Actively Recruiting
The da Vinci Single Port Robotic System for Use in Abdominal and Pelvic Surgical Procedures
Led by City of Hope Medical Center · Updated on 2026-04-20
33
Participants Needed
1
Research Sites
128 weeks
Total Duration
On this page
Sponsors
C
City of Hope Medical Center
Lead Sponsor
N
National Cancer Institute (NCI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This phase II trial test the effectiveness and safety of a single-port robotic device (the da Vinci single port \[SP\]1098) for use in abdominal and pelvic surgeries. The da Vinci SP1098 robotic device can be used to perform less invasive surgeries that allow entry into the body through a single, small incision. The use of this device during surgery may allow surgeons to perform complex procedures that result in less pain, fewer complications and side effects, and improved recovery.
CONDITIONS
Official Title
The da Vinci Single Port Robotic System for Use in Abdominal and Pelvic Surgical Procedures
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Documented informed consent of the participant and/or legally authorized representative
- Any patient scheduled to undergo robot-assisted abdominal or pelvic procedures
- Age over 18 years
You will not qualify if you...
- Body mass index (BMI) over 45
- Contraindications to minimally invasive surgery including chronic obstructive pulmonary disorders
- Past history of failed attempt of minimally invasive abdominal or pelvic surgery
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
City of Hope Comprehensive Cancer Center
Duarte, California, United States, 91010
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DEVICE_FEASIBILITY
Number of Arms
1
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