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A Prospective, Single-Center Investigation of the da Vinci SP® Surgical System in Anterior Mediastinal Disease

A Prospective, Single-Center Investigation of the da Vinci SP® Surgical System in Anterior Mediastinal Disease

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05455840
Enrollment
15
Registered
2022-07-13
Start date
2022-08-03
Completion date
2024-04-11
Last updated
2023-10-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myasthenia Gravis, Robotic Surgical Procedure, Thymoma

Keywords

single incision robotic minimal invasive surgery, robotic mediastinal tumor resection, da Vinci SP® surgical system

Brief summary

Endpoints (Outcome measures): 1. Primary endpoint: Incidence of conversion rate during surgery \- The primary performance endpoint will be assessed as the ability to successfully complete the planned mediastinal procedure with da Vinci SP System, with no conversion to open surgery, video-assisted thoracoscopic surgery (VATS), multi-port robotic surgery or approach requiring undocking of the da Vinci SP Surgical System in order to complete the planned procedure using the alternate approach. Use of additional assistant port(s) is not considered a conversion 2. Secondary endpoints: Incidence of treatment related adverse events - The safety endpoint will be assessed as the incidence of all intra-operative and post-operative adverse events that occur through the 30-day follow up period

Detailed description

During the past several years, minimally invasive thoracic surgery has evolved from thoracoscopic approaches using 3 -4 ports to a single incision video-assisted thoracoscopic surgery (VATS) techniques. Recently, the experience acquired with the uniportal VATS technique through the intercostal space has allowed the development of a uniportal VATS subxiphoid or subcostal approach for anterior mediastinal tumor resections. The advantage of using a subxiphoid or subcostal entry is to reduce pain by avoiding possible trauma of intercostal nerves caused by thoracic incisions. However, the longer distance from the subxiphoid or subcostal incision to the anterior mediastinal area makes this approach more difficult to perform extended thymothymectomy. During this same period of evolution into uniportal VATS surgery, robotic thoracic surgery has gained popularity as an alternative to traditional VATS. The advantages of robotics are the ability to perform surgery more precisely with articulated or wristed instruments, motion scaling, and tremor filtration, as well as improved visualization thanks to 3D high-definition video. However, currently 4 -5 incisions are still necessary to perform anatomic robotic resections.Recently, there has been a convergence of these two trends-uniportal surgery and robotic-assisted surgery-and has resulted in a single port robotic system, the da Vinci SP by Intuitive Surgical Cooperation. For this new platform, investigators plan to practice in extended thymothymectomy

Interventions

DEVICEDa Vinci SP surgical platform

using Da Vinci SP platform in thymothymectomy or extended thymectomy

Sponsors

Chang Gung Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

thymothmectomy or extended thymectomy through Da Vinci SP platform

Eligibility

Sex/Gender
ALL
Age
20 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Age \>20 and \<75 years-old 2. Willing and able to provide informed consent 3. ASA≤ 3 4. The subject fulfills one or both of the following criteria: * Diagnosis of myasthenia gravis * Masaoka stage I or II thymoma; thymic mass ≤ 5 cm diameter 5. Class I-IV Myasthenia gravis according to the Myasthenia Gravis Foundation of America Scientific Session (MGFA)

Exclusion criteria

. Myasthenia gravis or thymoma patients with 1. Congestive heart failure (NHYA \> II) 2. Arrhythmia required medication control 3. Subjects with a known bleeding or clotting disorder 4. Subjects actively receiving therapeutic dose anticoagulation or anti-platelet medications at the time of operation 5. Subjects under immunomodulatory within 30 days prior to the planned surgery 6. Previous ipsilateral thoracic surgery or sternotomy 7. Uncontrolled illness 6 months prior to planned surgical procedure including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements 8. Previous neoadjuvant medical and/or radiation therapy 9. Subject has a contraindication for general anesthesia or surgery 10. Uncontrolled myasthenia gravis symptoms at the time of scheduled surgery 11. Confirmed thymic carcinoma 12. Patients who are not suitable for performing endoscopic surgery. 13. Myasthenia gravis patients with positive serum MuSK antibody. -

Design outcomes

Primary

MeasureTime frameDescription
Incidence of conversion rateDuring SurgeryThe primary performance endpoint will be assessed as the ability to successfully complete the planned procedure with da Vinci SP System, with no conversion to thoracoscopic, multi-port robotic, or open surgery.

Secondary

MeasureTime frameDescription
Incidence of Treatment-Emergent Adverse EventsOne yearThe safety endpoint will be assessed as the incidence of all intra-operative and post-operative adverse events that occur through the 30-day follow up period. Rceord the Incidence of Treatment-Emergent Adverse Events in our recording form

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 3, 2026