Kidney Cancer Clinical Trial
— RESTARTOfficial title:
Resection or Ablative Treatment of Small Renal Tumors, a Multicenter Randomized Clinical Trial
NCT number | NCT06278506 |
Other study ID # | 4612 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | January 31, 2024 |
Est. completion date | December 2037 |
Ablative treatments are believed to have a lower rate of complications, shorter hospital stays, and fewer interventions with benign PAD compared to partial nephrectomies in small kidney cancer lesions. The purpose of the study is to compare complications, the frequency of residual tumors, impact on kidney function, differences in quality of life, and health economic factors in a randomised study. We will also compare the oncological outcomes, including survival and recurrence of kidney cancer.
Status | Recruiting |
Enrollment | 300 |
Est. completion date | December 2037 |
Est. primary completion date | December 2027 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 99 Years |
Eligibility | Inclusion Criteria: - Age 18 - 99 years - Patient suitable based on clinical status for both ablative treatment and surgery - Primary kidney tumor - Tumor size = 3 cm - Clinical stage of the tumor T1a (no macroscopic vascular or extrarenal invasion) - Tumor location suitable for both ablative treatment and resection - Absence of radiological signs of metastasis - Biopsy with malignant pathological analysis (PAD) - ISUP grade I-III" Exclusion Criteria: - Radiological signs of metastasis - Synchronous kidney tumors - ISUP grade IV or sarcomatoid growth in the biopsy - Other metastasized cancer in the last 5 years - Patient unable to make an informed decision to participate in the study |
Country | Name | City | State |
---|---|---|---|
Sweden | Karolinska University Hospital | Stockholm |
Lead Sponsor | Collaborator |
---|---|
Karolinska University Hospital |
Sweden,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of participants with surgical complications according to Clavien-Dindo grade 2-5 | recorded through chart review at 30 and 90 days after treatment. Complications are summed up in case of retreatment before the 12-month follow-up. | First year after inclusion | |
Primary | Radiological signs of a residual tumor at the 6-month follow-up | Radiological sign of residual tumor at 6-month radiology | 6-month after inclusion | |
Primary | Number of postoperative hospitalization days (LOS) | Number of postoperative hospitalization days (LOS), i.e., the time the patient has been hospitalized after the procedure until discharge. Hospitalization time is accumulated in case of retreatment within 12 months. | Sum of total after all interventions first year after the first intervention | |
Secondary | Cancer-specific survival (CSS) | Cancer-specific survival (CSS) is the period from cancer diagnosis to death caused by this cancer diagnosis. CSS will be calculated using Kaplan-Meier estimates and cumulative incidence of cancer-specific death. | 2, 5 and 10 years after inclusion | |
Secondary | Overall survival (OS) | State of survival | 2, 5 and 10 years after inclusion | |
Secondary | Change in eGFR one year after treatment | The study aims to assess kidney function impairment one year after treatment. Blood tests for estimated glomerular filtration rate (eGFR) will be compared with preoperative values to monitor changes. Impaired function is defined as eGFR reduction by =20% one year after the procedure compared to measurements before treatment for kidney tumors (10). | One year after inclusion |
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