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Efficacy of Yinzhihuang Oral Liquid on Indirect Bilirubin of Neonates With Glucose-6-phosphate Dehydrogenase Deficiency

Primary Purpose

Neonatal Hyperbilirubinemia

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Yinzhihuang Oral Liquid
Sponsored by
Southern Medical University, China
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neonatal Hyperbilirubinemia focused on measuring G6PD Deficiency, Neonatal Hyperbilirubinemia, Yinzhihuang Oral Liquid, Indirect Bilirubin

Eligibility Criteria

3 Days - 7 Days (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Full-term newborns with jaundice after 3-7 days of birth, total bilirubin in serum or transcutaneous bilirubin is between 100umol/L and 257umol/L, and start taking Yinzhihuang oral liquid, dose: 3ml per each time, 3 times per each day, during the period, measuring bilirubin from skin one time every 24 hours;
  2. Gestational age≥37 weeks, birth weight≥2.5Kg, Apgar scores≥8;
  3. lineal consanguinity are all the native residents from Guangdong or Guangxi;
  4. The enzyme activity of G-6-PD will be detected and collected from all the neonates subjects;
  5. Informed consents of all the neonates subjects are needed.

Note: Icterus testers are Minolta 105 type. Measurements of bilirubin are from three location, inluding forehead, chest and abdomen. The value of bilirubin will use the average value from the three location, and the unit is umol / L.

Exclusion Criteria:

  1. Neonates with inherited metabolic diseases;
  2. Neonates with congenital malformation of liver and gallbladder;
  3. Neonates with asphyxia, hypoxia, acidosis, sepsis, high fever, low temperature, low protein, low blood sugar, etc. which may lead to bilirubin encephalopathy;
  4. History of oxidation drug exposure(e.g. honeysuckle bath)

Sites / Locations

  • The South Hospital of Southern Medical UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

G-6-PD normal group

G-6-PD mild deficiency group

G-6-PD moderate deficiency group

G-6-PD sever deficiency group

Arm Description

Drug: Yinzhihuang Oral Liquid, dose: 3ml each time, 3 times every day, during the period, measuring bilirubin from skin one time every 24 hours.

Drug: Yinzhihuang Oral Liquid, dose: 3ml each time, 3 times every day, during the period, measuring bilirubin from skin one time every 24 hours.

Drug: Yinzhihuang Oral Liquid, dose: 3ml each time, 3 times every day, during the period, measuring bilirubin from skin one time every 24 hours.

Drug: Yinzhihuang Oral Liquid, dose: 3ml each time, 3 times every day, during the period, measuring bilirubin from skin one time every 24 hours.

Outcomes

Primary Outcome Measures

The change(umol/L) from baseline of total bilirubin(umol/L) will be calculated and finalized
Value of the total bilirubin in serum(umol/L) will be collected and calculated.

Secondary Outcome Measures

The percent change(%) from baseline of total bilirubin(umol/L) will be calculated and finalized
Value of the total bilirubin in serum(umol/L) will be collected and calculated.

Full Information

First Posted
October 28, 2015
Last Updated
October 31, 2015
Sponsor
Southern Medical University, China
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1. Study Identification

Unique Protocol Identification Number
NCT02594904
Brief Title
Efficacy of Yinzhihuang Oral Liquid on Indirect Bilirubin of Neonates With Glucose-6-phosphate Dehydrogenase Deficiency
Official Title
A Multicenter Study to Evaluate the Efficacy of Yinzhihuang Oral Liquid on Indirect Bilirubin of Neonates With Glucose-6-phosphate Dehydrogenase Deficiency
Study Type
Interventional

2. Study Status

Record Verification Date
October 2015
Overall Recruitment Status
Unknown status
Study Start Date
July 2015 (undefined)
Primary Completion Date
April 2016 (Anticipated)
Study Completion Date
June 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Southern Medical University, China

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Neonatal Glucose-6-phosphate Dehydrogenase(G6PD) Deficiency is one of the significant reason for neonatal hyperbilirubinemia and even irreversible bilirubin encephalopathy.The neonates may be attacked due to acute infection, eating beans or exposure to oxidative drugs, etc. The main clinical manifestations are hemolytic anemia, and the resulting hyperbilirubinemia. When bilirubin is pretty high in body, bilirubin may spread into brain, and thus cause nervous system damage, and severely affect the prognosis of neonates. Therefore, monitoring and early intervention of jaundice has important significance to prevent further aggravation of jaundice and certain sequelae. Phototherapy and exchange transfusion are mainly suitable methods for severe hyperbilirubinemia, however, patients need to be hospitalized. Yinzhihuang Oral Liquid is a kind of traditional Chinese medicine for jaundice. Many large sample and multicenter clinical studies show that the positive efficacy of Yinzhihuang Oral Liquid in the treatment of neonatal hyperbilirubinemia is exactly confirmed. The purpose of this study is try to detect the treatment effect of Yinzhihuang Oral Liquid on indirect bilirubin in neonates with G-6-PD enzyme deficiency and neonatal hyperbilirubinemia. Try to provide scientific theories for Yinzhihuang Oral Liquid to treat neonates with G-6-PD enzyme deficiency and neonatal hyperbilirubinemia.
Detailed Description
The primary objective is to detect the treatment effect of Yinzhihuang Oral Liquid on indirect bilirubin in neonates with G-6-PD enzyme deficiency and neonatal hyperbilirubinemia. Try to provide scientific theories for Yinzhihuang Oral Liquid to treat neonates with G-6-PD enzyme deficiency and neonatal hyperbilirubinemia. Study subjects includes neonates with hyperbilirubinemia from five hospitals, who are willing to take Yinzhihuang oral liquid. Five hospitals are South Hospital of Southern Medical University (primary institute), The Third Affiliated Hospital of Guangzhou medical university, Shenzhen maternal and child health hospital, First Affiliated Hospital of Guangxi Medical University, The maternal and child health hospital of Guangxi Zhuang Autonomous Region Inclusion criteria: Full-term newborns with jaundice after 3-7 days of birth, total bilirubin in serum or transcutaneous bilirubin is between 100umol/L and 257umol/L, and start taking Yinzhihuang oral liquid, dose: 3ml per each time, 3 times per each day, during the period, measuring bilirubin from skin one time every 24 hours; Gestational age≥37 weeks, birth weight≥2.5Kg, Apgar scores≥8; lineal consanguinity are all the native residents from Guangdong or Guangxi; The enzyme activity of G-6-PD will be detected and collected from all the neonates subjects; Informed consents of all the neonates subjects are needed. Exclusion Criteria: (1) Neonates with inherited metabolic diseases; (2) Neonates with congenital malformation of liver and gallbladder; (3) Neonates with asphyxia, hypoxia, acidosis, sepsis, high fever, low temperature, low protein, low blood sugar, etc. which may lead to bilirubin encephalopathy; (4)History of oxidation drug exposure(e.g. honeysuckle bath) Study procedures: Outpatient and inpatient neonates (mainly for cesarean section newborns), with jaundice after 3-7 days of birth, total bilirubin in serum or measuring bilirubin from skin is between 100umol/L and 257umol/L, will be selected. On the first day of jaundice, the G-6-PD enzyme activity will be detected by checking arterial blood, and then start taking Yinzhihuang oral liquid, dose: 3ml each time, 3 times every day, during the period, measuring bilirubin from skin one time every 24 hours. When the transcutaneous bilirubin is below 100umol/L, stop taking the medication. When bilirubin increases to match the phototherapy indications, the neonates will be transferred to the neonatal department, and continue the Yinzhihuang oral liquid treatment until bilirubin decreasing to normal level. after the transfer to the ICU still needs to continue to use until the jaundice decreased to normal level. The neonates 's families have to sign the informed consents before entering the study. G-6-PD <10.37U /g.H b was diagnosed as a lack of G-6-PD activity. Subgroup: according to the severity of the lack of the activity of the enzyme, it will be divided into 3 groups: mild deficiency: 6.93-10.37U/g.H b; moderate deficiency: 3.47-6.92U/g. Hb; severe deficiency: 0-3.46U/g.H b. Note: the above criteria can be modified according to the test methods of those five hospitals, and will be uniformed by same final standards. The normal value of G-6-PD enzyme activity is 2.5-5.8KU/L in our hospital, <2.5KU/L can be diagnosed as lack of G-6-PD enzyme activity. However, there is no certain standards for the definition of mild deficiency, moderate deficiency and severe deficiency in our hospital. It was reported that activity is less than 10% of normal is severe deficiency, less than 10%-60% of normal is moderate deficiency, less than 60% of normal is mild deficiency.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neonatal Hyperbilirubinemia
Keywords
G6PD Deficiency, Neonatal Hyperbilirubinemia, Yinzhihuang Oral Liquid, Indirect Bilirubin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
G-6-PD normal group
Arm Type
Experimental
Arm Description
Drug: Yinzhihuang Oral Liquid, dose: 3ml each time, 3 times every day, during the period, measuring bilirubin from skin one time every 24 hours.
Arm Title
G-6-PD mild deficiency group
Arm Type
Experimental
Arm Description
Drug: Yinzhihuang Oral Liquid, dose: 3ml each time, 3 times every day, during the period, measuring bilirubin from skin one time every 24 hours.
Arm Title
G-6-PD moderate deficiency group
Arm Type
Experimental
Arm Description
Drug: Yinzhihuang Oral Liquid, dose: 3ml each time, 3 times every day, during the period, measuring bilirubin from skin one time every 24 hours.
Arm Title
G-6-PD sever deficiency group
Arm Type
Experimental
Arm Description
Drug: Yinzhihuang Oral Liquid, dose: 3ml each time, 3 times every day, during the period, measuring bilirubin from skin one time every 24 hours.
Intervention Type
Drug
Intervention Name(s)
Yinzhihuang Oral Liquid
Other Intervention Name(s)
Huarun Yinzhihuang Oral solution
Intervention Description
All the four groups will be given same treatment as being described in arm description.
Primary Outcome Measure Information:
Title
The change(umol/L) from baseline of total bilirubin(umol/L) will be calculated and finalized
Description
Value of the total bilirubin in serum(umol/L) will be collected and calculated.
Time Frame
Every 24 hours during dosing, for around three days.(Typicall the dosing will be stopped once the bilirubin is below 100umol/L)
Secondary Outcome Measure Information:
Title
The percent change(%) from baseline of total bilirubin(umol/L) will be calculated and finalized
Description
Value of the total bilirubin in serum(umol/L) will be collected and calculated.
Time Frame
Every 24 hours during dosing, for around three days.(Typicall the dosing will be stopped once the bilirubin is below 100umol/L)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Days
Maximum Age & Unit of Time
7 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Full-term newborns with jaundice after 3-7 days of birth, total bilirubin in serum or transcutaneous bilirubin is between 100umol/L and 257umol/L, and start taking Yinzhihuang oral liquid, dose: 3ml per each time, 3 times per each day, during the period, measuring bilirubin from skin one time every 24 hours; Gestational age≥37 weeks, birth weight≥2.5Kg, Apgar scores≥8; lineal consanguinity are all the native residents from Guangdong or Guangxi; The enzyme activity of G-6-PD will be detected and collected from all the neonates subjects; Informed consents of all the neonates subjects are needed. Note: Icterus testers are Minolta 105 type. Measurements of bilirubin are from three location, inluding forehead, chest and abdomen. The value of bilirubin will use the average value from the three location, and the unit is umol / L. Exclusion Criteria: Neonates with inherited metabolic diseases; Neonates with congenital malformation of liver and gallbladder; Neonates with asphyxia, hypoxia, acidosis, sepsis, high fever, low temperature, low protein, low blood sugar, etc. which may lead to bilirubin encephalopathy; History of oxidation drug exposure(e.g. honeysuckle bath)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Weimin Huang, Ph.D
Phone
+8613900261113
Email
drhwm2003@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Weimin Huang, Ph.D
Organizational Affiliation
The South Hospital of Southern Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The South Hospital of Southern Medical University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510515
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Weimin Huang, Ph.D
Phone
13900261113
Email
drhwm2003@hotmail.com

12. IPD Sharing Statement

Citations:
PubMed Identifier
19942489
Citation
Kaplan M, Hammerman C. Glucose-6-phosphate dehydrogenase deficiency and severe neonatal hyperbilirubinemia: a complexity of interactions between genes and environment. Semin Fetal Neonatal Med. 2010 Jun;15(3):148-56. doi: 10.1016/j.siny.2009.10.007. Epub 2009 Nov 26.
Results Reference
background
PubMed Identifier
19233695
Citation
Nkhoma ET, Poole C, Vannappagari V, Hall SA, Beutler E. The global prevalence of glucose-6-phosphate dehydrogenase deficiency: a systematic review and meta-analysis. Blood Cells Mol Dis. 2009 May-Jun;42(3):267-78. doi: 10.1016/j.bcmd.2008.12.005. Epub 2009 Feb 23.
Results Reference
background
PubMed Identifier
22176900
Citation
Clinical Research Collaborative Group of Yinzhihuang Oral Solution. [A multicenter randomized controlled study on the efficacy and safety of Yinzhihuang oral solution for the treatment of neonatal indirect hyperbilirubinemia in term newborn infants]. Zhonghua Er Ke Za Zhi. 2011 Sep;49(9):663-8. Chinese.
Results Reference
background

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Efficacy of Yinzhihuang Oral Liquid on Indirect Bilirubin of Neonates With Glucose-6-phosphate Dehydrogenase Deficiency

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