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

Primary Purpose

Iron Deficiency Anemia of Pregnancy

Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Complete blood count
Sponsored by
Ain Shams University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Iron Deficiency Anemia of Pregnancy

Eligibility Criteria

20 Years - 40 Years (Adult)FemaleAccepts Healthy Volunteers

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

Sites / Locations

  • Ainshams maternity hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Lactoferrin

Ferrous sulphate

Arm Description

To measure hemoglobin difference and serum ferritin

To measure hemoglobin difference and serum ferritin

Outcomes

Primary Outcome Measures

hemoglobin level
Measure hemoglobin level two months after treatment

Secondary Outcome Measures

Serum ferritin
Measure serum ferritin level

Full Information

First Posted
February 23, 2018
Last Updated
February 28, 2018
Sponsor
Ain Shams University
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1. Study Identification

Unique Protocol Identification Number
NCT03456258
Brief Title
Lactoferrin Versus Ferrous Sulphate for the Treatment of Iron Deficiency Anemia During Pregnancy
Acronym
Lactoferrin
Official Title
Lactoferrin Versus Ferrous Sulphate for the Treatment of Iron Deficiency Anemia During Pregnancy,a Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2018
Overall Recruitment Status
Completed
Study Start Date
September 5, 2017 (Actual)
Primary Completion Date
December 10, 2017 (Actual)
Study Completion Date
January 15, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ain Shams University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No

5. Study Description

Brief 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.
Detailed 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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Iron Deficiency Anemia of Pregnancy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Lactoferrin
Arm Type
Experimental
Arm Description
To measure hemoglobin difference and serum ferritin
Arm Title
Ferrous sulphate
Arm Type
Experimental
Arm Description
To measure hemoglobin difference and serum ferritin
Intervention Type
Diagnostic Test
Intervention Name(s)
Complete blood count
Other Intervention Name(s)
Serum ferritin
Intervention Description
To measure hemoglobin difference and serum ferritin levels .
Primary Outcome Measure Information:
Title
hemoglobin level
Description
Measure hemoglobin level two months after treatment
Time Frame
2 months
Secondary Outcome Measure Information:
Title
Serum ferritin
Description
Measure serum ferritin level
Time Frame
2 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ahmed M Ragab, MBBCH
Organizational Affiliation
Ainshams university maternity hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ainshams maternity hospital
City
Cairo
State/Province
Abbasia
ZIP/Postal Code
11591
Country
Egypt

12. IPD Sharing Statement

Learn more about this trial

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

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