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A Novel Augmented Reality System (ARssist) for the Assistant Surgeon in Robotic Assisted Surgery

Primary Purpose

Prostate Cancer

Status
Not yet recruiting
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
ARssist system
Sponsored by
Chinese University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer focused on measuring Prostate cancer, Augmented reality, ARssist system

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 18 years old with informed consent
  • Suitable for minimally invasive surgery
  • Clinically diagnosed with urological conditions that are indicated for robotic assisted radical prostatectomy with or without lymph node dissection

Exclusion Criteria:

  • Body mass index ≥ 35 kg/m2
  • Contraindication to general anaesthesia
  • Severe concomitant illness that drastically shortens life expectancy or increases risk of therapeutic intervention
  • Untreated active infection
  • Uncorrectable coagulopathy
  • Presence of another malignancy or distant metastasis
  • Emergency surgery

Sites / Locations

  • Prince of Wales Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

ARssist system

Arm Description

The surgery will follow the same steps of a standard robotic assisted radical prostatectomy procedure, with the addition of the ARssist system used by the patient side surgeon.

Outcomes

Primary Outcome Measures

30-day complications
Complications which occur within 30 days after the operation

Secondary Outcome Measures

Performance parameters
Performance of the patient side surgeon will be assessed using Global Operative Assessment of Laparoscopic Skills (GOALS) by different evaluators, including the patient side surgeon him/herself (self-evaluation), the console surgeon, and a third-party evaluator
Performance parameters
The surgeries will be recorded audio-visually, with the captured video clips later reviewed by an independent assessor to determine objective performance outcomes of included tasks via motion analysis parameters
User-generated usability feedbacks
Specific feedback on the use of ARssist system will be collected from the patient side surgeon at the pre-operative and post-operative time points using a customized questionnaire of 10 items on a 5-point Likert scale
Operating time
Duration of operation
Blood loss
Volume of blood loss during operation
Length of hospital stay
Patients undergoing robotic radical prostatectomy have an average hospital stay of three days

Full Information

First Posted
March 9, 2020
Last Updated
June 24, 2022
Sponsor
Chinese University of Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT04304079
Brief Title
A Novel Augmented Reality System (ARssist) for the Assistant Surgeon in Robotic Assisted Surgery
Official Title
A Novel Augmented Reality System (ARssist) for the Assistant Surgeon in Robotic Assisted Surgery: A Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
March 1, 2023 (Anticipated)
Primary Completion Date
February 28, 2024 (Anticipated)
Study Completion Date
May 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Robotic prostatectomy is a surgery for treating localized prostate cancer. The ARssist system is a novel augmented reality system designed for the assistant surgeon, allowing delivery of augmented reality information via Microsoft HoloLens 2 (a head mount display developed by Microsoft) to better delineate the 3-D operative environment and enable better visualization. To date, there is no prospective study on the clinical performance and utilization of the ARssist system. This study is to evaluate the clinical feasibility and safety of the ARssist system during robotic surgery with the da Vinci Xi system.
Detailed Description
The da Vinci robotic surgery system offers advantages such as immersive three-dimensional visualization, intuitive control, and high degree of movement freedom to the chief surgeon. However, major surgery remains a team-based effort. Apart from the chief surgeon who remotely controls the da Vinci system at the console, the success of robotic assisted surgical procedures also relies on the assistant surgeon positioned at the patient side, who provides assistance laparoscopically. Throughout a robotic assisted operation, the patient side surgeon is responsible for tasks such as the exchange of instruments, retraction of tissue to enhance operative fields, manipulation of instruments, etc. Literature has demonstrated that the performance of the assistant surgeon has an effect on the outcomes of robotic surgery such as operative time. Traditionally the patient side surgeon relies on the monitor mounted on the vision cart to guide his/her movement. The monitor provides real-time relay of the image captured from the endoscope, but does not provide the full three-dimensional stereo endoscopy view unless set up with specialized stereo-vision equipment. The position of the monitor is also often awkward, creating problems such as obstructed views and non-ergonomic positioning of the patient side surgeon to overcome the view obstruction. The complex three-dimensional set-up of endoscope, robotic instruments, and hand-held instruments inside the patient body could prove difficult to imagine from the patient side surgeon's perspective, and guesswork could be involved during transfer of instruments/objects towards the operative field as the hand-held instruments are often out of the visualized field of the endoscope. Augmented reality (AR) technology delivered via optical see-through head-mounted display (OST-HMD) could potentially be the solution to the aforementioned issues. OST-HMD, such as Microsoft HoloLens, can superimpose computer graphics on top of real-world view through optical combiners. The clinical application of such a technology has been gaining interest in the surgical community, with preliminary study demonstrating feasibility of AR technology in ureteroscopic procedures. The ARssist system is a novel AR system designed for the patient side surgeon in robotic assisted surgeries. It integrates the da Vinci surgical system and Microsoft HoloLens, and provides valuable AR information to the patient side surgeon including (i) three-dimensional real-time rendering of the endoscope, robotic instruments, and hand-held instruments within the patient body, and (ii) real-time stereo endoscopy that is configurable for the assistant surgeon's preferred hand-eye coordination. The ARssist system would in theory grant the patient side surgeon improved orientation and navigation of hand-held laparoscopic instruments, thus improving their laparoscopic performance and the performance of the surgery as a whole. Based on the Innovation, Development, Exploration, Assessment, Long-term Study (IDEAL) Collaboration group methodology of promoting surgical innovation and research through planned prospective studies within an established staged process, we propose a stage 1 (Innovation) study to evaluate the feasibility and safety of the ARssist system.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Prostate cancer, Augmented reality, ARssist system

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
This is a prospective case series to be conducted as a pilot study to evaluate the clinical feasibility and safety of the ARssist system during robotic surgery with the da Vinci Xi system.
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
ARssist system
Arm Type
Experimental
Arm Description
The surgery will follow the same steps of a standard robotic assisted radical prostatectomy procedure, with the addition of the ARssist system used by the patient side surgeon.
Intervention Type
Device
Intervention Name(s)
ARssist system
Intervention Description
As stated in ARssist system arm description
Primary Outcome Measure Information:
Title
30-day complications
Description
Complications which occur within 30 days after the operation
Time Frame
Thirty days after the allocated treatment
Secondary Outcome Measure Information:
Title
Performance parameters
Description
Performance of the patient side surgeon will be assessed using Global Operative Assessment of Laparoscopic Skills (GOALS) by different evaluators, including the patient side surgeon him/herself (self-evaluation), the console surgeon, and a third-party evaluator
Time Frame
Immediately post-operative
Title
Performance parameters
Description
The surgeries will be recorded audio-visually, with the captured video clips later reviewed by an independent assessor to determine objective performance outcomes of included tasks via motion analysis parameters
Time Frame
Immediately post-operative
Title
User-generated usability feedbacks
Description
Specific feedback on the use of ARssist system will be collected from the patient side surgeon at the pre-operative and post-operative time points using a customized questionnaire of 10 items on a 5-point Likert scale
Time Frame
Immediately post-operative
Title
Operating time
Description
Duration of operation
Time Frame
Immediately post-operative
Title
Blood loss
Description
Volume of blood loss during operation
Time Frame
Immediately post-operative
Title
Length of hospital stay
Description
Patients undergoing robotic radical prostatectomy have an average hospital stay of three days
Time Frame
Three days after the allocated treatment

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 years old with informed consent Suitable for minimally invasive surgery Clinically diagnosed with urological conditions that are indicated for robotic assisted radical prostatectomy with or without lymph node dissection Exclusion Criteria: Body mass index ≥ 35 kg/m2 Contraindication to general anaesthesia Severe concomitant illness that drastically shortens life expectancy or increases risk of therapeutic intervention Untreated active infection Uncorrectable coagulopathy Presence of another malignancy or distant metastasis Emergency surgery
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jeremy Yuen Chun TEOH, MBBS, FRCSEd
Phone
+852 35052625
Email
jeremyteoh@surgery.cuhk.edu.hk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeremy Yuen Chun TEOH, MBBS, FRCSEd
Organizational Affiliation
Chinese University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Prince of Wales Hospital
City
Hong Kong
Country
Hong Kong
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jeremy Yuen Chun TEOH, MBBS, FRCSEd
Phone
35052625
Email
jeremyteoh@surgery.cuhk.edu.hk
First Name & Middle Initial & Last Name & Degree
Chi Ho LEUNG
Phone
35051663
Email
stevenleung@surgery.cuhk.edu.hk
First Name & Middle Initial & Last Name & Degree
Qinyang LIU
First Name & Middle Initial & Last Name & Degree
Chi Hang YEE
First Name & Middle Initial & Last Name & Degree
Peter Ka Fung CHIU
First Name & Middle Initial & Last Name & Degree
Samson Yun Sang CHAN
First Name & Middle Initial & Last Name & Degree
Chi Fai NG

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
27555678
Citation
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Results Reference
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Citation
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Results Reference
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A Novel Augmented Reality System (ARssist) for the Assistant Surgeon in Robotic Assisted Surgery

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