AI Visualization for Robotic Urologic Surgery

Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: University of Illinois at Chicago
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to assess the impact of using AI (artificial intelligence) during robotic urologic surgeries on surgeons and their assistants. The study evaluates whether AI tools that provide real-time visuals affect the ease or difficulty of surgery by measuring the mental effort of the surgical team. Participants are divided into three groups: one with continuous AI visuals, one without AI visuals, and one with AI visuals used only at key times. The trial primarily targets urology surgeons and residents involved in these surgeries. As an unphased trial, it offers participants the opportunity to contribute to groundbreaking research that could enhance surgical precision and outcomes.

Will I have to stop taking my current medications?

The trial information does not specify whether participants need to stop taking their current medications.

What prior data suggests that AI visualization for robotic urologic surgery is safe?

Past studies have examined the use of artificial intelligence (AI) in robotic urologic surgery for its potential to enhance precision and safety. Research has shown that AI can assist surgeons by providing real-time guidance and identifying critical structures, such as blood vessels and nerves, during surgery. This assistance helps prevent accidental harm to these vital areas, making surgeries safer.

No major reports have indicated problems directly caused by the AI technology itself. The technology primarily aids the surgical process without altering it in a harmful way. It has demonstrated effectiveness in the surgical setting.

For those considering participation in clinical trials involving AI technology, it is reassuring that this technology has been used in similar contexts without major safety concerns. While ongoing research aims to improve and further understand these tools, current evidence supports their safe use in robotic surgeries.12345

Why are researchers excited about this trial?

Researchers are excited about this trial because it explores how AI visualization could enhance robotic urologic surgeries. Unlike traditional surgeries that rely solely on the surgeon’s skill and experience, this trial examines continuous and intermittent AI overlays to provide real-time guidance during operations. The continuous AI visualization offers a constant stream of data, potentially improving precision and outcomes. Meanwhile, the intermittent AI option allows surgeons to activate the overlay during crucial moments, offering flexibility and control. This innovative use of AI in surgery could lead to more accurate procedures and better patient outcomes, a big leap from current techniques.

What evidence suggests that this trial's AI visualization strategies could be effective for robotic urologic surgery?

Research has shown that artificial intelligence (AI) in robotic urologic surgery can greatly enhance the procedure. AI increases surgical precision by 40% and speeds up recovery compared to traditional methods. In this trial, participants will experience different approaches: some will have continuous AI visualization throughout the entire surgical procedure, while others will have intermittent AI visualization, activated selectively during key surgical phases. A separate group will undergo surgery without AI visualization. Studies have found that AI-assisted surgery results in less blood loss and shorter hospital stays. These advantages make AI a promising tool for better surgical outcomes.12467

Are You a Good Fit for This Trial?

This trial is for urology surgeons or urology residents who perform robotic surgeries. Only those currently practicing in these roles can participate.

Inclusion Criteria

Inclusion Criteria: Urology surgeon or urology resident -

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Surgical Procedure

Participants undergo single-port robotic surgery with varying AI visualization strategies

1 day
1 visit (in-person)

Immediate Post-Operative Assessment

Participants' cognitive workload is assessed using the NASA-TLX questionnaire

30 minutes after surgery

Follow-up

Participants are monitored for safety and effectiveness after the surgical procedure

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Yolo

Trial Overview

The study tests how using AI-based visualization tools (like Yolo overlays via the da Vinci TilePro display) during single-port robotic urologic surgery affects the mental workload of both console surgeons and bedside assistants, measured by NASA-TLX scores.

How Is the Trial Designed?

3

Treatment groups

Active Control

Group I: Continuous AI visualizationActive Control1 Intervention
Group II: No AI visualizationActive Control1 Intervention
Group III: Intermittent AI visualizationActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of Illinois at Chicago

Lead Sponsor

Trials
653
Recruited
1,574,000+

Citations

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