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NCT00903578 Clinical Trial

Impact of Fibroblast Growth Factor 23 (FGF-23) and Serum Phosphate on Allograft Function and Mortality in Kidney Allograft Recipients

Kidney Transplantation Clinical Trial

Official title:
Impact of FGF-23 and Serum Phosphate on Allograft Function and Mortality in Kidney Allograft Recipients

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT00903578
Other study ID # KT-1
Secondary ID
Status Active, not recruiting
Phase N/A
First received May 1, 2009
Last updated December 16, 2009
Start date May 2009
Est. completion date January 2015

Study information
Verified date December 2009
Source Ramathibodi Hospital
Contact n/a
Is FDA regulated No
Health authority Thailand: Ethical Committee
Study type Observational

Clinical Trial Summary

The present study will examine whether serum FGF-23 and serum phosphate at baseline of kidney transplant recipients can predict progression of allograft dysfunction at 3 years and all-cause mortality at 5 years.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 200
Est. completion date January 2015
Est. primary completion date January 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- at least one year post-transplantation

- no more than 10% increase in serum creatinine for the past 3 months

Exclusion Criteria:

- refuse to participate in the study

- any acute illnesses

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Thailand Ramathibodi Hospital, Mahidol University Phayathai Bangkok

Sponsors (1)
Lead Sponsor Collaborator
Ramathibodi Hospital

Country where clinical trial is conducted

Thailand, 

Outcome
Type Measure Description Time frame Safety issue
Primary Progression of allograft dysfunction and all-cause Mortality 3 and 5 years No
Secondary Relationship of FGF-23 and 25-OH-D, 1-25-OH-D, PTH, calcium, phosphate, urine phosphate and eGFR 1 year No
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