Post Marketing Surveillance for PROSENSE a Cryotherapy Treatment of Renal Cell Carcinoma

  • End date
    Jan 10, 2025
  • participants needed
  • sponsor
    IceCure Medical Ltd.
Updated on 10 September 2020


This experiment is designed for post marketing data collection of a cryosurgical system [PROSENSE of IceCure Medical], for the treatment of renal cell carcinoma (RCC).


A post marketing data collection of a cryosurgical system [PROSENSE] of IceCure Medical], for the treatment of renal cell carcinoma (RCC).

Clinical Study IdentifierNCT02399124
SponsorIceCure Medical Ltd.
Last Modified on10 September 2020

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Inclusion Criteria

Is your age greater than or equal to 18 yrs?
Gender: Male or Female
Do you have any of these conditions: Renal Cell Cancer or Kidney Cancer or Malignant neoplasm of kidney or Malignant Adenoma or Renal Cancer or Adenocarcinoma or Renal Cell Carcinoma?
Patient is above 18 years old
The patient has enhanced solid mass of renal origin located in the kidney or elsewhere proved by imaging
Patient's mass size is up to 5 cm at its largest dimension
Patient is able to visit the clinic as needed during the 60-month follow-up period following the cryoablation procedure
The patient has been informed of the study and agrees to its provisions, and has signed an IRB approved written informed consent, including data privacy authorization

Exclusion Criteria

Patients with permanent coagulation disorders or severe medical instability or active infection
Patients with any terminal illness
Patient participating in other trials using drugs or devices
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Step 2 Get screened

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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Step 3 Enroll in the clinical study

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Step 4 Get your study results

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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