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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04551820
Other study ID # ISI-AHC-2020
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 5, 2020
Est. completion date September 30, 2021

Study information

Verified date November 2021
Source Intuitive Surgical
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

A multi-center retrospective chart review of short-term outcomes associated with robotic-assisted cholecystectomies performed during regular hours and after-hours.


Description:

The study is a retrospective multi-center chart review study of short-term patient outcomes through 30 days after robotic-assisted cholecystectomies performed during regular hours and after-hours. The primary outcomes include the rate of conversion to open, rate of intra-operative adverse events, the rate of post-operative adverse events relating to the cholecystectomy within 30 days, and re-admissions and re-operations relating to the cholecystectomy within 30 days. In addition, operative time, the rate of use of intra-operative imaging, and the hospital length of stay will be collected as secondary outcomes.


Recruitment information / eligibility

Status Completed
Enrollment 520
Est. completion date September 30, 2021
Est. primary completion date September 30, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Subject between 18 and 80 years of age at the time of surgery. - Subject underwent a robotic-assisted cholecystectomy during the study time period. Exclusion Criteria: - Cholecystectomy was performed as a secondary procedure.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Regular Hours
The regular hours cohort includes cholecystectomies performed during the day shift at the Institution during Monday through Friday, not inclusive of national holidays.
After Hours
The after hours cohort includes cholecystectomies performed outside of the day shift at the Institution during Monday through Friday, on the weekend, or during a national holiday.
Device:
Robotic-assisted Cholecystectomy
With the patient under general anesthesia, several small incisions are made in the abdomen. Ports are placed, the abdomen is insufflated, and the da Vinci Robotic Surgical System (Intuitive) is docked to the patient and used to complete the cholecystectomy according to the surgeon's standard of care.

Locations

Country Name City State
United States St. David's Medical Center Austin Texas

Sponsors (1)

Lead Sponsor Collaborator
Intuitive Surgical

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Conversion to open The rate of conversion of the cholecystectomy to open, defined as robotic-assisted surgery converted to an open approach. Intra-operative
Primary Number of adverse events Intra-operative or post-operative adverse events related to the cholecystectomy Intra-operative through the 30 day follow-up period
Primary Re-admissions Re-admissions to the hospital related to the cholecystectomy through the 30 day follow-up period After discharge from the hospital post-procedure through the 30 day follow-up period
Primary Re-operations Re-operations related to the cholecystectomy through the 30 day follow-up period After the procedure but prior to discharge, through the 30 day follow-up period
Secondary Operative time Operative time, defined as first incision to closure of the incision Intra-operative
Secondary Use of intra-operative imaging The rate of use of intra-operative imaging, including indocyanine green fluorescent imaging and cholangiography Intra-operative
Secondary Length of Hospital Stay (LOS) How long the patient was admitted to the hospital From admission to discharge, up to approximately one week
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