Clinical trial

Analysis of the Effect of Different Doses, Frequencies and Ways of Iron Supplements on Iron Deficiency Anemia in Pregnancy: a Randomized , Single Centered,Controlled, Single-blind Trial

Name
YXL-KY-2023(006)
Description
Subjects were tested for hemoglobin, ferritin, serum iron, transferrin saturation and reticulocyte count during routine prenatal examination at 24-26 weeks of gestation, and blood samples were taken for serum hepcidin detection in the laboratory and the values were recorded. Those who met the criteria were included in the study group, signed the informed consent form and randomized into groups, and were given different drug administration schemes (150mg orally every day, 300mg orally every day, 150mg orally every other day, 300mg orally every other day, intravenous). At the same time, each subject was given anemia diet education, and all subjects were given folic acid 400ug/d and vitamin C 0.5g/d orally during the treatment period. If the subjects were in the oral iron group, the same time of oral iron was determined as 20 o'clock ± 1 hour in the evening, and the oral iron was not taken with other drugs; If the subject is in the intravenous medication group, the medication is scheduled to be administered at a uniform time of 8 o'clock ± 1 hour in the morning. The above subjects were followed up. Hemoglobin, ferritin, serum iron, transferrin saturation and reticulocyte count were performed at 30-32 and 37 weeks of pregnancy and delivery, and blood samples were taken for serum hepcidin detection in the laboratory and the values were recorded. The adverse reactions were investigated with a questionnaire at the last prenatal examination before delivery. After full term delivery, the patient fills in the delivery information and enters it into the database. Finally, the data statistician and the above personnel used the blind method for statistical analysis and reached a conclusion.
Trial arms
Trial start
2023-03-28
Estimated PCD
2024-01-01
Trial end
2025-01-01
Status
Recruiting
Phase
Early phase I
Treatment
Niferex
Daily iron supplement scheme (QD):Oral polysaccharide iron complex capsule (Niferex)150mg/300mg daily. Alternative iron supplement scheme(QOD):Oral polysaccharide iron complex capsule(Niferex) 150mg/300mg every other day. Intravenous iron supplement(MonoFer):use as instructions
Arms:
150mg QD, 150mg QOD, 300mg QD, 300mg QOD, Intravenous iron supplement
Other names:
MonoFer
Size
452
Primary endpoint
Ferritin
37-41 weeks gestation
Elevated hemoglobin value
37-41 weeks gestation
Eligibility criteria
Inclusion Criteria: * The patient was examined and delivered at the First Affiliated Hospital of Shandong First Medical University (Qianfo Mountain Hospital of Shandong Province) * Clinical diagnosis of ID(iron depletion) * Clinical diagnosis of IDA(iron depletion anemia) * In the second trimester of pregnancy (24-26 weeks of pregnancy) * Must be able to swallow tablets * Agree to participate in the trial and sign the informed consent. Exclusion Criteria: * C-reactive protein in serum ≥5mg/L; * Clinical diagnosis of Hypertensive disorders complicating pregnancy * Clinical diagnosis of Gestational diabetes * Clinical diagnosis of Hypothyroidism * Clinical diagnosis of Chronic digestive system diseases * Clinical diagnosis of Renal insufficiency * Clinical diagnosis of psychiatric diseases * Clinical diagnosis of fetal growth restriction * Clinical diagnosis of placenta previa * Clinical diagnosis of placental abruption * Clinical diagnosis of fetal distress * Clinical diagnosis of premature rupture of membranes * Clinical diagnosis of Thalassemia * Clinical diagnosis of Hemoglobinopathy * Use anticoagulant drugs for treatment * Smoking * Excessive drinking * Clinical diagnosis of Hemorrhoids * Take acid inhibitor
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE4'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'SINGLE', 'whoMasked': ['OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 452, 'type': 'ESTIMATED'}}
Updated at
2023-04-07

1 organization

1 product

2 indications

Product
Niferex
Indication
Hemochromatosis