Prince of Wales Hospital, The Chinese University of Hong Kong
Hong Kong, China
NCT Number: NCT03010813
This is a prospective, single center, multispecialty study that aimed to evaluate the clinical feasibility and safety of single port surgery and NOTES (mainly transanal and transoral surgery) using a novel single port robotic system.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Hong Kong, China
Background: Single port surgery and natural orifice transluminal endoscopic surgery (NOTES) are emerging minimally invasive surgery techniques which can further reduce patient trauma and enhance recovery. However, the wider adoption of these techniques is hampered by the limitation of instrumentation and technical difficulties. Robotic assistance may improve surgical capabilities during single port surgery and NOTES by providing augmented motion precision and manipulation dexterity.
Objectives: To evaluate the clinical feasibility and safety of single port surgery and NOTES (mainly transanal and transoral surgery) using a novel single port robotic system.
Design: Prospective, single center, multispecialty study consistent with a stage 1 (Innovation) study described in the Innovation, Development, Exploration, Assessment, Long-term Study (IDEAL) framework.
Subjects: Sixty consecutive patients with various benign/malignant pathologies indicated for single port colorectal/urologic surgery or transanal/transoral surgery who fulfilled all the inclusion and exclusion criteria will be recruited.
Intervention: Single port surgery and transanal/transoral surgery will be performed using the novel single port robotic system.
Study Endpoints: Primary: conversion rate and perioperative complications. Secondary: operative time, blood loss, pain scores, analgesic requirement, and length of stay.
Hypothesis: The prospective study will provide important information on the feasibility, safety, and effectiveness of the novel single port robotic system in performing single port surgery and NOTES in various surgical specialties. A positive study will provide supporting evidence for continuing development of this new technology.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
GENERAL INCLUSION CRITERIA FOR ALL PROCEDURES
GENERAL EXCLUSION CRITERIA FOR ALL PROCEDURES
Robotic single port colorectal surgery; Robotic transanal surgery; Robotic single port urologic surgery; Transoral robotic surgery
Time frame: Up to 1 month
An emergent change in the treatment plan to conventional minimally invasive (laparoscopic/endoscopic) surgery (i.e. the use of more than one additional port), multiport robotic surgery, or to open surgery
Time frame: Up to 1 month
Complications including intraoperative complications and all complications occurring during the hospital stay or within 30 days after discharge will be graded according to the Clavien-Dindo classification
Time frame: Intraoperative
Time frame: Up to 1 month
Time frame: Up to 1 month
Time frame: Up to 1 month
Time frame: Up to 1 month
Time frame: Up to 1 month
Pathologic examination of the resected specimen for completeness of resection
Time frame: Up to 1 month
Pathologic examination of the resected specimen for resection margins positivity
Time frame: Up to 1 month
Pathologic examination of the resected specimen (malignant cases)
Time frame: Up to 1 year
After transanal surgery; using the Cleveland Clinic Incontinence Score (Wexner's Score)
Time frame: Up to 1 year
After transanal surgery; using the validated Chinese version of the Fecal Incontinence Quality of Life Scale (FIQL)
Time frame: Up to 1 year
After radical prostatectomy; assessed by recording the number of pads used per day
Time frame: Up to 1 year
After radical prostatectomy; using the abridged version of the International Index of Erectile Dysfunction - erectile function domain score (IIEF-EF)
Time frame: Up to 1 year
After nephrectomy; using renal function blood tests for urea and creatinine
Time frame: Up to 1 year
After TORS; using the MD Anderson Dysphagia Inventory
Time frame: Up to 1 year
After TORS; using the Voice Handicap Index (VHI) 30
Chinese University of Hong Kong
Other
A Novel Robotic System for Single Port and Natural Orifice Transluminal Endoscopic Surgery: A Prospective, Single Center, Multispecialty Study
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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