NCT07004426

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jun 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 27, 2025

Completed
5 days until next milestone

Study Start

First participant enrolled

June 1, 2025

Completed
3 days until next milestone

First Posted

Study publicly available on registry

June 4, 2025

Completed
27 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2025

Completed
14 days until next milestone

Study Completion

Last participant's last visit for all outcomes

July 15, 2025

Completed
Last Updated

March 19, 2026

Status Verified

July 1, 2025

Enrollment Period

1 month

First QC Date

May 27, 2025

Last Update Submit

March 17, 2026

Conditions

Keywords

Renal cell carcinomaDetectionImaging modalitiesNon-neoplastic renal lesions

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

Procedure: Surgical treatment of renal lesions

Interventions

Surgical treatment of renal lesions

A single patient group undergoing intervention for renal lesions

Eligibility Criteria

Age18 Years - 90 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Location

MeSH Terms

Conditions

Carcinoma, Renal CellKidney Neoplasms

Condition Hierarchy (Ancestors)

AdenocarcinomaCarcinomaNeoplasms, Glandular and EpithelialNeoplasms by Histologic TypeNeoplasmsUrologic NeoplasmsUrogenital NeoplasmsNeoplasms by SiteFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesKidney DiseasesUrologic DiseasesMale Urogenital Diseases

Study Officials

  • Jindřich Šonský, MD

    Vascular surgery, University hospital Královské Vinohrady, Prague

    PRINCIPAL INVESTIGATOR
  • Alexandra Gregušová, MD

    Vascular surgery, University hospital Královské Vinohrady, Prague

    STUDY CHAIR
  • Jakub Hanych, MD

    Vascular surgery, University hospital Královské Vinohrady, Prague

    STUDY CHAIR
  • Robert Grill, assoc. prof., MD, PhD

    Vascular surgery, University hospital Královské Vinohrady, Prague

    STUDY DIRECTOR
  • 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 CHAIR

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

The data that support the findings of this study will be available from the principal investigators upon reasonable request.

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.

Locations