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Rationale:
Preoperative planning for both partial and radical nephrectomies using conventional CT imaging can be challenging due to complex renal anatomy and vascularization. 3D models in virtual reality (VR) may enhance anatomical understanding and improve preoperative planning. This study aims to prospectively evaluate the clinical impact of the use of 3D models in VR in the preoperative planning of partial and radical nephrectomies.
Objective:
The primary objective is to assess the impact of VR on preoperative planning and thereby on the agreement between the preoperative plan and the performed surgery in renal surgery (both partial and radical nephrectomies). The secondary objectives focus on the urologist's understanding of the anatomy and how the intraoperative and postoperative outcomes are influenced by the use of VR in the preoperative planning.
Study design:
The Virtual Renality study is a single-center randomized clinical trial conducted at the St. Antonius Hospital in Nieuwegein.
Study population:
The study population will consist of adult patients (18+) with a suspected RCC who are indicated for (partial) nephrectomy at St. Antonius Hospital Nieuwegein.
Intervention:
For the intervention group, the urologist will review a 3D virtual model of the renal anatomy in addition to the original CT scan during preoperative planning. For the control group, only the CT scan will be used for preoperative planning, according to the current standard of care.
Main study parameters/endpoints:
The primary study endpoint is the surgical concordance score, which describes the concordance between the actual performed surgery and the preoperatively determined surgical plan.
Nature and extent of the burden and risks associated with participation, benefit, and group relatedness:
Participation in this study will not require any additional physical examinations, blood samples, hospital visits, or questionnaires beyond standard clinical care. The only difference for participants in the intervention group is that a 3D model will be created from the existing CT scan and reviewed in VR during preoperative planning by the urologist.
The Virtual Renality study is a single-center randomized clinical trial conducted at the St. Antonius Hospital in Nieuwegein. For the intervention group, the urologist will review a 3D virtual model of the renal anatomy in addition to the original CT scan during preoperative planning, whereas for the control group, only the CT scan will be used for preoperative planning, according to the current standard of care. The flowchart in Figure 1 provides an overview of the study design. The steps covered in the flowchart and the collection of parameters will be further explained later in this protocol. The study is single-blinded, as the 3D virtual model during preoperative planning is the assessed intervention. Participants will be randomly assigned to either the control group or the intervention group to eliminate selection bias and achieve comparability between the two groups. The urologists who perform (partial) nephrectomies at the St. Antonius Hospital will participate in the study. A total of 72 patients suspected of having a renal tumor and indicated for (partial) nephrectomy will be included. The inclusion period for the study will take approximately 7 months.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Preoperative planning based on CT | No Intervention | For the control group the preoperative planning will be according to the current standard of care using only the CT scan. | |
| Preoperative planning based on CT + VR | Experimental | For the intervention group, the urologist will review a 3D virtual model of the renal anatomy in addition to the CT scan during preoperative planning |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Virtual reality | Device | If the participant is assigned to the intervention group a 3D virtual model will be constructed. For the intervention group the CT + VR will be reviewed during preoperative planning. |
| Measure | Description | Time Frame |
|---|---|---|
| Concordance score between actual performed surgery and surgical plan | To assess whether the surgery is performed according to the preoperative plan, a questionnaire regarding the expected surgical steps will be completed during the preoperative planning. Postoperatively, the data will be collected from the surgical notes. The postoperative data will be compared with the preoperatively filled questionnaire and this will result in a concordance score between the actual performed surgery and the preoperatively determined surgical plan. This score of concordance will be the primary study endpoint | during preoperative planning (approximately 3 days before surgery) and immediately after surgery |
| Measure | Description | Time Frame |
|---|---|---|
| Intra-operative parameters: method of clamping | Method of clamping (main renal artery / multiple arteries / no clamping / selective clamping) | Perioperative |
| Intraoperative parameters: blood loss |
| Measure | Description | Time Frame |
|---|---|---|
| Demographic data - age | Age (Years (at time of surgery) ) | before surgery |
| Demographic data - gender | Gender (Male / Female ) | before surgery |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Emma Trouw, BSc | Contact | 0031616501192 | e.trouw@antoniusziekenhuis.nl |
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| ID | Term |
|---|---|
| D002292 | Carcinoma, Renal Cell |
| D007680 | Kidney Neoplasms |
| ID | Term |
|---|---|
| D000230 | Adenocarcinoma |
| D002277 | Carcinoma |
| D009375 | Neoplasms, Glandular and Epithelial |
| D009370 | Neoplasms by Histologic Type |
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blood loss (value in ml)
| Perioperative |
| Intraoperative parameters: clamping time | clamping time (value in mm:ss) | Perioperative |
| Intraoperative parameters: opening of collecting system | opening of collecting system (yes/no) | Perioperative |
| Intraoperative parameters: duration of surgery | duration of surgery (value in minutes) | Perioperative |
| Post-operative parameters: renal function | Renal function (Creatinine level before surgery, 1 day post-surgery and 4 weeks post-surgery ) | Up to 1 month post-surgery |
| Post-operative parameters: 30-day post-surgery complications | 30-day post-surgery complications ( Clavien Dindo score (Grade I / Grade II / Grade IIIa / Grade IIIb / Grade IVa / Grade IVb / Grade V) ) | 30 days post-surgery |
| Post-operative parameters: hospital stay | hospital stay (days) | 30-days post-surgery |
| Post-operative parameters: readmission (within 30 days) | readmission (within 30 days) (yes/no) | 30-days post-surgery |
| Post-operative parameters: clean resection margin | clean resection margin (yes/no) | 30-days post-surgery |
| Post-operative parameters: | pathological TNM (TxNxMx) | 30-days post-surgery |
| Understanding of anatomy - renal arteries | Understanding of renal arteries (Very poor / Poor / Moderate / Good / Excellent) | during preoperative planning (approximately 3 days before surgery) and immediately after surgery |
| Understanding of anatomy - renal veins | Understanding of renal veins (Very poor / Poor / Moderate / Good / Excellent) | during preoperative planning (approximately 3 days before surgery) and immediately after surgery |
| Understanding of anatomy - collecting system | Understanding of collecting system (Very poor / Poor / Moderate / Good / Excellent) | during preoperative planning (approximately 3 days before surgery) and immediately after surgery |
| Understanding of anatomy - tumor | Understanding of tumor anatomy (Very poor / Poor / Moderate / Good / Excellent) | during preoperative planning (approximately 3 days before surgery) and immediately after surgery |
| Understanding of anatomy - general anatomy | Confidence in understanding of general anatomy (Strongly disagree / Disagree / Neutral / Agree / Strongly agree) | during preoperative planning (approximately 3 days before surgery) |
| Medical data - BMI | BMI (Kg/m2) | before surgery |
| Medical data - ASA-score | ASA-score ( I / II / III / IV / V) | before surgery |
| Medical data - history of smoking | History of smoking (Packyears (or yes/no) ) | before surgery |
| Medical data - comorbidities | Comorbidities (Charlson comorbidity index, 0-37)) | before surgery |
| Medical data - radiological TNM | Radiological TNM classification (TxNxMx ) | before surgery |
| Medical data - RENAL | RENAL score (4-12 a/p/h) | before surgery |
| Medical data - tumor side | Side of tumor(Left/right) | before surgery |
| Medical data - tumor size | Size of tumor (mm) | before surgery |
| Medical data - CT type | Type of CT (Contrast enhanced (which phases)/photon counting) | before surgery |
| Medical data - surgeon | Surgeon (Name / number ) | before surgery |
| D009369 | Neoplasms |
| D014571 | Urologic Neoplasms |
| D014565 | Urogenital Neoplasms |
| D009371 | Neoplasms by Site |
| D052776 | Female Urogenital Diseases |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D007674 | Kidney Diseases |
| D014570 | Urologic Diseases |
| D052801 | Male Urogenital Diseases |