Thalassemia Clinical Trial
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)
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.
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.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT04398628 -
ATHN Transcends: A Natural History Study of Non-Neoplastic Hematologic Disorders
|
||
Completed |
NCT04614779 -
Long-term Clinical Study of CN128 in Thalassemia Patients
|
Phase 2 | |
Completed |
NCT01158794 -
Genes Influencing Iron Overload State
|
||
Recruiting |
NCT02995707 -
The Effective and Safety of Thalidomide in NTDT
|
Phase 2 | |
Active, not recruiting |
NCT01935661 -
A Case Control Study to Evaluate the Cognitive and Brain Function of β-thalassemia Patients.
|
||
Terminated |
NCT01319851 -
Alefacept and Allogeneic Hematopoietic Stem Cell Transplantation
|
N/A | |
Completed |
NCT00901199 -
Combined Chelation Therapy in Patients With Transfusion Dependent Thalassemia and Iron Overload
|
Phase 2 | |
Terminated |
NCT00034528 -
Stem Cell Transplantation After Reduced-Dose Chemotherapy for Patients With Sickle Cell Disease or Thalassemia
|
Phase 2 | |
Active, not recruiting |
NCT03655678 -
A Safety and Efficacy Study Evaluating CTX001 in Subjects With Transfusion-Dependent β-Thalassemia
|
Phase 2/Phase 3 | |
Recruiting |
NCT05508932 -
Atrial Fibrillation in Beta-Thalassemia
|
||
Completed |
NCT03609827 -
Study of Melphalan Drug Exposure in Pediatric Hematopoietic Stem Cell Transplant Patients
|
||
Completed |
NCT03095326 -
Pneumococcal Vaccination for Splenectomised Thalassemia Major Patients in Indonesia
|
Phase 4 | |
Completed |
NCT03117192 -
Zinc Supplementation on Cellular Immunity in Thalassemia Major
|
Phase 4 | |
Completed |
NCT01443312 -
Demographic, Clinical, Laboratory and Genetical Characteristics of Patients With Beta Thalassemia Intermedia
|
||
Completed |
NCT00744692 -
Reduced Intensity Conditioning for Umbilical Cord Blood Transplant in Pediatric Patients With Non-Malignant Disorders
|
Phase 1 | |
Completed |
NCT00235391 -
Expanded Access of Deferasirox to Patients With Congenital Disorders of Red Blood Cells and Chronic Iron Overload
|
Phase 3 | |
Not yet recruiting |
NCT06058260 -
Assessment of Cognitive Function and Quality of Life in Thalassemic Children at Sohag University Hospital
|
||
Completed |
NCT05529550 -
Assessment of Nutritional Status and Role of Insulin-like Growth Factor-1 in Children
|
||
Completed |
NCT04582110 -
The Role of OCTA in Patients Affected by Beta Thalassemia
|
||
Recruiting |
NCT06213402 -
RADeep Multicenter European Epidemiological Platform for Patients Diagnosed With Rare Anemia Disorders (RADs)
|