Symptomatic and Incidental RCC Detection
KIDCaD
Assessment of Symptomatic and Incidental Detection of Renal Cell Carcinoma Using Standard Imaging Modalities
1 other identifier
observational
1,000
1 country
1
Brief Summary
Evaluation of the frequency of symptomatic and incidental detection of renal carcinoma at different stages depending on the imaging modality used
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jun 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 27, 2025
CompletedStudy Start
First participant enrolled
June 1, 2025
CompletedFirst Posted
Study publicly available on registry
June 4, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
July 15, 2025
CompletedMarch 19, 2026
July 1, 2025
1 month
May 27, 2025
March 17, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Detection-specific renal cell carcinoma (RCC) proportions
Detection-specific renal cell carcinoma (RCC) proportions, defined as the proportion of each detection type relative to all RCC cases. Results will be stratified by stage, histological type, and imaging modality.
From 2011 to 2020
Secondary Outcomes (1)
Proportion of RCC among neoplastic and non-neoplastic renal lesions
From 2011 to 2020
Study Arms (1)
A single patient group undergoing intervention for renal lesions
Interventions
Surgical treatment of renal lesions
Eligibility Criteria
Patients treated for renal lesions at the Urology Department of University Hospital Královské Vinohrady
You may qualify if:
- patients over 18 years of age undergoing surgical treatment for renal lesions
You may not qualify if:
- patients undergoing surgery for non-renal and urotelial carcinoma, including unknown
- patients with recurrent renal lesions
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University Hospital Královské Vinohrady
Prague, 100 34, Czechia
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jindřich Šonský, MD
Vascular surgery, University hospital Královské Vinohrady, Prague
- STUDY CHAIR
Alexandra Gregušová, MD
Vascular surgery, University hospital Královské Vinohrady, Prague
- STUDY CHAIR
Jakub Hanych, MD
Vascular surgery, University hospital Královské Vinohrady, Prague
- STUDY DIRECTOR
Robert Grill, assoc. prof., MD, PhD
Vascular surgery, University hospital Královské Vinohrady, Prague
- STUDY CHAIR
Kateřina Licková, MD, PhD
Vascular surgery, University hospital Královské Vinohrady, Prague
- STUDY CHAIR
Jana Malinová, MD, PhD
Vascular surgery, University hospital Královské Vinohrady, Prague
- STUDY CHAIR
Tomáš Blažek, MD, PhD
Ostrava University Hospital
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 1 Day
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 27, 2025
First Posted
June 4, 2025
Study Start
June 1, 2025
Primary Completion
July 1, 2025
Study Completion
July 15, 2025
Last Updated
March 19, 2026
Record last verified: 2025-07
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- CSR
- Time Frame
- planned from August 2025 for a period of 5 years
- Access Criteria
- The data that support the findings of this study will be available from the principal investigators upon reasonable request.
The data that support the findings of this study will be available from the principal investigators upon reasonable request.