Disposable scope takes on stent removal – does it stack up?
NCT ID NCT04829461
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a single-use, disposable cystoscope (aScope™ 4 Cysto) for removing ureteral stents, comparing it to standard reusable scopes. 102 adults with stents ready for removal took part. The main goal was to see if the disposable scope could successfully remove stents as well as the usual reusable ones.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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102 people
The number who actually took part.
- Started
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Apr 2021
- Finished
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Jul 2022
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Adult (male or female), ≥18 years old 2. Patient undergoing routine flexible cystoscopy 3. Patient with a ureteral stent in the urinary system that is ready to be removed. 4. No active urinary tract infection 5. Subject is willing and able to sign informed consent and HIPAA authorization and comply with requirements of the protocol. Exclusion Criteria: 1. History of prior bladder/urethral reconstructive surgery. 2. History of high-grade bladder cancer or carcinoma in-situ of the bladder, undergoing cystoscopy for follow-up/surveillance purposes. 3. Known unpassable urethral stricture 4. Febrile patient with active urinary tract infection (UTI) 5. Subjects with acute infection (acute urethritis, acute prostatitis, acute epididymitis) 6. Subject with severe coagulopathy 7. Patient is unable to read and/or understand study requirements 8. Patient is unable or unwilling to provide written consent to participate in the study. 9. Subject, in the opinion of the Investigator, has a severe comorbidity, poor general physical/mental health and/or a condition that will not
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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The Pennsylvania State University and The Milton S. Hershey Medical Center
Hershey, Pennsylvania, 17033, United States
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University of Texas Southwestern Medical Center
Dallas, Texas, 75390, United States
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University of Wisconsin-Madison
Madison, Wisconsin, 53792, United States
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