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Study of Tacrolimus Used for Pediatric Patients With Nephrotic Syndrome Based on Pharmacogenomics and Metabonomics

Primary Purpose

Nephrotic Syndrome

Status
Unknown status
Phase
Locations
China
Study Type
Observational
Intervention
therapeutic drug monitoring
Sponsored by
Guangzhou Women and Children's Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an observational trial for Nephrotic Syndrome

Eligibility Criteria

1 Month - 14 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. patients with refractory nephrotic syndrome;
  2. patients age ≤14y.

Exclusion Criteria:

  1. patients are sensitive to steroid;
  2. combined therapy with other immunosuppressive agent;
  3. combined using drugs which maybe interact the concentration of tacrolimus;
  4. with other malignant disease, such as tumor.

Sites / Locations

  • Guangzhou women and children's medical center

Arms of the Study

Arm 1

Arm 2

Arm Type

Arm Label

good efficacy

poor efficacy

Arm Description

using therapeutic drug monitoring to adjust the dose of tacrolimus. patients can reach effective outcome.

using therapeutic drug monitoring to adjust the dose of tacrolimus. patients can not reach effective outcome.

Outcomes

Primary Outcome Measures

"Genotypes as measured by polymerase chain reaction-restriction fragment length polymorphism"
genotype are collected from hospital system.
"Concentration as measured by liquid chromatography mass spectrometry"
concentration of tacrolimus are collected from hospital system.
"Relationship between genotypes and concentration as analyzed at 1 week"
using Statistic Package for Social Science 21.0 software to analyze the relationship between gene polymorphism and concentration.

Secondary Outcome Measures

Full Information

First Posted
September 9, 2015
Last Updated
August 11, 2016
Sponsor
Guangzhou Women and Children's Medical Center
Collaborators
Sun Yat-sen University
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1. Study Identification

Unique Protocol Identification Number
NCT02602873
Brief Title
Study of Tacrolimus Used for Pediatric Patients With Nephrotic Syndrome Based on Pharmacogenomics and Metabonomics
Official Title
Guangzhou Women and Children's Medical Center
Study Type
Observational

2. Study Status

Record Verification Date
August 2016
Overall Recruitment Status
Unknown status
Study Start Date
August 2015 (undefined)
Primary Completion Date
July 2017 (Anticipated)
Study Completion Date
August 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Guangzhou Women and Children's Medical Center
Collaborators
Sun Yat-sen University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Tacrolimus is recommended to be the first line therapeutic medication within the several immunosuppressive agents when treating refractory pediatric nephrotic syndrome, because of its definite efficacy and low toxicity. But there are still some key problems which hinder the using of tacrolimus in clinic, such as its narrow therapeutic widow, great individual difference of pharmacokinetics. Routine therapeutic drug monitoring(TDM) is needed in practice. But the disadvantage of TDM is hysteresis, which could lead to treatment failure or toxicity. To find out the reasons of great pharmacokinetic difference between patients and find out the individual proper dosage before administration are important for the clinical using of tacrolimus. It is hot in research of tacrolimus in organ transplant field, such as the association between gene polymorphisms of cytochrome P-450 3A4, 3A5 and multiple drug resistant gene(MDR1) and concentration of tacrolimus. However, there is few study about pharmacogenomics and metabonomics of tacrolimus in patients of nephrotic syndrome. The aim is to study the relationships between pharmacogenomics, metabonomics of tacrolimus and its efficacy, toxicity and blood concentration in patients of nephrotic syndrome, to find out the exact dosage before administration, to provide reference to individual drug administration.
Detailed Description
Investigators will collect data about efficacy and adverse drug reaction(ADR) such as time of efficacy when evaluated, how to evaluate ADR, data of demography, etc.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nephrotic Syndrome

7. Study Design

Enrollment
150 (Anticipated)
Biospecimen Retention
Samples With DNA
Biospecimen Description
DNAs extracted from whole blood are stored in freezer with -80 centigrade.

8. Arms, Groups, and Interventions

Arm Title
good efficacy
Arm Description
using therapeutic drug monitoring to adjust the dose of tacrolimus. patients can reach effective outcome.
Arm Title
poor efficacy
Arm Description
using therapeutic drug monitoring to adjust the dose of tacrolimus. patients can not reach effective outcome.
Intervention Type
Other
Intervention Name(s)
therapeutic drug monitoring
Intervention Description
with therapeutic drug monitoring , dose of tacrolimus can be adjusted by therapeutic drug monitoring.
Primary Outcome Measure Information:
Title
"Genotypes as measured by polymerase chain reaction-restriction fragment length polymorphism"
Description
genotype are collected from hospital system.
Time Frame
1 week
Title
"Concentration as measured by liquid chromatography mass spectrometry"
Description
concentration of tacrolimus are collected from hospital system.
Time Frame
1 week
Title
"Relationship between genotypes and concentration as analyzed at 1 week"
Description
using Statistic Package for Social Science 21.0 software to analyze the relationship between gene polymorphism and concentration.
Time Frame
1 week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Month
Maximum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients with refractory nephrotic syndrome; patients age ≤14y. Exclusion Criteria: patients are sensitive to steroid; combined therapy with other immunosuppressive agent; combined using drugs which maybe interact the concentration of tacrolimus; with other malignant disease, such as tumor.
Study Population Description
pediatric patients with nephrotic syndrome
Sampling Method
Non-Probability Sample
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Min Huang, Doctor
Organizational Affiliation
Sun Yat-sen University
Official's Role
Study Director
Facility Information:
Facility Name
Guangzhou women and children's medical center
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510623
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
we are carrying out experiment now. Data is not ready to publish for not completing the study. We will share data when we complete our study.
Citations:
PubMed Identifier
31902946
Citation
Mo X, Li J, Liu Y, Liao X, Tan M, Chen Y, He F, He Y, Li Y, Huang M. Kidney podocyte-associated gene polymorphisms affect tacrolimus concentration in pediatric patients with refractory nephrotic syndrome. Pharmacogenomics J. 2020 Aug;20(4):543-552. doi: 10.1038/s41397-019-0141-x. Epub 2020 Jan 6.
Results Reference
derived

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Study of Tacrolimus Used for Pediatric Patients With Nephrotic Syndrome Based on Pharmacogenomics and Metabonomics

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