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Recruiting Not applicable Interventional

Stent Omission After Ureteroscopy and Lithotripsy in the Michigan Urological Surgery Improvement Collaborative

ClinicalTrials.gov ID: NCT05866081

Public ClinicalTrials.gov record NCT05866081. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 8, 2026, 2:01 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Stent Omission After Ureteroscopy and Lithotripsy in the Michigan Urological Surgery Improvement Collaborative (SOUL MUSIC)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a multicenter prospective trial with randomized and observational cohorts assessing patient-reported outcomes and unplanned healthcare utilization following ureteroscopic treatment of renal and ureteral stones, with placement versus omission of a ureteral stent. Eligible participants in the randomization trial will be randomized to ureteroscopy with stent placement or stent omission. Eligible participants that consent to the observational only cohort will complete surveys and the treating physicians will decide the treatment options for the participants. The study team hypothesizes that: * Pain interference change from pre-surgery to Day 7-10 will differ between the two treatment arms. This hypothesis will be evaluated separately in the randomized and observational cohorts. * Unplanned healthcare utilization in the treatment arms will have different unplanned healthcare utilization ranks leading to a win proportion significantly higher or lower than 0.5 in the stent omission arm compared to the stent placement arm. This hypothesis will be evaluated separately in the randomized and observational cohorts.

Study identification

NCT ID
NCT05866081
Recruitment status
Recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
University of Michigan
Other
Enrollment
792 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 31, 2023
Primary completion
Apr 30, 2026
Completion
Apr 30, 2026
Last update posted
Dec 14, 2025

2023 – 2026

United States locations

U.S. sites
16
U.S. states
6
U.S. cities
15
Facility City State ZIP Site status
University of Arizona Tucson Arizona 85724 Recruiting
UF Health Shands Hospital Gainesville Florida 32608 Recruiting
Indiana University Department of Urology Indianapolis Indiana 46202 Recruiting
University of Michigan Health System Ann Arbor Michigan 48111 Recruiting
University of Michigan Health System Brighton Michigan 48116 Recruiting
Cadillac Munson Hospital Cadillac Michigan 49601 Recruiting
St. Joseph Health System Chelsea Hospital Chelsea Michigan 48118 Recruiting
St. Joseph Mercy Health (Trinity) Chelsea Michigan 48118 Recruiting
Henry Ford Health System Detroit Michigan 48202 Recruiting
Corewell Health Buttersworth Hospital Grand Rapids Michigan 49503 Recruiting
E.W Sparrow Hospital Lansing Michigan 48912 Recruiting
MyMichigan Medical Center Midland Midland Michigan 48670 Recruiting
Michigan Institute of Urology Town Center Ambulatory Surgery Center Troy Michigan 48084 Recruiting
Monte Fiore Brooklyn New York 10467 Recruiting
Mount Sinai New York New York 10029 Recruiting
UNC Hospital Chapel Hill North Carolina 27514 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05866081, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 14, 2025 · Synced Sep 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05866081 live on ClinicalTrials.gov.

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