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Retrospective Acute Care Appendectomy Study

A Retrospective Multicenter Evaluation of Short-Term Outcomes After Acute Care Appendectomy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06624215
Enrollment
1000
Registered
2024-10-02
Start date
2024-11-22
Completion date
2026-11-01
Last updated
2026-04-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Appendicitis

Keywords

Appendectomy, Robotic-assisted, Acute care, Laparoscopic

Brief summary

The purpose of this retrospective study is to compare perioperative data for subjects who have undergone an emergent or urgent robotic-assisted or laparoscopic appendectomy for acute appendicitis.

Interventions

PROCEDUREAppendectomy

Robotic-assisted or laparoscopic appendectomy for acute appendicitis.

Sponsors

Intuitive Surgical
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
22 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Subject is 22 years of age or older at time of procedure * Subject has undergone robotic-assisted or laparoscopic emergent or urgent appendectomy for acute appendicitis between 2018 and 30 days prior to IRB approval

Exclusion criteria

* Subject with appendiceal neoplasms * Subject who underwent a single-port appendectomy * Subject who was pregnant or breastfeeding at the time of the procedure

Design outcomes

Primary

MeasureTime frameDescription
Operative timeIntraoperative
Procedure timeIntraoperative
ConversionIntraoperative
Adverse eventsIntraoperative and postoperative out to 30 days from procedure date
Mortality rate through 30 daysIntraoperative and postoperative out to 30 days from procedure dateAll cause
Unplanned procedure-related readmission rate through 30 daysDischarge through 30 days
Concomitant proceduresIntraoperative
Estimated blood lossIntraoperative
Severity of appendicitisPreoperative
Unplanned procedure-related reoperation rate through 30 daysPostoperative through 30 days
Length of stayStart of procedure to discharge from the hospital (check-out time), up to approximately one weekTotal number of days the subject stayed in the hospital after the index procedure prior to being discharged.
Discharge dispositionDischarge from the hospital (check-out time), up to approximately one week.Where the subject was discharged to when released from the hospital
Blood TransfusionIntraoperative and discharge from the hospital (check-out time), up to approximately one week.Any occurrence of blood transfusion either at the time of the procedure or at any point during the post-procedure hospitalization until the participant is discharged.

Countries

United States

Contacts

CONTACTAuben Debus, Sr. Clinical Study Manager
auben.debus@intusurg.com408-523-5294

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 23, 2026