A Clinical Study of the Living Renal Transplantation With Restored Kidneys Between Family Members

Not Applicable

• Conditions: Kidney Neoplasm; Kidney Stone; Ureteral Tumor; Ureteral Stricture; Renal Insufficiency

• Registration Number: NCT00994188
• Lead Sponsor: Tokushukai Medical Group

Brief Summary

Approximately 30,000 new patients are introduced into dialysis and about 20,000 of them die every year in Japan. At present, about 300,000 patients are on dialysis and more than 10,000 patients are registered with the Japan Organ Transplant Network (JOTN) with the hope for a renal transplantation. If the renal function is restored by transplantation, the quality of life (QOL) improves and more than 90% are reportedly comeback to their normal life activities and get relieved from the burden of dialysis. Furthermore, it can reduce the dialysis related medical cost by as much as 50%. However, only about 1,000 renal transplantation cases are annually carried out in Japan. Among them, 80-85% are living renal transplantations offered by family members or relatives, and the rest are from deceased donors.

Due to the fact that the number of deceased donors are scarce and only living renal transplantations between the family members or relatives are currently allowed in Japan, the approximate waiting time to receive a renal transplantation is 16 years. For that reason, many patients travel abroad to receive a renal transplantation.

There are reports that total nephrectomies are performed as a treatment for small size (4 cm or less) renal tumors, renal stones, ureteral tumors and ureteral strictures in many cases and that many of these nephrectomized kidneys can be successfully transplanted after surgical restoration with satisfactory results. However, due to the lack of necessary evidence it is currently not allowed in Japan.

Therefore, the investigators planned the present clinical study to evaluate the curative efficacy (renal function, QOL) and safety (side effects, complications or occurrence of renal cancer) of living renal transplantations between family members and relatives with restored donor kidneys after the surgical removal or repairment of a small size (4 cm or less) renal tumor or renal stone, ureteral tumor or ureteral stricture, in order to acquire necessary clinical data for potential enrichment of the renal donor pool in Japan as well as to develop useful medical care for our patients who are on dialysis for many years due to the renal failure.

Detailed Description

Not available

Study Timeline

• Study Start: 2009-07
• Status Verified: 2009-10
• Study First Submitted: 2009-10-09
• Study First Submitted QC: 2009-10-13
• Last Update Submitted: 2009-10-13
• Study First Posted: 2009-10-14
• Last Update Posted: 2009-10-14
• Primary Completion: 2014-06
• Study Completion: 2014-06

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 5

Inclusion Criteria

A) Recipient:

• Patients who are suffering from renal failure and are willing to receive a restored kidney from a family member
• Patients who are eligible for general anesthesia
• Patients who have given written informed consent to participate in the study

B) Donor:

• Potential donors who are incidentally diagnosed with small renal tumor (size: <4 cm) or renal stone, ureteral tumor or ureteral stricture and have permitted to transplant the kidney to a family member upon its surgical restoration
• Patients who are eligible for general anesthesia
• Patients who have given written informed consent to participate in the study

Exclusion Criteria

A) Recipient:

• Patients who have infectious disease, hemorrhagic ulcer, or malignant cancer
• Patients who have serious vascular lesions (eg. arteriosclerosis, thromboembolic disease) and are currently on treatment
• Patients who were disapproved by the Institutional Ethics Committee

B) Donor:

• Patients who have tested positive for serious infectious disease (eg. HIV, HBV, or HCV)
• Patients who were diagnosed with malignant lymphoma or sarcoma
• Patients who were on chemotherapy or radiation therapy for renal cancer prior to the nephrectomy
• Patients who were disapproved by the Institutional Ethics Committee

(*) Other inclusion/exclusion criteria defined in the protocol for both recipient and donor may apply.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Evaluation of curative efficacy (renal function and QOL) and safety (side effects, complications) after renal transplantation with restored kidneys between family members	12 Months

Trial Locations

Locations (2)

Tokyo-West Tokushukai Hospital Transplant Office; 🇯🇵 Akishima City, Tokyo, Japan

Uwajima Tokushukai Hospital; 🇯🇵 Uwajima, Ehime, Japan