RECRUITING

Exploring the Potential of Robotic Telesurgery in Remote Settings

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Advancing Humanitarian Healthcare: Exploring the Potential of Robotic Telesurgery in Remote Settings - A Multicentric Prospective Study

Quick Facts

Study Start:2025-06-14
Study Completion:2033-07-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07130708

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 90 Years
Sexes Eligible for Study:MALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age 18 - 90
  2. * Male or female
  3. * Eligible participants for this telesurgery study must have a clearly defined indication for robotic urologic surgery, specifically:
  4. * Localized Prostate Cancer (ICD-10: C61), appropriate for robotic radical prostatectomy.
  5. * 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.
  6. * Willing to participate in the study
  7. * Mentally capable of comprehending the study protocol
  1. * 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:
  2. * Uncontrolled cardiovascular, pulmonary, or metabolic disease.
  3. * Severe anesthetic risk classified as ASA Class IV or higher.
  4. * Patients enrolled in another interventional research study that may interfere with surgical safety or outcomes.
  5. * Patients unwilling or unable to comply with the perioperative and follow-up schedule.
  6. * Vulnerable populations are excluded from this study, including:
  7. * Minors (under 18 years old)
  8. * Prisoners
  9. * Cognitively impaired or decisional incapacitated individuals

Contacts and Locations

Study Locations (Sites)

AdventHealth
Celebration, Florida, 34747
United States

Collaborators and Investigators

Sponsor: AdventHealth

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-06-14
Study Completion Date2033-07-30

Study Record Updates

Study Start Date2025-06-14
Study Completion Date2033-07-30

Terms related to this study

Keywords Provided by Researchers

  • Robotic Prostatectomy
  • Prostate Cancer
  • Telesurgery

Additional Relevant MeSH Terms

  • Prostate Carcinoma
  • Prostate Disease