RECRUITING Phase 2 ClinicalTrials.gov

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

Sponsor: City of Hope Medical Center • ClinicalTrials.gov ID: NCT05672368

Registry updated: 2026-10-08

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Description

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.

Interventions

Robot-Assisted Surgery (Device)
Undergo surgery using the da Vinci SP device

Eligibility criteria

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

Conditions

Disease or Disorder

Locations

City of Hope Comprehensive Cancer Center — Duarte, California, United States

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Official Source

Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

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