Tests robotic surgery system in children and young people for several operations
Tests the da Vinci Xi robotic system in children and teens for surgery.
Plain-language title generated from the registry record
Registry title: Stanford Program to Accelerate Robotic Children's Surgery
Key facts
- Where
- Stanford, United StatesSee the site
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 6 and 21 years old?
Source: NCT06671639, who can take part
Where in United States
- Lucile Packard Children's Hospital StanfordStanford, United StatesTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Stanford University
- Trial code
- NCT06671639
- Record updated
- 30 April 2026
- Original description
The goal of this clinical trial is to provide additional data to confirm safety and performance of the da Vinci Xi Surgical System in a human clinical setting. This pilot study is intended to provide an initial assessment to evaluate the feasibility, safety, and effectiveness for the utilization of the da Vinci Xi on pediatric and adolescent patients. This clinical trial will be conducted under the auspices of Stanford University's IRB approval.Read full original descriptionShow less
Stanford Program to Accelerate Robotic Children's Surgery
The goal of this clinical trial is to provide additional data to confirm safety and performance of the da Vinci Xi Surgical System in a human clinical setting. This pilot study is intended to provide an initial assessment to evaluate the feasibility, safety, and effectiveness for the utilization of the da Vinci Xi on pediatric and adolescent patients. This clinical trial will be conducted under the auspices of Stanford University's IRB approval.
Inclusion: Subject is between 6 - 21 years of age (weighing at least 15 kilograms); Subject clinically diagnosed with a medical condition for which one of the study procedures is appropriate therapy and selected as the treatment of choice by the guardian and surgeon; Subject without previous treatment using a robotic surgery device; Subject or their guardian is willing and able to provide written informed consent; Subject or their guardian is willing and able to comply with the study protocol requirements.
Exclusion: Subject is contraindicated for general anesthesia or surgery; Subject is mentally handicapped or has a psychological disorder or severe systemic illness that would preclude compliance with study requirements or ability to provide informed consent; Subject with uncorrected coagulopathy; Subject has clinical requirement for primary open operative procedure; Subject is ASA 4 or 5 status; Subject is pregnant or suspected to be pregnant.