Comparing robotic-assisted and laparoscopic appendectomies for acute appendicitis
A Retrospective Multicenter Evaluation of Short-Term Outcomes After Acute Care Appendectomy
Intuitive Surgical · NCT06624215
This study looks at how well robotic-assisted surgery compares to traditional laparoscopic surgery for treating acute appendicitis to see which method might be better for patients.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1000 (estimated) |
| Ages | 22 Years and up |
| Sex | All |
| Sponsor | Intuitive Surgical (industry) |
| Locations | 3 sites (Columbus, Ohio and 2 other locations) |
| Trial ID | NCT06624215 on ClinicalTrials.gov |
What this trial studies
This observational study aims to analyze perioperative data from patients who underwent either robotic-assisted or laparoscopic appendectomy for acute appendicitis. By reviewing cases from 2018 to 30 days prior to IRB approval, the study seeks to identify differences in outcomes between the two surgical approaches. The focus is on emergent or urgent procedures, providing insights into their effectiveness and safety. The findings could help inform surgical practices and patient care in acute appendicitis cases.
Who should consider this trial
Good fit: Ideal candidates are adults aged 22 and older who have had an emergent or urgent robotic-assisted or laparoscopic appendectomy for acute appendicitis.
Not a fit: Patients with appendiceal neoplasms, those who underwent single-port appendectomy, or who were pregnant or breastfeeding at the time of the procedure may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance surgical decision-making and improve patient outcomes for those undergoing appendectomy.
How similar studies have performed: Previous studies have shown promising results in comparing robotic-assisted and laparoscopic techniques, indicating that this approach is supported by existing research.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Columbus, Ohio and 2 other locations
- The Ohio State University — Columbus, Ohio, United States (RECRUITING)
- Legacy Emanuel Hospital & Health Center — Portland, Oregon, United States (RECRUITING)
- Christus Santa Rosa Health Care Corporation — New Braunfels, Texas, United States (RECRUITING)
Study contacts
- Study coordinator: Auben Debus, Sr. Clinical Study Manager
- Email: auben.debus@intusurg.com
- Phone: 408-523-5294
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: Acute Appendicitis, Appendectomy, Robotic-assisted, Acute care, Laparoscopic