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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04814758
Other study ID # NCPHOI-2019-08
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date December 21, 2020
Est. completion date December 21, 2023

Study information

Verified date February 2021
Source Federal Research Institute of Pediatric Hematology, Oncology and Immunology
Contact Evelina f Nazarova
Phone +79161133945
Email evelina.nazarova@fccho-moscow.ru
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Initially, or after preoperative chemotherapy, patients with a kidney tumor are examined on 3T MR scanner or 1.5T MR scanner. A standard MRI study of the abdomen with contrast enhancement is performed. DWI (diffusion weighted) images are included in the standard investigation package and consist of diffusion maps. Then, using Philips workstation (ISP 9.0, Philips, Netherlands), DWI mapping and ADC values collection (mm2/s) are performed. The placement of region of interest (ROI) is selected in the kidney mass in a solid and cystic area with a size up to 100 mm2. After the preoperative abdomen MRI, a surgical treatment is performed. Histological material is directed to the pathologist, who carried out the histological staging by the malignancy degree (low, intermediate, high). The data is entered into the database and the relationship between ADC values and histological degrees of malignancy of nephroblastoma is investigated


Description:

Initially, or after preoperative chemotherapy, patients with a kidney tumor are examined on 3T MR scanner or 1.5T MR scanner, using 8-channel body coil. A standard MRI study of the abdomen with contrast enhancement is performed. DWI (diffusion weighted) images are included in the standard investigation package and consist of diffusion maps (DWI 3b) with 3 b-factors (50; 600; 800 or others, optional). Then, using Philips workstation (ISP 9.0, Philips, Netherlands), DWI mapping and ADC values collection (mm2/s) are performed. The placement of region of interest (ROI) is selected in the kidney mass in a solid and cystic area with a size up to 100 mm2. The values are entered in the table due to the stage of the chemotherapy. After the preoperative abdomen MRI, a surgical treatment is performed. Histological material is directed to the pathologist, who carried out the histological staging by the malignancy degree (low, intermediate, high). The data is entered into the database and the relationship between ADC values and histological degrees of malignancy of nephroblastoma is investigated.


Recruitment information / eligibility

Status Recruiting
Enrollment 230
Est. completion date December 21, 2023
Est. primary completion date December 21, 2023
Accepts healthy volunteers No
Gender All
Age group N/A to 18 Years
Eligibility Inclusion Criteria: 1. Age under 18 y.o.; 2. Renal mass with confirmed histology. Exclusion Criteria: 1. Absolute contraindications to magnetic resonance imaging (pacemaker, ferromagnetic implants, etc.); 2. Refusal to sign the informed consent.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
MRI DWI sequence (ADC values)
Initially and after pre-operative chemotherapy To evaluate the differences in ADC values according to the malignancy degree of nephroblastoma in children

Locations

Country Name City State
Russian Federation Dmitry Rogachev National Medical Research Centre of Pediatric Hematology, Oncology and Immunology Moscow

Sponsors (1)

Lead Sponsor Collaborator
Federal Research Institute of Pediatric Hematology, Oncology and Immunology

Country where clinical trial is conducted

Russian Federation, 

Outcome

Type Measure Description Time frame Safety issue
Primary To evaluate the differences in ADC values according to the malignancy degree of nephroblastoma in children Point 1. 15 ± 3 days Before the start of therapy - the starting point.
Primary To evaluate the differences in ADC values according to the malignancy degree of nephroblastoma in children Point 2. after pre-operative chemotherapy up to 1 week
Secondary To evaluate the reproducibility and compatibility of the ADC values measurement; Point 1. 15 ± 3 days Before the start of therapy - the starting point.
Secondary To evaluate the reproducibility and compatibility of the ADC values measurement; Point 2. after pre-operative chemotherapy up to 1 week
Secondary To assess the sensitivity and specificity of the MRI DWI sequence (ADC values) in the diagnosis of the malignancy degrees of nephroblastomas in children; Point 1. 15 ± 3 days Before the start of therapy - the starting point.
Secondary To assess the sensitivity and specificity of the MRI DWI sequence (ADC values) in the diagnosis of the malignancy degrees of nephroblastomas in children; Point 2. after pre-operative chemotherapy up to 1 week
Secondary To estimate the differences in ADC values within the intermediate degree of nephroblastoma malignancy in children Point 1. 15 ± 3 days Before the start of therapy - the starting point.
Secondary To estimate the differences in ADC values within the intermediate degree of nephroblastoma malignancy in children Point 2. after pre-operative chemotherapy up to 1 week
Secondary To assess the ADC values change in depending according to the provided chemotherapy. Point 1. 15 ± 3 days Before the start of therapy - the starting point.
Secondary To assess the ADC values change in depending according to the provided chemotherapy. Point 2. after pre-operative chemotherapy up to 1 week