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UnknownNCT01513707

The Effects of Pre-transplant Dialysis Modality on Post-transplant Events

Status
Unknown
Phase
Study type
Observational
Enrollment
1,040 (estimated)
Sponsor
Ha Young Oh · Academic / Other
Sex
All
Age
20 Years – 70 Years
Healthy volunteers
Not accepted

Summary

This is a prospective, multicenter, comparative, parallel-group, observational study. There will be 2 cohorts according to pre-transplant dialysis modality (hemodialysis or peritoneal dialysis). In each cohort, subjects will be observed for 12 months. Approximately, 1040 subjects will be enrolled from 8 transplant centers. Subjects will be enrolled consecutively until the number of subjects in peritoneal dialysis group has been 260. It will take 2 years. In this period, the number of subject in hemodialysis group enrolled in this study will be 780. After finishing the observation of all subjects, to balance clinical and demographic baseline characteristics between the two groups, subjects will be selected in each cohort with 1:1 matched using propensity score method. And then primary and secondary endpoints will be compared between two groups.

Detailed description

1\. STUDY OBJECTIVES AND ENDPOINTS 1.1. Objectives The primary objective of this study is: • To compare the incidence of composite outcomes (delayed graft function, functional delayed graft function, primary nonfunction, biopsy-proven acute rejection) of pre-transplant dialysis modality hemodialysis versus peritoneal in recipients of first renal allografts at 1 year posttransplant. The secondary objectives of this study are: * To compare the incidence of delayed graft function and functional delayed graft function of pre-transplant dialysis modality hemodialysis versus peritoneal in recipients of first renal allografts at 1 year posttransplant; * To compare the incidence of composite outcomes biopsy-proven acute rejection of pre-transplant dialysis modality hemodialysis versus peritoneal in recipients of first renal allografts at 1 year posttransplant; * To compare the incidence of primary nonfunction of pre-transplant dialysis modality hemodialysis versus peritoneal in recipients of first renal allografts at 1 year posttransplant; * To evaluate the effect of hemodialysis or peritoneal dialysis on graft function in terms of longitudinal change of eGFR calculated with abbreviated MDRD equation at Weeks 8, 16, 24, 32, 40, and 48 after renal transplant; * To compare the incidence and the duration of hospitalization after kidney transplantation of pre-transplant dialysis modality hemodialysis versus peritoneal in recipients of first renal allografts at 1 year posttransplant; * To compare the graft loss and subject death rate of pre-transplant dialysis modality hemodialysis versus peritoneal in recipients of first renal allografts at 1 year posttransplant. 1.2. Endpoints Primary endpoint: * Composite outcome including; 1. Delayed graft function (defined as the need for dialysis in the first week after transplantation) 2. Functional DGF (defined as the absence of a decrease in serum creatinine level by a minimum of 10% per day during 3 consecutive days in the first postoperative week, not including patients in whom acute rejection, calcineurin inhibitor toxicity, or both, developed within the first week 3. Primary nonfunction (defined as the kidney never achieving function after transplantation) 4. Biopsy proven acute rejection (defined as scute rejection, confirmed by allograft biopsy) Secondary endpoints: * eGFR (calculated with abbreviated MDRD equation at Weeks 8, 16, 24, 32, 40 and 48 after renal transplant) * Hospitalization after kidney transplant (any cause, duration) * Delayed graft function, functional DGF, Primary nonfunction, biopsy proven acute rejection (definition of each endpoint is described above) * Graft loss (return to long-term dialysis) * Subject death (any cause)

Conditions

Timeline

Start date
2011-12-22
Primary completion
2017-09-01
Completion
2017-12-01
First posted
2012-01-20
Last updated
2017-04-27

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01513707. Inclusion in this directory is not an endorsement.