
Primary completion
Dec 31, 2024
Completion
Dec 31, 2024
Last update
Feb 13, 2025

Study contacts

Jens Wöllner
principal investigator · Schweizer Paraplegiker-Zentrum Nottwil

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is terminated, as verified in Feb 2025. You cannot join it, but the record below documents what was studied.

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