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Clinical Trials/CTRI/2019/08/020863
CTRI/2019/08/020863
Not 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 enrollmentTBD
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ConditionsHealth Condition 1: O098- Supervision of other high risk pregnancies

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: O098- Supervision of other high risk pregnancies
Sponsor
il
Status
Not yet recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
il

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

Outcomes

Primary Outcomes

Not specified

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