Office-Based Ureteroscopy Utilizing a Single Use Digital, Flexible Ureteroscope for Upper Tract Urothelial Carcinoma

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Michigan Rogel Cancer Center

About this trial

This clinical trial tests how well office based ureteroscopy utilizing a single use digital, flexible ureteroscope works for the assessment of upper tract urothelial carcinoma. Ureteroscopy is a procedure in which a thin camera called a ureteroscope is used to assess patients with a known or suspected diagnosis of upper tract urothelial carcinoma. Ureteroscopy is traditionally performed in an operating room under general anesthesia. In this study, patients undergo ureteroscopy in the doctor's office using an ultra-thin ureteroscope, which is the narrowest instrument of its kind. Because of its small size, researchers believe this procedure can be completed in the office with minimal discomfort and high patient satisfaction, which may eliminate the risks of general anesthesia and reduce delays to diagnosis. Office based ureteroscopy utilizing a single use digital, flexible ureteroscope may be effective for the assessment of upper tract urothelial carcinoma.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Provision of signed and dated informed consent form

Stated willingness to comply with all study procedures and availability for the duration of the study

Male or female, aged ≥ 18 year. Both sexes are included to reflect the patient population with upper tract urothelial carcinoma (UTUC) already being followed at the University of Michigan and allow exploration of potential differences in tolerability of awake ureteroscopy based on sex

History of endoscopically managed UTUC at any time, or a suspected diagnosis of UTUC based on pre-procedure imaging, and is already planned for office-based ureteroscopic assessment

Disqualifiers

Known ureteral strictures

Active urinary tract infection

Need for general anesthesia due to patient or procedural factors

History of inability to tolerate ureteroscopy under local anesthetic

Trial design

Design model

Single group

Treatments tested in this trial

  • Analgesic Agent

    Drug

    Given PO

  • Electronic Health Record Review

    Other intervention

    Ancillary studies

  • Lidocaine Topical

    Drug

    Given intraurethrally

  • Medical Device Usage and Evaluation

    Device

    Undergo ureteroscopy using 6.3 Fr single use digital ureteroscope

  • Survey Administration

    Other intervention

    Ancillary studies

  • Ureteroscopy

    Procedure/Surgery

    Undergo ureteroscopy

Treatment groups

10 Participants
are divided into 1 treatment group
Group A: Diagnostic (in office ureteroscopy)Experimental treatment 6 interventions

Trial outcomes

Primary outcomes

1

Success rate

Defined as the ability to successfully perform and complete upper and lower tract surveillance with the 6.3 French ureteroscope in an office setting. A study-wide successful outcome will be defined as a success rate of 70%. The success rate will be reported as the count and proportion of participants with a successful outcome out of the number of enrolled participants. The corresponding 95% binomial Clopper-Pearson confidence interval will be reported.

Time frame
On day of procedure

Secondary outcomes

1

Pain

Assessed by intra- and peri-procedure patient reported outcomes with the visual analogue scale pain score, as well as the Patient-Reported Outcomes Measurement Information System Pain Interference and Intensity score. Will be summarized and displayed graphically with means, standard deviations and/or quartiles.

Time frame
From baseline up to 7-10 days post procedure
2

Satisfaction

Assessed by the International Consultation on Incontinence-Satisfaction. Will be summarized and displayed graphically with means, standard deviations and/or quartiles.

Time frame
At 7-10 days post procedure
3

Unplanned healthcare use

Will measure unplanned healthcare utilization including electronic messages, phone calls, lab and imaging tests, emergency department visits, hospitalizations, and secondary interventions. These will be reported as counts of events and counts of participants with corresponding proportions of enrolled participants.

Time frame
From baseline up to 30 days post procedure

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Michigan Rogel Cancer Center

Lead sponsor

Shenzhen HugeMed Medical Technical Development

Collaborator