Exploring the Potential of Robotic Telesurgery in Remote Settings

AdventHealth

Status

Enrolling

Conditions

Prostate Disease

Prostate Carcinoma

Treatments

Device: Telesurgery utilizing Microport Medbot Robotic Platform

Study type

Interventional

Funder types

Other

Identifiers

NCT07130708

2294288

Details and patient eligibility

About

This study involves a type of robotic surgery called telesurgery, where a highly trained surgeon performs the surgical procedure using a secure internet connection to operate on a patient in a different location. Urologists from The goal of this study is to find out how safe and effective telesurgery is when used in real hospitals. The study aims to understand how well Telesurgery works in different settings, what technical challenges might come up (like internet speed or delays), and how it can be used to train new surgeons.

Enrollment

10 estimated patients

Sex

Male

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age 18 - 90
Male or female
Eligible participants for this telesurgery study must have a clearly defined indication for robotic urologic surgery, specifically:
- Localized Prostate Cancer (ICD-10: C61), appropriate for robotic radical prostatectomy.

-Benign Prostate diseases appropriate for robotic simple prostatectomy (ICD-10: N40) These diagnoses are confirmed by clinical examination, imaging, and/or pathology prior to surgical planning. Patients with vague or unspecified urologic conditions will be excluded to ensure the safety and appropriateness of the surgical intervention.

Primary diagnosis of urinary system disease and prostate disorders (C61 and N40.1) scheduled to undergo treatment with robotic surgery. These patients don't have access to robotic surgery in their routine and the study will give them the opportunity to have advanced technology and the gold-standard treatment with experts in the field.
Willing to participate in the study
Mentally capable of comprehending the study protocol

Exclusion criteria

Patients who, based on multidisciplinary evaluation (surgical, anesthetic, and medical), are deemed not suitable for robotic surgery due to high perioperative risk. This includes but is not limited to:
- Uncontrolled cardiovascular, pulmonary, or metabolic disease.
- Severe anesthetic risk classified as ASA Class IV or higher.
Patients enrolled in another interventional research study that may interfere with surgical safety or outcomes.
Patients unwilling or unable to comply with the perioperative and follow-up schedule.
Vulnerable populations are excluded from this study, including:
- Minors (under 18 years old)
- Prisoners
- Cognitively impaired or decisional incapacitated individuals