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

Phase II Study of the Da Vinci Single Port (SP) Robotic System for Abdominal and Pelvic Procedures

Who can join

Ages 18 and older · All sexes

Inclusion Criteria:

* 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

Exclusion Criteria:

* 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

About the study

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.

What is being tested

• Robot-Assisted Surgery (device)

Sponsor: City of Hope Medical Center · Participants: 33 · Started: Apr 26, 2024

Contact the study team

Official record on ClinicalTrials.gov — NCT05672368

Locations in the U.S.

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.