The da Vinci Single Port Robotic System for Use in Abdominal and Pelvic Surgical Procedures

Recruiting now · Phase 2

Conditions studied: Disease or Disorder

In brief

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.

Key facts

Study ID

NCT05672368

Run by

City of Hope Medical Center

People needed

33

Starts

2024-04-26

Expected to finish

2026-10-13

Last updated by the study team

2026-04-20

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Documented informed consent of the participant and/or legally authorized representative
• Any patient scheduled to undergo robot-assisted abdominal or pelvic procedures
• Age > 18 years

You may not qualify if…

• Body mass index (BMI) > 45
• Contraindications to minimally invasive surgery including chronic obstructive pulmonary disorders
• Past history of failed attempt of minimally invasive abdominal or pelvic surgery

Where it is running

• City of Hope Comprehensive Cancer Center — Duarte, California, United States (enrolling)

Full record on ClinicalTrials.gov

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