Renal Tumor Clinical Trial
Official title:
A Prospective, Non-randomized, in Parallel Groups Study Evaluating the Efficacy and Safety of Percutaneous Cryoablation and Partial Nephrectomy in Localized T1b Renal Tumor
NCT number | NCT04506671 |
Other study ID # | CA_vs_PN |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | May 22, 2020 |
Est. completion date | June 22, 2025 |
Verified date | July 2021 |
Source | I.M. Sechenov First Moscow State Medical University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Recruiting |
Enrollment | 142 |
Est. completion date | June 22, 2025 |
Est. primary completion date | May 22, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: •CT-confirmed renal mass > 4 to 7 cm (T1b) Exclusion Criteria: - 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. |
Country | Name | City | State |
---|---|---|---|
Russian Federation | Institute for Urology and Reproductive Health, Sechenov University. | Moscow |
Lead Sponsor | Collaborator |
---|---|
I.M. Sechenov First Moscow State Medical University |
Russian Federation,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Local recurrence | Local recurrance will be evaluated with CT after 6 months, a year, then annually - up to 5 years after the treatment | 5 years | |
Secondary | Metastatic progression | Presence of metastases will be evaluated with CT after 6 months, a year, then annually - up to 5 years after the treatment | 5 years | |
Secondary | Quality of life assessment: The European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ C-30) | 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 | 5 years | |
Secondary | Renal function | Renal function will be evaluated with eGFR | 5 years | |
Secondary | Rate of adverse events | Rate of intra- and postoperative adverse events will be assessed according to Clavien-Dindo grade system | 3 months | |
Secondary | Blood loss | Pre- and postoperative Hb level | 12 months | |
Secondary | Length of hospital stay | Number of days spent in hospital | 1 month | |
Secondary | Pain score | Pain score will be assessed using visual analogue scale | 5 years |
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