Percutaneous Cryoablation Versus Partial Nephrectomy for T1b Renal Tumor
- Conditions
- Renal Tumor
- Registration Number
- NCT04506671
- Brief Summary
- The aim of our study is to assess the long-term oncological and functional outcomes of cryoablation for T1b renal tumors, as well as such important parameters as the patient's quality of life after treatment, and to compare the results with those after partial nephrectomy. 
- Detailed Description
- Not available 
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 142
•CT-confirmed renal mass > 4 to 7 cm (T1b)
- Multiple renal tumors;
- Recurrence of renal tumor;
- Intolerance to iodine-containing contrast agents;
- Pregnancy;
- Patients with Bosniak 4 cysts
- Presence of other oncological diseases;
- Impossibility of organ-preserving treatment due to the proximity of the tumor to the vessels or the calyx-pelvic system
- Absence of malignant pathology based on prior biopsy.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
- Name - Time - Method - Local recurrence - 5 years - Local recurrance will be evaluated with CT after 6 months, a year, then annually - up to 5 years after the treatment 
- Secondary Outcome Measures
- Name - Time - Method - Metastatic progression - 5 years - Presence of metastases will be evaluated with CT after 6 months, a year, then annually - up to 5 years after the treatment - Length of hospital stay - 1 month - Number of days spent in hospital - Quality of life assessment: The European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ C-30) - 5 years - Quality of life will be assessed using scales EORTC QLQ C-30, ranging from 1 to 100, where higher score indicating a better Quality of Life - Pain score - 5 years - Pain score will be assessed using visual analogue scale - Renal function - 5 years - Renal function will be evaluated with eGFR - Rate of adverse events - 3 months - Rate of intra- and postoperative adverse events will be assessed according to Clavien-Dindo grade system - Blood loss - 12 months - Pre- and postoperative Hb level 
Trial Locations
- Locations (1)
- Institute for Urology and Reproductive Health, Sechenov University. 🇷🇺- Moscow, Russian Federation Institute for Urology and Reproductive Health, Sechenov University.🇷🇺Moscow, Russian FederationDmitry Enikeev, M.D., Ph.DContact+7 9670897154enikeev-dv@1msmu.ruMark Taratkin, MDContact+7 9670897154marktaratkin@gmail.com
