Reducing unnecessary preoperative testing for low-risk surgeries
Official title: De-Implementation of Low-value Testing in Patients Undergoing Low-Risk Surgery
Run by University of Michigan · NCT06934564 · Data updated 2026-11-12
This study is testing a new approach to see if we can cut down on unnecessary medical tests before low-risk surgeries to make things easier and better for patients.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 16 (estimated) |
| Sponsor | University of Michigan Academic / other |
| Locations | 1 site (Ann Arbor, Michigan) |
| Status | Recruiting |
| Started | April 1, 2025 |
| Main results expected | December 2026 |
| Study ends | December 2026 |
| Registry record updated | May 8, 2026 |
| Trial ID | NCT06934564 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are patients undergoing low-risk surgeries with a history of high preoperative testing rates.
✕Probably not a fit
Patients who are not undergoing the specified low-risk surgeries may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This trial evaluates a multi-level strategy to decrease low-value preoperative testing in patients undergoing low-risk surgeries such as breast lumpectomy, laparoscopic cholecystectomy, and inguinal hernia repair. Sixteen sites in Michigan will implement proven tools including clinician education, decision aids, performance audits, and pay-for-performance incentives. The goal is to significantly reduce unnecessary testing through these interventions, ultimately improving patient care and resource utilization.
Why it matters
Potential benefit: If successful, this approach could lead to more efficient surgical care and reduced healthcare costs for patients.
How similar studies have gone: Other studies have shown success in reducing unnecessary testing through similar de-implementation strategies, indicating a promising approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Site Inclusion Criteria: * Over 30% of testing rates on at least one of the three index procedures (breast lumpectomy, laparoscopic cholecystectomy, and inguinal hernia repair) Exclusion Criteria: * none Surgical participants must be over 18 years old.
Where it's running
-
University of Michigan and other Michigan Surgical Quality Collaborative sites
Ann Arbor, Michigan, United States Recruiting
Study contacts
- Principal investigator: Lesly Dossett, MD, MPH — University of Michigan
- Study coordinator: Dana Greene Jr., MPH
- Email: greenejr@med.umich.edu
- Phone: (313)-670-0408
Similar studies
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.