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NCT03456258 Clinical Trial

Lactoferrin Versus Ferrous Sulphate for the Treatment of Iron Deficiency Anemia During Pregnancy

Iron Deficiency Anemia of Pregnancy Clinical Trial

— Lactoferrin  

Official title:
Lactoferrin Versus Ferrous Sulphate for the Treatment of Iron Deficiency Anemia During Pregnancy,a Randomized Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03456258
Other study ID # Ainshams maternity hospital
Secondary ID
Status Completed
Phase N/A
First received February 23, 2018
Last updated February 28, 2018
Start date September 5, 2017
Est. completion date January 15, 2018

Study information
Verified date February 2018
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study aims to compare the efficacy and the safety of Lactoferrin versus ferrous sulphate for the treatment of iron deficiency anemia during pregnancy.

Description:

The study was done at ainshams university maternity hospital on 100 pregnant women randomized in two groups .

Group one lactoferrin group Group two ferrous sulphate group

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date January 15, 2018
Est. primary completion date December 10, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria:

- pregnant women from 20 to 40 years

- iron deficiency anemia (mild and moderate)

- gestational age 13 to 26 weeks

- singleton viable pregnancy.

Exclusion Criteria:

- history of anemia due to chronic blood loss

- hemolytic anemia

- severe anemia

- history of peptic ulcer

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• Complete blood count
To measure hemoglobin difference and serum ferritin levels .

Locations
Country Name City State
Egypt Ainshams maternity hospital Cairo Abbasia

Sponsors (1)
Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary hemoglobin level Measure hemoglobin level two months after treatment 2 months
Secondary Serum ferritin Measure serum ferritin level 2 months
See also
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Available NCT05151679 - Chelated Oral Iron Versus Intravenous Iron Sucrose for Treatment of Iron Deficiency Anemia Late in Pregnancy