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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03471377
Other study ID # 18-115
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 5, 2018
Est. completion date March 15, 2022

Study information

Verified date March 2022
Source Memorial Sloan Kettering Cancer Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The investigators are studying the duration it takes surgeons to complete their respective surgical cases. The hospital hopes to improve the overall operating room scheduling accuracy from this project.


Recruitment information / eligibility

Status Completed
Enrollment 683
Est. completion date March 15, 2022
Est. primary completion date March 15, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - A surgeon or OR staff member in the Department of Surgery Gynecology and Colorectal service Exclusion Criteria: - Any new surgeon that starts their practice during the study - Surgery will take place at a location other than the Main hospital or Josie Robertson Surgical Center - Cases where input data was not available prior to the prediction generation including late add-on cases such as urgent and emergent cases that are placed on the schedule less than 24 hours before the surgery

Study Design


Related Conditions & MeSH terms


Intervention

Other:
standard scheduling process
Scheduling office assigns start time and room for case and places case on schedule. At this point a default case duration is evaluated by the scheduling office, to see if the value is considered excessively short or excessively long. Depending on the assessment, the scheduling office will either keep the default value, use the value that the surgeon placed in the notes (if available), or the scheduling office provides their own estimation.
assigned a planned case duration value from predictive model
Predictive model calculates new duration for case at 3AM the day before surgery, and the predictions are made available on a SecureShare-site. Model predictions are then read by scheduling manager sometime between 7am-10am from the SecureShare site, and the scheduling manager will in EPIC/OpTime, overwrite the current estimate with the new duration value that was generated by the predictive model.

Locations

Country Name City State
United States Memoral Sloan Kettering Basking Ridge New York New York

Sponsors (1)

Lead Sponsor Collaborator
Memorial Sloan Kettering Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary duration it takes surgeons to complete their respective surgical cases All Gynecology (GYN) and Colorectal (CRS) Surgeons at MSKCC will be included. To test the hypothesis that the developed surgical case duration prediction model compared to the current process of estimating surgical case durations, will show improved prediction accuracy, measured by mean absolute error. 1 year
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