SPARC: Study of Peri-operative and Acute Outcomes After Robotic-assisted Cholecystectomy

Sponsor
Intuitive Surgical (Industry)
Overall Status
Completed
CT.gov ID
NCT04551820
Collaborator
(none)
520
1
13.8
37.6

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Procedure: Regular Hours
  • Procedure: After Hours
  • Device: Robotic-assisted Cholecystectomy

Detailed 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.

Study Design

Study Type:
Observational
Actual Enrollment :
520 participants
Observational Model:
Case-Only
Time Perspective:
Retrospective
Official Title:
SPARC: Study of Peri-operative and Acute Outcomes After Robotic-assisted Cholecystectomy
Actual Study Start Date :
Aug 5, 2020
Actual Primary Completion Date :
Sep 30, 2021
Actual Study Completion Date :
Sep 30, 2021

Arms and Interventions

Arm Intervention/Treatment
Regular Hours

These subjects have undergone a cholecystectomy during regular hours at the Institution.

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.

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.

After Hours

These subjects have undergone a cholecystectomy during after hours at the Institution.

Procedure: 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.

Outcome Measures

Primary Outcome Measures

  1. Conversion to open [Intra-operative]

    The rate of conversion of the cholecystectomy to open, defined as robotic-assisted surgery converted to an open approach.

  2. Number of adverse events [Intra-operative through the 30 day follow-up period]

    Intra-operative or post-operative adverse events related to the cholecystectomy

  3. Re-admissions [After discharge from the hospital post-procedure through the 30 day follow-up period]

    Re-admissions to the hospital related to the cholecystectomy through the 30 day follow-up period

  4. Re-operations [After the procedure but prior to discharge, through the 30 day follow-up period]

    Re-operations related to the cholecystectomy through the 30 day follow-up period

Secondary Outcome Measures

  1. Operative time [Intra-operative]

    Operative time, defined as first incision to closure of the incision

  2. Use of intra-operative imaging [Intra-operative]

    The rate of use of intra-operative imaging, including indocyanine green fluorescent imaging and cholangiography

  3. Length of Hospital Stay (LOS) [From admission to discharge, up to approximately one week]

    How long the patient was admitted to the hospital

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 St. David's Medical Center Austin Texas United States 78758

Sponsors and Collaborators

  • Intuitive Surgical

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Intuitive Surgical
ClinicalTrials.gov Identifier:
NCT04551820
Other Study ID Numbers:
  • ISI-AHC-2020
First Posted:
Sep 16, 2020
Last Update Posted:
Nov 26, 2021
Last Verified:
Nov 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Product Manufactured in and Exported from the U.S.:
Yes

Study Results

No Results Posted as of Nov 26, 2021