Evaluation of the Efficacy, Safety, and Stability of the Surgical Navigation System 'RUS NE' in Robot-Assisted Partial Nephrectomy: A Retrospective and Prospective Comparative Study
试验速览
- 阶段
- 不适用
- 状态
- Enrolling By Invitation
- 发起方
- 入组人数
- 80
- 试验地点
- 1
- 主要终点
- Resection volume
研究概览
简要总结
This study is a retrospective and prospective comparative study evaluating the efficacy, safety, and stability of the surgical navigation system 'RUS NE' in robot-assisted partial nephrectomy. The study aims to compare intraoperative and postoperative clinical indicators between the experimental group and the control group to verify the clinical effectiveness and stability of RUS NE. This research is conducted as part of the 2025 Corporate Verification Support Project of the Global Innovative Medical Technology Verification Support Center at Asan Medical Center (ARIS Project Number: A20250116) and is supported by the Korea Health Industry Development Institute's healthcare technology research and development program.
详细描述
1. Study Objectives
- Efficacy Evaluation: Comparison of resection volume, operative time, and blood loss between the experimental group (RUS NE-assisted) and the control group (standard procedure).
o Analysis of whether RUS NE facilitates accurate tumor localization to minimize resection margins. 2. Stability Evaluation: Validation of CT turn-around time, accuracy of 3D image reconstruction, and system functionality.
- Assessment of the device's reliability and stability in a real surgical environment. 3. Study Methods
- Study Design: Retrospective and prospective, single-center, comparative study.
- Study Population: Patients scheduled for robot-assisted partial nephrectomy.
- Study Period: From IRB approval to December 31, 2025.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 20 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •[Experimental Group]
- •Patients diagnosed with renal cancer scheduled for robot-assisted partial nephrectomy using the RUS system, aged between 20 and 80 years.
- •Patients who voluntarily consent to participate in this clinical trial and sign the written informed consent form.
- •Patients with a renal tumor measuring ≤10 cm in maximum diameter on preoperative CT imaging.
- •Patients with a RENAL Nephrometry Score between 4 and
- •[Control Group]
- •Patients diagnosed with renal cancer who underwent robot-assisted partial nephrectomy using the standard surgical method at the institution between January 1, 2020, and January 23,
- •Patients aged between 19 and 79 years.
- •Patients with a renal tumor measuring ≤10 cm in maximum diameter on preoperative CT imaging.
- •Patients with a RENAL Nephrometry Score between 4 and 12.
排除标准
- •[Experimental Group]
- •Patients who do not consent to participate in the clinical trial.
- •Patients whose CT examination does not follow the required protocol for image analysis.
- •Patients with a history of abdominal surgery likely to cause severe adhesions.
- •Patients with a solitary kidney or horseshoe kidney as identified on preoperative CT.
- •Patients scheduled for bilateral nephrectomy.
- •Patients requiring simultaneous resection of other organs in addition to nephrectomy.
- •Patients with a history of abdominal surgery where severe adhesions are expected based on the investigator's judgment.
- •Patients with severe renal dysfunction at the time of screening (serum creatinine level ≥1.5 times the upper limit of normal for the study site) or CKD stage 3 (eGFR <60).
- •Patients classified as ASA (American Society of Anesthesiologists Physical Status Classification) IV-VI.
- •Patients with a history of psychiatric disorders, alcohol abuse, or other conditions that, in the investigator's judgment, make clinical trial participation inappropriate.
- •Patients who have participated in or are scheduled to participate in another clinical trial (medical device or pharmaceutical) within four weeks prior to screening.
- •Patients deemed unsuitable for clinical trial participation at the investigator's discretion.
- •Patients whose CT images are not suitable for generating 3D images for use with the investigational medical device.
- •[Control Group]
- •Patients whose CT data are unavailable.
- •Patients with a history of abdominal surgery with expected or confirmed severe adhesions.
- •Patients with a solitary kidney or horseshoe kidney.
- •Patients who have undergone bilateral nephrectomy.
- •Patients who have undergone simultaneous resection of other organs in addition to nephrectomy.
- •Patients with renal dysfunction (serum creatinine level ≥1.5 times the upper limit of normal for the study site) or CKD stage 3 (eGFR <60).
结局指标
主要结局
Resection volume
时间窗: At the time of surgery
Resection volume were measured by ellipsoid formula. The maximum longitudinal length of the resected kidney specimen is measured along the X-axis, with perpendicular measurements taken along the Y and Z axes. The volume is estimated using the formula: (π/6) × X × Y × Z.
次要结局
- Operative time(At the time of surgery)