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Effect of Moringa Oleifera Leaf on Hemoglobin Levels in Anemia

Effect of Moringa Oleifera Leaf Capsul on Hemoglobin Levels in Anemia: A Pilot Study

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05737862
Enrollment
60
Registered
2023-02-21
Start date
2022-04-01
Completion date
2022-07-30
Last updated
2023-03-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anemia of Pregnancy

Brief 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

Interventions

DIETARY_SUPPLEMENTMoringa 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

DIETARY_SUPPLEMENTiron 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.

Sponsors

Universitas Padjadjaran
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Intervention model description

1 group receives capsules of powdered Moringa leaves (active comparator), and the other group receives IFA tablets as part of routine clinical care.

Eligibility

Sex/Gender
FEMALE
Age
15 Years to 50 Years
Healthy volunteers
Yes

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)

Design outcomes

Primary

MeasureTime frameDescription
Changes in Haemoglobin (Hb) levelDay 0 and day 30Hb will be meassured twice, before treatment and 30 days after treatment

Countries

Indonesia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026