A Clinical Study of the Living Renal Transplantation With Restored Kidneys Between Third Parties

Sponsor

Tokushukai Medical Group (Other)

Overall Status

Unknown status

CT.gov ID

NCT00980317

Collaborator

(none)

Enrollment

Locations

Duration (Months)

2.5

Patients Per Site

Patients Per Site Per Month

Study Details

Study Description

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 to 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 come back 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 renal transplantations between non-relatives (third parties) are currently not 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 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 occurence of renal cancer) of living renal transplantations between third parties (non-relatives) with restored donor kidneys after the surgical removal of a small size (4 cm or less) renal tumor, 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.

Condition or Disease	Intervention/Treatment	Phase
Kidney Neoplasms Renal Insufficiency Renal Replacement Therapy	Procedure: Restored Kidney Transplant Between Third Parties	N/A

Study Design

Study Type:

Interventional

Anticipated Enrollment :

5 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

A Clinical Study of the Living-unrelated Renal Transplantation With Restored Kidneys (Interventional Trial)

Study Start Date :

Jul 1, 2009

Anticipated Primary Completion Date :

Jun 1, 2014

Anticipated Study Completion Date :

Jun 1, 2014

Outcome Measures

Primary Outcome Measures

Evaluation of curative efficacy (renal function and QOL) and safety (side effects, complications or occurence of renal cancer) after renal transplantation with restored donor kidneys to third party recipients [12 Months]

Eligibility Criteria

Criteria

Ages Eligible for Study:

20 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Recipient:

Patients who are on dialysis and are willing to receive a restored kidney from a third party
Patients who are eligible for general anesthesia
Patients who have given written informed consent to participate in the study

Donor:

Patients who have small tumor (size: <4 cm) in the kidney and have chosen total nephrectomy among all the available treatment options and have permitted to transplant the nephrectomized kidney to a third party 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:

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

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.