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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05737862
Other study ID # MAGPH-202210.01
Secondary ID
Status Completed
Phase Phase 3
First received
Last updated
Start date April 1, 2022
Est. completion date July 30, 2022

Study information

Verified date March 2023
Source Universitas Padjadjaran
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The main objective of this study was to compare the results of hemoglobin levels between pregnant women in the treatment group and the control group. Participants will be subjected to anthropometric measurements, recall of food intake for 1 x 24 hours, check hemoglobin before and after being given the intervention and participants in the treatment group are given moringa leaf capsules and iron tablets while participants in the control group are only given iron tablets. Researchers will compare the final results of hemoglobin levels between the treatment group and the control group


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date July 30, 2022
Est. primary completion date June 30, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 15 Years to 50 Years
Eligibility Inclusion Criteria: - Pregnant women with 2nd and 3rd trimester of pregnancy - Pregnant women with mild to moderate anemia At day 90 after treatment Exclusion Criteria : - Hypotensive pregnant women - Pregnant women with Gemelli - Pregnant women with chronic diseases (hepatitis and HIV)

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Moringa oleifera capsules
In this arm, pregnant mothers receive capsules containing 500 mg of powdered Moringa oleifera leaves which contain 13.09 mg of iron per100 gram. Dose: 2 × 2 capsules per day for 30 days
iron and folic acid supplements
In this arm, pregnant mothers receive IFA tablets 2 × 1 tablet a day for 30 days. Each IFA tablet contains 400 mcg folic acid and 180 mg Ferrous Fumarate.

Locations

Country Name City State
Indonesia University Padjajaran Bandung West Java

Sponsors (1)

Lead Sponsor Collaborator
Universitas Padjadjaran

Country where clinical trial is conducted

Indonesia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in Haemoglobin (Hb) level Hb will be meassured twice, before treatment and 30 days after treatment Day 0 and day 30
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