Colla Corii Asini Treating Anemia in Pregnant Women With Thalassemia(Presenting the Syndrome of Blood Deficiency)
Primary Purpose
Thalassemia
Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Colla corii asini
a Simulate Agent of Colla corii asini granule
Sponsored by
About this trial
This is an interventional treatment trial for Thalassemia focused on measuring Thalassemia;, the Syndrome of Blood Deficiency, Anemia, Colla Corii Asini
Eligibility Criteria
Inclusion Criteria:
- Pregnant women diagnosed as thalassemia carriers by genetic test with clinical presentation of silent or standard α-thalassemia, HbH disease, minor or intermediate β-thalassemia;
- Patients with mild anemia (70 g/L≤ Hb<100 g/L) prior to study enrollment;
- Singleton pregnancy ;
- Gestational age between 24-32 weeks;
- Patients having not received blood transfusion in the last 12 weeks;
- Written informed consent of the patient.
Exclusion Criteria:
- Known history of allergy or reaction to any component of the investigational product;
- Allergic to two or more drugs;
- Patients with severe thalassemia;
- Anaemia not caused by thalassemia (e.g., iron deficiency, aplastic, megaloblastic or haemolytic anaemia) or bone marrow diseases, leukemia.
- Twin or multiple pregnancies;
- Placental Abnormality (e.g., placenta previa, multilobate placenta, placenta succenturiate, placenta cirumvallate) or polyhydramnios, oligohydramnios, fetal growth restriction, fetal anomaly;
- Patients having received hemopoieticfactors or treated by hematopoietic stem cell transplantation in the last 2 months;
- Hypersplenism or hypertensive disorder in pregnancy;
- Patients with any of the following abnormalities: immunodeficiency, primary diseases involving cardiovascular system, liver, kidney, gastrointestinal tract, endocrine system and hematological system;
- 1.5 times or more higher plasma creatinine level than high limit of normal state;
- 1.5 times or more higher AST or ALT than high limit of normal state;
- Patients with mental illness;
- Patients who suffer from drug or alcohol abuse;
- Patients who addicted to smoking and drinking;
- Participation in any clinical investigational drug study within the previous 3 months;
- Patients who are regarded as ineligible for this study by investigator.
Sites / Locations
- The third people's Hospital of Dongguan
- Intranet of Guangzhou Women and Children's Medical CenterRecruiting
- the first affiliated hospital of Guangzhou University of Chinese MedicineRecruiting
- Department of Gynaecology and Obstetrics,Nanfang Hospital, Southern Medical UniversityRecruiting
- The First Affiliated Hospital of Jinan UniversityRecruiting
- The Fifth Affiliated Hospital of Guangzhou Medical UniversityRecruiting
- Dongguan Guangji Hospital
- Shenzhen maternity and child health care hospital
- Liuzhou Municipal Matemal and Child Health HospitalRecruiting
- The Guangxi Zhuang Autonomous Region National HospitalRecruiting
- Ruikang Hospital of Guangxi University of Traditional Chinese MedicineRecruiting
- The First Affiliated Hospital of Guangxi University of Chinese Medicine
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Experimental group
Control group
Arm Description
15g of Colla corii asini granule( produced by Dong-E E-Jiao Co., Ltd) , taken once daily for 8 weeks
a Simulate Agent of Colla corii asini granule, similar in size, shape,color and taste to Colla corii asini granule, taken once daily for 8 weeks
Outcomes
Primary Outcome Measures
Hemoglobin(Hb)
the change of hemoglobin(g/L)
Secondary Outcome Measures
reticulocyte (RET)
the change of reticulocyte (RET)count(×10^9/L)
immature reticulocyte fraction(IRF)
the change of immature reticulocyte fraction(%)
adverse event
undesirable pregnancy outcomes
indirect bilirubin(IBIL)
the change of indirect bilirubin(IBIL)(μmol/L)
total bilirubin(TBIL)
the change of total bilirubin(TBIL) (μmol/L)
lactic dehydrogenase(LDH)
the change of lactic dehydrogenase(LDH)(U/L)
anaemia cure rates
anaemia cure rates(%):The concentration of hemoglobin was higher than baseline > 5g/L;The improvement rate = improved cases/the total number of cases * 100%
The curative effect of TCM Syndrome
the change of the TCM syndrome scores of two groups before and after treatment(%)
Full Information
NCT ID
NCT03374111
First Posted
December 4, 2017
Last Updated
December 26, 2018
Sponsor
The First Affiliated Hospital, Guangzhou University of Traditional Chinese Medicine
1. Study Identification
Unique Protocol Identification Number
NCT03374111
Brief Title
Colla Corii Asini Treating Anemia in Pregnant Women With Thalassemia(Presenting the Syndrome of Blood Deficiency)
Official Title
A Multi-center Randomized, Double-blind, Placebo-controlled Study of Colla Corii Asini for the Treatment of Anemia in Pregnant Women With Thalassemia(Presenting the Syndrome of Blood Deficiency)
Study Type
Interventional
2. Study Status
Record Verification Date
December 2018
Overall Recruitment Status
Unknown status
Study Start Date
March 1, 2018 (Actual)
Primary Completion Date
October 1, 2019 (Anticipated)
Study Completion Date
December 30, 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The First Affiliated Hospital, Guangzhou University of Traditional Chinese Medicine
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
480 pregnant patients diagnosed of silent or standard α-thalassemia, HbH disease, minor or intermediate β-thalassemia with mild anemia will be randomly assigned to treatment group and control group. Patients in the treatment group will be given 15 g of Colla corii asini powder form daily for 8 weeks and followed up to 42 days postpartum while the control group will be observed and followed up in the same period treated with placebo. Levels of hemoglobin(Hb), reticulocyte (RET), immaturity reticulocyte (IRF), indirect bilirubin(IBIL), total bilirubin(TBIL), lactic dehydrogenase(LDH) will be measured on three visits(baseline, week 4 and week 8). The curative effect of TCM Syndrome( week 8) and undesirable pregnancy outcomes(42 days after giving birth) will be observed.
Detailed Description
Thalassemia is a type of hemolytic anemia disease caused by genetic defect of synthesis in one or more globin chains. Among all the single genetic disorders thalassemia has the highest incidence rate in the world and causes heavy burdens on public health system. In China, the southern provinces suffer from high incidence of thalassemia, which is particularly common in the population of Guangdong, Guangxi and Yunnan provinces. Epidemiological studies showed that in Guangdong alone about 17.83 % of the 14,332 pregnant women across 21 regions examined were diagnosed as carriers of thalassemia .
Recent studies showed that compared with healthy controls, women with thalassemia are associated with a wide range of abnormality and adverse pregnancy outcomes including cardiovascular disease, thrombotic disease, spontaneous miscarriage, premature delivery, oligohydramnios, fetal growth restriction and low birth weight. Currently there is no consensus on treating anemia in pregnant thalassemia patients. Due to the absence of an safe and effective therapeutic measures, many thalassemia patients are prone to develop low level of Hb, which can severely impact the fetal growth and maternal health.
In traditional Chinese medicine (TCM), Colla corii asini (CCA, E'jiao) is a gelatin-like traditional Chinese medicine refined from donkey hide and has been widely used in clinical antanemic therapy for more than 2000 years. In the last decade, many studies had addressed the effect of CCA on the anemia using modern pharmacological approaches. The results indicated that CCA contains collagen protein,glycogen and a variety of trace elements, a variety of amino acids, etc. the main components of CCA can promote hematopoiesis by a number of mechanisms which eventually increase the peripheral erythrocyte counts and Hb concentration. Therefore, the investigators proposed that the hematopoietic effects of CCA might also contribute to the treatment of thalassemia with insuffcient or abnormal Hb concentration.
The study aims to evaluate the efficacy and safety of Colla corii asini (CCA ) in improve anemia during pregnancy among silent or standard α-thalassemia, HbH disease, minor or intermediate β-thalassemia. Four hundred and eighty pregnant patients who meet inclusion criteria will be randomly assigned to either the treatment group or control group. Patients in the treatment group will be given 15 g of CCA daily for 8 weeks and followed up to 42 days postpartum, while the control group were observed and followed up in the same period treated with placebo. Levels of hemoglobin (Hb),reticulocyte (RET), immaturity reticulocyte (IRF), indirect bilirubin (IBIL), total bilirubin (TBIL), lactic dehydrogenase (LDH) will be measured on three visits (baseline, week 4 and week 8). The curative effect of TCM Syndrome( week 8) and undesirable pregnancy outcomes(42 days after giving birth) will be observed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Thalassemia
Keywords
Thalassemia;, the Syndrome of Blood Deficiency, Anemia, Colla Corii Asini
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
double blind
Allocation
Randomized
Enrollment
480 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Experimental group
Arm Type
Experimental
Arm Description
15g of Colla corii asini granule( produced by Dong-E E-Jiao Co., Ltd) , taken once daily for 8 weeks
Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
a Simulate Agent of Colla corii asini granule, similar in size, shape,color and taste to Colla corii asini granule, taken once daily for 8 weeks
Intervention Type
Drug
Intervention Name(s)
Colla corii asini
Other Intervention Name(s)
donkey-hide gelatin
Intervention Description
15 g Colla corii asini granule daily for 8 weeks
Intervention Type
Drug
Intervention Name(s)
a Simulate Agent of Colla corii asini granule
Other Intervention Name(s)
Placebo of Colla corii asini granule
Intervention Description
15 g a Simulate Agent of Colla corii asini granule daily for 8 weeks
Primary Outcome Measure Information:
Title
Hemoglobin(Hb)
Description
the change of hemoglobin(g/L)
Time Frame
baseline, week 4 and week 8
Secondary Outcome Measure Information:
Title
reticulocyte (RET)
Description
the change of reticulocyte (RET)count(×10^9/L)
Time Frame
baseline, week 4 and week 8
Title
immature reticulocyte fraction(IRF)
Description
the change of immature reticulocyte fraction(%)
Time Frame
baseline, week 4 and week 8
Title
adverse event
Description
undesirable pregnancy outcomes
Time Frame
tracked for 42 days after giving birth
Title
indirect bilirubin(IBIL)
Description
the change of indirect bilirubin(IBIL)(μmol/L)
Time Frame
baseline, week 4 and week 8
Title
total bilirubin(TBIL)
Description
the change of total bilirubin(TBIL) (μmol/L)
Time Frame
baseline, week 4 and week 8
Title
lactic dehydrogenase(LDH)
Description
the change of lactic dehydrogenase(LDH)(U/L)
Time Frame
baseline, week 4 and week 8
Title
anaemia cure rates
Description
anaemia cure rates(%):The concentration of hemoglobin was higher than baseline > 5g/L;The improvement rate = improved cases/the total number of cases * 100%
Time Frame
week 8
Title
The curative effect of TCM Syndrome
Description
the change of the TCM syndrome scores of two groups before and after treatment(%)
Time Frame
week 8
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Pregnant women diagnosed as thalassemia carriers by genetic test with clinical presentation of silent or standard α-thalassemia, HbH disease, minor or intermediate β-thalassemia;
Patients with mild anemia (70 g/L≤ Hb<100 g/L) prior to study enrollment;
Singleton pregnancy ;
Gestational age between 24-32 weeks;
Patients having not received blood transfusion in the last 12 weeks;
Written informed consent of the patient.
Exclusion Criteria:
Known history of allergy or reaction to any component of the investigational product;
Allergic to two or more drugs;
Patients with severe thalassemia;
Anaemia not caused by thalassemia (e.g., iron deficiency, aplastic, megaloblastic or haemolytic anaemia) or bone marrow diseases, leukemia.
Twin or multiple pregnancies;
Placental Abnormality (e.g., placenta previa, multilobate placenta, placenta succenturiate, placenta cirumvallate) or polyhydramnios, oligohydramnios, fetal growth restriction, fetal anomaly;
Patients having received hemopoieticfactors or treated by hematopoietic stem cell transplantation in the last 2 months;
Hypersplenism or hypertensive disorder in pregnancy;
Patients with any of the following abnormalities: immunodeficiency, primary diseases involving cardiovascular system, liver, kidney, gastrointestinal tract, endocrine system and hematological system;
1.5 times or more higher plasma creatinine level than high limit of normal state;
1.5 times or more higher AST or ALT than high limit of normal state;
Patients with mental illness;
Patients who suffer from drug or alcohol abuse;
Patients who addicted to smoking and drinking;
Participation in any clinical investigational drug study within the previous 3 months;
Patients who are regarded as ineligible for this study by investigator.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Song-ping Luo, PhD
Phone
13005156625
Email
songpingluo@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Zhongqi Yang, PhD
Phone
+86-20-36598909
Email
Yang_zhongqi@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yanfang Li, PhD
Organizational Affiliation
the first affiliated hospital of Guangzhou University of Chinese Medicine , Guangzhou
Official's Role
Principal Investigator
Facility Information:
Facility Name
The third people's Hospital of Dongguan
City
Dongguan
State/Province
Guangdong
ZIP/Postal Code
523326
Country
China
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lifang Mo
Phone
13669853882
Email
478974155@qq.com
Facility Name
Intranet of Guangzhou Women and Children's Medical Center
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510405
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
shaoying Wu, PhD
Phone
18902268157
Email
wushaoying@163.com
Facility Name
the first affiliated hospital of Guangzhou University of Chinese Medicine
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510405
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yanfang Li, PhD
Phone
+86-20-36598857
Email
gzyanfangli@hotmail.com
First Name & Middle Initial & Last Name & Degree
Song-ping Luo, professor
Phone
13005156625
Email
songpingluo@hotmail.com
Facility Name
Department of Gynaecology and Obstetrics,Nanfang Hospital, 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
Zhijian WANG
Facility Name
The First Affiliated Hospital of Jinan University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510630
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rui-man Li
Facility Name
The Fifth Affiliated Hospital of Guangzhou Medical University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510700
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Junzhao Qiu
Facility Name
Dongguan Guangji Hospital
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
523382
Country
China
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Caifang Wang
Phone
15817696003
Facility Name
Shenzhen maternity and child health care hospital
City
Shenzhen
State/Province
Guangdong
ZIP/Postal Code
518033
Country
China
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yan Ning
Facility Name
Liuzhou Municipal Matemal and Child Health Hospital
City
Liuzhou
State/Province
Guangxi
ZIP/Postal Code
545001
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yuanliu Wang
Facility Name
The Guangxi Zhuang Autonomous Region National Hospital
City
Nanning
State/Province
Guangxi
ZIP/Postal Code
530001
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ruo xue You
Facility Name
Ruikang Hospital of Guangxi University of Traditional Chinese Medicine
City
Nanning
State/Province
Guangxi
ZIP/Postal Code
530011
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xin QIN
Facility Name
The First Affiliated Hospital of Guangxi University of Chinese Medicine
City
Nanning
State/Province
Guangxi
ZIP/Postal Code
530023
Country
China
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yong-qin Zhang
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
all collected IPD, all IPD that underlie results in a publication
IPD Sharing Time Frame
starting in May 2020 when the study have been completed and publication of a clinical trial report.
IPD Sharing Access Criteria
the information collected about the study will be used to support other research in the future, and may be shared anonymously with other researchers,data will be freely available to anyone upon request.
Citations:
PubMed Identifier
27456464
Citation
Li Y, He H, Yang L, Li X, Li D, Luo S. Therapeutic effect of Colla corii asini on improving anemia and hemoglobin compositions in pregnant women with thalassemia. Int J Hematol. 2016 Nov;104(5):559-565. doi: 10.1007/s12185-016-2069-0. Epub 2016 Jul 25.
Results Reference
background
PubMed Identifier
26949404
Citation
Cheng YL, Zhang XH, Sun YW, Wang WJ, Fang SP, Wu ZK. Clinical Effect and Mechanism of Yisui Shengxue Granules in Thalassemia Patients with Mild, Moderate, or Severe Anemia. Evid Based Complement Alternat Med. 2016;2016:1713897. doi: 10.1155/2016/1713897. Epub 2016 Feb 2.
Results Reference
background
Learn more about this trial
Colla Corii Asini Treating Anemia in Pregnant Women With Thalassemia(Presenting the Syndrome of Blood Deficiency)
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