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Cryaoablation Assisted Partial Nephrectomy a Non Ischemic Approach

Cryotherapy and Robotic Assisted Non Ischemic Nephron Sparring Surgery

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05218811
Acronym
RCAPN
Enrollment
150
Registered
2022-02-01
Start date
2020-05-15
Completion date
2041-05-15
Last updated
2023-01-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Kidney Neoplasms

Brief summary

Patients with renal masses eligible to partial nephrectomy often require arterial ischemia to control or prevent blood loss during this surgical procedure. This study aims to determine the safety and efficacy of renal cryoablation at the tumor bed, as a substitute measure or technique vs total or selective arterial renal ischemia.

Detailed description

Nephron sparring surgery has emerged as the procedure of choice for most patients with renal tumors that are \>2 cm and harbor a greater than 50% exophitic component. In order to decrease blood loss surgeons may: 1- interrupt blood flow to the kidney, completely or selectively; 2-Use diuretics such as mannitol to dehydrate the kidney; 3-Ice externally the kidney - in open procedures - to decrease metabolism during ischemia. The emergence of robotic surgery triggered a shift in the the surgical approach to partial nephrectomy and is commonly employed. A fundamental drawback of this technique is represented on the lack of cold ischemia. However, warm ischemia is commonly employed and requires dissection of the renal pedicle, which by itself puts the kidney at risk of loss.

Interventions

DEVICECryoablation Assisted Partial Nephrectomy

Cryoablation Assisted Partial Nephrectomy is monitored under Ultrasound guidance, A Cryoablation machine (FDA Approved Device) along with its Cryoprobes are used in the study The Cryoprobes are placed in close to the endophytic tumor margins. The tumor boundary area will undergo one freezing cycles. Tumor is excised after 5 minutes of freezing cycle. Thawing process is passive, renal defect repair is conducted during thawing process.

Sponsors

Urological Research Network, LLC
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Patients are scheduled for a surgical procedure: robotic partial nephrectomy, and the investigators will use a cryoablation probe(s) for selective ischemia rather than full blood flow interruption with a vascular clamp

Eligibility

Sex/Gender
ALL
Age
55 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Patients with ages between 45-90-year-old. * Renal tumor ≤ 7 cm in the greatest extension, \>50% exophitic.

Exclusion criteria

* Prior renal surgery * M1 Disease

Design outcomes

Primary

MeasureTime frameDescription
Recurrence - Oncological Control10 YearsRecurrence at Site of Excision or within 1 cm of margin or Development of Metastasis

Secondary

MeasureTime frameDescription
Local Re-Intervention10 YearsEither subsequent ablation or surgical exploration or surgical kidney removal
Development or Progression of Chronic Kidney Disease (CKD)10 YearsDe-Novo emergence of CDK or changes in CKD overtime based on variation from baseline. The international classification for CKD defined by serum estimated Glomerular Filtration Rates (GFR) will be used as measurement instrument using the following definitions: GFR categories in CKD G1 ≥90 Normal or high G2 60-89 Mildly decreased\* G3a 45-59 Mildly to moderately decreased G3b 30-44 Moderately to severely decreased
Incidence of Metastatic disease10 Yearspatients will be evaluated using imaging studies at fixed intervals as follows: at 6 months Renal Ultrasound at 1 year CT Urogram at 18 Months, 24 months and yearly thereafter with Renal Ultrasound CT Urograms will be performed as needed for cause
Survival10 yearsIf a patient expiries during the study interval we would procure the death certificate and do our best to determine cause of death

Countries

United States

Contacts

Primary ContactEusebio J Luna, MD
drluna@research.surgery3058227227
Backup ContactCielo Guerra
cielo@besturology.net3058227227

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026