Colla Corii Asini Treating Anemia in Pregnant Women With Thalassemia(Presenting the Syndrome of Blood Deficiency)

Sponsor
The First Affiliated Hospital, Guangzhou University of Traditional Chinese Medicine (Other)
Overall Status
Unknown status
CT.gov ID
NCT03374111
Collaborator
(none)
480
12
2
22
40
1.8

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Drug: Colla corii asini
  • Drug: a Simulate Agent of Colla corii asini granule
Phase 4

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
480 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Parallel AssignmentParallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Masking Description:
double blind
Primary Purpose:
Treatment
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)
Actual Study Start Date :
Mar 1, 2018
Anticipated Primary Completion Date :
Oct 1, 2019
Anticipated Study Completion Date :
Dec 30, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental group

15g of Colla corii asini granule( produced by Dong-E E-Jiao Co., Ltd) , taken once daily for 8 weeks

Drug: Colla corii asini
15 g Colla corii asini granule daily for 8 weeks
Other Names:
  • donkey-hide gelatin
  • Placebo Comparator: Control group

    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

    Drug: a Simulate Agent of Colla corii asini granule
    15 g a Simulate Agent of Colla corii asini granule daily for 8 weeks
    Other Names:
  • Placebo of Colla corii asini granule
  • Outcome Measures

    Primary Outcome Measures

    1. Hemoglobin(Hb) [baseline, week 4 and week 8]

      the change of hemoglobin(g/L)

    Secondary Outcome Measures

    1. reticulocyte (RET) [baseline, week 4 and week 8]

      the change of reticulocyte (RET)count(×10^9/L)

    2. immature reticulocyte fraction(IRF) [baseline, week 4 and week 8]

      the change of immature reticulocyte fraction(%)

    3. adverse event [tracked for 42 days after giving birth]

      undesirable pregnancy outcomes

    4. indirect bilirubin(IBIL) [baseline, week 4 and week 8]

      the change of indirect bilirubin(IBIL)(μmol/L)

    5. total bilirubin(TBIL) [baseline, week 4 and week 8]

      the change of total bilirubin(TBIL) (μmol/L)

    6. lactic dehydrogenase(LDH) [baseline, week 4 and week 8]

      the change of lactic dehydrogenase(LDH)(U/L)

    7. anaemia cure rates [week 8]

      anaemia cure rates(%):The concentration of hemoglobin was higher than baseline > 5g/L;The improvement rate = improved cases/the total number of cases * 100%

    8. The curative effect of TCM Syndrome [week 8]

      the change of the TCM syndrome scores of two groups before and after treatment(%)

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 50 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    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.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 The third people's Hospital of Dongguan Dongguan Guangdong China 523326
    2 Intranet of Guangzhou Women and Children's Medical Center Guangzhou Guangdong China 510405
    3 the first affiliated hospital of Guangzhou University of Chinese Medicine Guangzhou Guangdong China 510405
    4 Department of Gynaecology and Obstetrics,Nanfang Hospital, Southern Medical University Guangzhou Guangdong China 510515
    5 The First Affiliated Hospital of Jinan University Guangzhou Guangdong China 510630
    6 The Fifth Affiliated Hospital of Guangzhou Medical University Guangzhou Guangdong China 510700
    7 Dongguan Guangji Hospital Guangzhou Guangdong China 523382
    8 Shenzhen maternity and child health care hospital Shenzhen Guangdong China 518033
    9 Liuzhou Municipal Matemal and Child Health Hospital Liuzhou Guangxi China 545001
    10 The Guangxi Zhuang Autonomous Region National Hospital Nanning Guangxi China 530001
    11 Ruikang Hospital of Guangxi University of Traditional Chinese Medicine Nanning Guangxi China 530011
    12 The First Affiliated Hospital of Guangxi University of Chinese Medicine Nanning Guangxi China 530023

    Sponsors and Collaborators

    • The First Affiliated Hospital, Guangzhou University of Traditional Chinese Medicine

    Investigators

    • Principal Investigator: Yanfang Li, PhD, the first affiliated hospital of Guangzhou University of Chinese Medicine , Guangzhou

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Yanfang Li, Director, The First Affiliated Hospital, Guangzhou University of Traditional Chinese Medicine
    ClinicalTrials.gov Identifier:
    NCT03374111
    Other Study ID Numbers:
    • TH-2
    First Posted:
    Dec 15, 2017
    Last Update Posted:
    Dec 27, 2018
    Last Verified:
    Dec 1, 2018
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Yanfang Li, Director, The First Affiliated Hospital, Guangzhou University of Traditional Chinese Medicine
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 27, 2018