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Clinical Trials/CTRI/2019/08/020863
CTRI/2019/08/020863Not yet recruiting未知

A randomized controlled trial comparing the efficacy, tolerability and cost of oral iron preparations in iron deficiency anemia in pregnancy

il0 sites0 target enrollmentStarted: TBDLast updated:
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Trial Snapshot

Phase
未知
Status
Not yet recruiting
Sponsor
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Inclusion Criteria

  • •1.Pregnant women with age between 20 and 40 years and period of gestation from 12 to 30 weeks.
  • •2.Hemoglobin ranging from 7 to 10.5 g% at the start of the study
  • •3.Treatment naïve patients
  • •4.Singleton pregnancy
  • •5.Patients willing to give written informed consent

Exclusion Criteria

  • •1.Pregnant women with any other types of anemia such as megaloblastic anemia, thalassemia, sickle cell anemia, anemia of chronic disease, hemolytic anemia and anemia due to chronic blood loss.
  • •2.Pregnant women with Hb <7 g% & Hb >10.5g%
  • •3.Pregnant women with known hypersensitivity to iron preparations
  • •4.Pregnant women with any other comorbidities such as renal or hepatic impairment, cardiovascular diseases, preeclampsia, GDM, thyroid disorders, acid peptic disease, esophagitis and malabsorption syndrome.
  • •5.Treatment with any other investigational drug in the last 1 month before study entry
  • •6.Multiple pregnancy

Investigators

Sponsor
il

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