Clinical trial · Interventional
Feasibility of RUS Lung in MITS
Feasibility and Efficacy of Surgical Navigation 'RUS Lung' in Patients Undergoing Minimally Invasive Thoracic Surgery (MITS) Segmentectomy for Lung Cancer: a Multicenter Prospective Observational Study With a Propensity-score Matching Analysis
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This sponsor-initiated prospective observational study aims to demonstrate the feasibility and efficacy of RUS Lung Surgical Navigation System in patients undergoing minimally invasive thoracic surgery(MITS). The trial will enroll 36 patients who undergo video-assisted or robot-assisted thoracoscopic surgery using RUS Lung. The study will be conducted across two medical centers." * Investigational Medical Device: RUS Lung (Endoscopic Imaging Treatment Planning Software) * Clinical Trial duration: 12 months from IRB approval * Target number of subjects: Total of 36 participants
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Lung Cancer | Malignant Lung Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| RUS Lung | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- RUS Group
- description
- Patients undergo video-assisted or robot-assisted thoracoscopic surgery using RUS Lung software.
- interventionNames
- Device: RUS Lung
Primary outcomes (1)
- measure
- The concordance rate of tumor location across CT, RUS Lung, and surgery
- timeFrame
- The operative day (operative day ± 5 days)
- description
- Overall feasibility of the RUS Lung system will be evaluated by 3 factors as below. 1. CT turn-around time: the duration between uploading of preoperative CT and downloading the 3D model file 2. The stability of the RUS Lung system 3. The concordance rate of tumor location across CT, RUS Lung, and surgery
Secondary outcomes (1)
- measure
- The degree of consistency between surgical planning using the RUS lung system and actual surgical findings.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 19 Years
Show eligibility criteria text
Inclusion Criteria: * Individuals who were diagnosed with lung caner (tumor size≤3cm) * Individuals aged 19 or older * Individuals who who are able to undergo CT imaging according to the established protocol * Individuals who have voluntarily given written consent to participate in this clinical trial Exclusion Criteria: * Vulnerable subjects * Individuals who who are not able to undergo CT imaging according to the established protocol * Individuals who are expected to have severe adhesions * Individuals who are unable to follow the study procedures and are deemed inappropriate for participation
References
Publications (0)
Data not yet available