BWash: Bladder Washing Cytology for Detection of Urothelial Carcinoma Using Catheter or Flexible Cystoscope: Which is Better?

Sponsor
Centre Hospitalier Universitaire Vaudois (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05643807
Collaborator
(none)
414
1
2
24.3
17

Study Details

Study Description

Brief Summary

Urine cytology can be collected with spontaneous urine or by washing the bladder. It is commonly accepted among urologist that instrumental bladder washing is the method of choice. There are, however, no solid recommendations regarding the method to collect the urine for bladder wash cytology during cystoscopy. There are mainly two possibilities: 1) the use of an intermittent bladder catheter after the removal of the cystoscope or 2) bladder lavage through working channel of the flexible cystoscope itself. The first choice may increase the number of collected cells because of the larger caliber of the catheter compared to the working channel and thus the better efficacy of bladder wash. However, this method is certainly more invasive and possibly more expensive. To the best of our knowledge and according to available literature, none of both collection method can be defined as gold standard. The aim of the study is to show that use of flexible cystoscope brings the same results in terms of quality of the urine collection for analysis as the use of intermittent bladder catheter and is less unpleasant for the patient. If our study confirms the non-inferiority of "direct" collection through the cystoscope, this will allow the establishment of recommendations in this sense in order to simplify the procedure and reduce as much as possible the manipulations within the urogenital tract.

Condition or Disease Intervention/Treatment Phase
  • Device: Flexible cystoscopy
  • Device: Urinary catheter
N/A

Detailed Description

The aim of the study is to show that use of flexible cystoscope brings the same results in terms of quality of the urine collection for analysis as the use of intermittent bladder catheter and is less unpleasant for the patient.

Group A: Urinary cytology will be collected using a Ch.14 bladder catheter after the removal of the cystoscope. Catheter will be placed at the bladder neck level.

Group B: Urinary cytology will be collected through the flexible cystoscope itself at the end the cystoscopy. Before starting the urinary collection, the cystoscope will either be placed in front of a suspected intravesical lesion (if present) or at the bladder neck (if no lesion present).

Study Design

Study Type:
Interventional
Anticipated Enrollment :
414 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Bladder Washing Cytology for Detection of Urothelial Carcinoma Using Catheter or Flexible Cystoscope: Which is Better? A Prospective Randomized Study
Actual Study Start Date :
Nov 20, 2022
Anticipated Primary Completion Date :
Dec 1, 2023
Anticipated Study Completion Date :
Nov 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: urinary catheter

Urinary cytology will be collected using a Ch.14 bladder catheter after the removal of the cystoscope. Catheter will be placed at the bladder neck level.

Device: Urinary catheter
Urinary cytology will be collected through a Ch14 urinary catheter after the cystoscopy

Active Comparator: flexible cystoscope

Urinary cytology will be collected through the flexible cystoscope itself at the end the cystoscopy. Before starting the urinary collection, the cystoscope will either be placed in front of a suspected intravesical lesion (if present) or at the bladder neck (if no lesion present).

Device: Flexible cystoscopy
Urinary cytology will be collected through the flexible cystoscope itself at the end the cystoscopy. Before starting the urinary collection, the cystoscope will either be placed in front of a suspected intravesical lesion (if present) or at the bladder neck (if no lesion present).

Outcome Measures

Primary Outcome Measures

  1. The quality of urinary cytology according to the tool used for collection of both groups [2 years]

    Number of urothelial cells, number of inflammatory cells, presence of necrosis or blood will be used to assess this outcome measure

Secondary Outcome Measures

  1. The sensitivity and sensibility of the urinary cytology of both groups [2 years]

    Sensitivity ans specificity percentage will be calculated based on the results of both urinary cytology and cystoscopy

  2. The satisfaction of patients of both groups [2 years]

    The Faces Pain Scale will be used for each patient after the cytology to assess his satisfaction/pain (0= no pain and 10=the worst pain possible)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Men aged > or = 18 years

  2. Patients scheduled for a flexible cystoscopy and urinary cytology.

  3. Patients who have signed the informed consent.

  4. Patients who speak French

Exclusion Criteria:
  1. Manipulations or instrumentation of urinary tract, including but not limited to Double-J stent placement or removal, and/or bladder biopsy

  2. Inability to give informed consent or without capacity of discernment

Contacts and Locations

Locations

Site City State Country Postal Code
1 Centre Hospitalier Universitaire Vaudois, CHUV Lausanne VD Switzerland 1011

Sponsors and Collaborators

  • Centre Hospitalier Universitaire Vaudois

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ilaria Lucca, Principal investigator, MD, Centre Hospitalier Universitaire Vaudois
ClinicalTrials.gov Identifier:
NCT05643807
Other Study ID Numbers:
  • 2021-01124
First Posted:
Dec 9, 2022
Last Update Posted:
Dec 9, 2022
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ilaria Lucca, Principal investigator, MD, Centre Hospitalier Universitaire Vaudois
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 9, 2022