Cleveland Clinic Taussig Cancer Institute, Case Comprehensive Cancer Center
Cleveland, Ohio, 44195, United States
Location contact
Mohamed Eltemamy, MD
CONTACT
Mohamed Eltemamy, MD
PRINCIPAL_INVESTIGATOR
NCT Number: NCT05725421
This study is designed to investigate a novel approach to offer more ESRD participants the benefits associated with renal transplantation by increasing the supply of available allografts
Trial opening soon.
Get Notified60 year and older
All sexes
Interventional
Not applicable
Cleveland, Ohio, 44195, United States
Mohamed Eltemamy, MD
CONTACT
Mohamed Eltemamy, MD
PRINCIPAL_INVESTIGATOR
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
For Donors:
o Normal baseline renal function, with eGFR > 80 ml/min/1.73 m2
For Recipients:
Exclusion criteria
For Donors:
o < 50 years of age
o Tumor has infiltrative features
o Malignant non-RCC pathology
o Rhabdoid or sarcomatoid differentiation
o Grade 4
o Positive or concerning margins during tumor excision
For Recipients:
Donor participants will undergo laparoscopic radical nephrectomy (RN) . Donor kidney then will undergo cold perfusion and ex-vivo partial nephrectomy (PN) with cold ischemia. During PN, careful inspection of tumor will be performed to ensure it is well-encapsulated. If any infiltrative features (versus well encapsulated tumor) are noted intraoperatively then transplant will not be performed. Multiple surgical margins will be sent (either frozen section or standard with priority). If final margins are positive or concerning, then transplant will not be performed. Biopsies of the tumor will be performed and sent to pathology (either frozen section or standard with priority).
The donor kidney will remain on ice while pathologic analysis is performed, and transplant recipient surgery is initiated (if pathologic analysis satisfactory). Cold ischemia with delay for pathology will have minimal functional impact in this setting based on extensive prior experience with renal transplantation where kidneys are routinely kept hypothermic for several hours prior to transplantation.
Radical nephrectomy consists of the removal of the kidney together with the perirenal fat and regional lymph nodes. The transperitoneal approach allows early control of the renal vessels.
Time frame: Within 30 days of surgery
Safety and feasibility as determined by peri-operative adverse events of the following Grade 3-5 CTCAE v5.0 outcomes within 30 days of surgery:
i. Anemia ii. Acute kidney injury
Time frame: Within 30 days of surgery
Safety and feasibility as determined by peri-operative adverse events of the following Grade 3-5 CTCAE v5.0 outcomes within 30 days of surgery:
i. Anemia ii. Renal hemorrhage iii. Kidney anastomotic leak iv. Urinary fistula
Time frame: Within 180 days of surgery
a. Intermediate term surgical outcomes as determined by adverse events of the following Grade 3-5 CTCAE v5.0 outcomes within 180 days of surgery: i. Anemia ii. Acute kidney injury iii. Wound infection iv. Infection and infestations - Urinary tract infection, abscess
Time frame: 1 year after surgery
Renal function as determined by:
i. Post-operative baseline GFR >45 ml/min/1.73m2 at time of follow up ii. GFR >45 ml/min/1.73m2 at one year after radical nephrectomy
Time frame: Up to 1 year after surgery
c. Oncologic outcomes as determined by local or distant recurrence of malignancy within one year of follow up
Time frame: Within 180 days of surgery
Intermediate term surgical outcomes as determined by adverse events of the following Grade 3-5 CTCAE v5.0 outcomes within 180 days of surgery:
i. Anemia ii. Renal hemorrhage iii. Kidney anastomotic leak iv. Urinary fistula v. Wound infection vi. Infection and infestations - Other, Urinary tract infection, abscess, bacteremia
Time frame: 1 year after surgery
Renal function as determined by:
i. Delayed-graft function ii. Nadir post-transplant GFR iii. GFR measured at one year follow up
Time frame: Up to 1 year after surgery
c. Oncologic outcomes as determined by local or distant recurrence of malignancy within one year of follow up, diagnosed by one year follow up CT imaging or other method used to determine presence of recurrent malignancy
Time frame: 1 year after surgery
Participant attitudes and decision making surrounding altruistic donation as a component of surgery for a renal mass will be determined by a survey provided to participants at a preoperative visit prior to surgery and at the 12 month follow-up visit.
Time frame: 1 year after surgery
Participant attitudes and decision-making surrounding receipt of a kidney that previously had a small renal mass will be determined by a survey provided to participants at a preoperative visit prior to surgery and at the 12-month follow-up visit.
Contact information is provided by the study sponsor or research team.
Case Comprehensive Cancer Center
Other
Oncologic, Functional and Surgical Outcomes for Patients Undergoing Radical Nephrectomy for Low-Risk Renal Cell Carcinoma and Recipients of Reconstructed Renal Allografts Following Ex-Vivo Partial Nephrectomy
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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