Linkou Chang Gung Memorial Hospital
Taoyuan, Taiwan
NCT Number: NCT06766760
This prospective, interventional, non-randomized, single arm, clinical trial will investigate feasibility and safety of trans-oral robotic surgery using da Vinci SP Surgical System in Taiwan for the surgical treatment of OSA. All the investigators are well trained and have received proof of training after completing the training program for da Vinci SP system provided by Intuitive.
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Not applicable
Taoyuan, Taiwan
This study will be conducted in Chang Gung Memorial Hospital at Linkou.
Informed consent will be provided to patient who has an indication of surgical treatment for OSA. Study participants will sign an informed consent before any study procedure begins. Eligibilities will be assessed during screening period (2 weeks) with blood test and other routine assessments. Eligible patient will undergo surgical intervention using da Vinci SP Surgical System. Post-operation follow-up will be performed at 1 week, 1 month, 3 months, and 6 months.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The da Vinci SP Surgical System is intended to assist in the accurate control of the da Vinci SP endoscope and instruments during minimally invasive endoscopic abdominopelvic, thoracoscopic, transoral otolaryngology, and breast surgical procedures. The system is indicated for adult use. It is intended to be used by trained physicians in an operating room environment.
Time frame: 3 months (+60 days) post-surgery
Success of tongue base resection without conversion to alternative surgery
Time frame: 3 months (+60 days) post-surgery
Type I PSG measurements demonstrating Apena Hypopnea Index (AHI) reduction. An AHI of < 20 events/hour and a reduction in AHI of 50% or greater from baseline levels will be defined as success, when evaluated at 3 months (+60 days) post-surgery. Although it does not meet these criteria, it can be interpreted as an "improved" result when AHI is improved after surgery.
Time frame: Intraoperative
Multi-level surgery (procedure used)
Time frame: 3 months (+60 days) post-surgery
Snoring VAS
Time frame: Intraoperative
Operative time (first skin incision to closure of wound)
Time frame: 3 months (+60 days) post-surgery
Console time
Time frame: 3 months (+60 days) post-surgery
Transfusion and estimated blood loss
Time frame: 3 months (+60 days) post-surgery
Length of hospital stay
Time frame: 30 days
Rate, intraoperative and/or postoperative, Clavien system
Time frame: 30 days
Readmission rate
Time frame: 30 days
Reoperation rate
Time frame: 30 days
Perioperative mortality
Time frame: 3 months (+60 days) post-surgery
measured using the volume displacement method
Time frame: 3 months (+60 days) post-surgery
Pain score (VAS)
Time frame: 3 months (+60 days) post-surgery
Epworth Sleepiness Scale (ESS) and Stanford Sleepiness Scale (SSS) at 3 months (+60 days) post-surgery compared to baseline
Time frame: at 1, 3, 6 months post-surgery
Pittsburgh Sleep Quality Index (PSQI) at 1, 3, 6 months post-surgery compared to baseline.
Time frame: within 3 months (+60 days) post-surgery
Assessment of all reported adverse events (AE) within 3 months, (+60 days) post-surgery. Summarizing the incidence and frequency of all reported adverse events and categorizing them using CTCAE.
Time frame: 3 months (+60 days) post-surgery
Imaging analysis for resected tissue volume
Time frame: 3 months (+60 days) post-surgery
Percentages of sleep stages (N1, N2, N3, R), at 3 months (+60 days) post-surgery compared to baseline.
Time frame: 3 months (+60 days) post-surgery
Lowest oxygen saturation (LSAT), at 3 months (+60 days) post-surgery compared to baseline.
Time frame: 3 months (+60 days) post-surgery
Percent sleep time below 90% oxygen saturation (ST90) at 3 months (+60 days) post-surgery compared to baseline.
Contact information is provided by the study sponsor or research team.
Chang Gung Memorial Hospital
Other
A Pilot Study of Single-port Robot-assisted Surgery Using da Vinci SP Surgical System for the Surgical Treatment for Patients With Obstructive Sleep Apnea
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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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