Reducing unnecessary preoperative testing for low-risk surgeries
De-Implementation of Low-value Testing in Patients Undergoing Low-Risk Surgery
NA · University of Michigan · NCT06934564
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
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 16 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Michigan (other) |
| Locations | 1 site (Ann Arbor, Michigan) |
| Trial ID | NCT06934564 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates are patients undergoing low-risk surgeries with a history of high preoperative testing rates.
Not a fit: Patients who are not undergoing the specified low-risk surgeries may not benefit from this study.
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 performed: Other studies have shown success in reducing unnecessary testing through similar de-implementation strategies, indicating a promising approach.
Eligibility criteria
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 this trial is running
Ann Arbor, Michigan
- 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
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Breast Lumpectomy, Laparoscopic Cholecystectomy, Inguinal Hernia Repair, Preoperative testing