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Effect of Moringa Oleifera Leaves on Glycemic Control of Women With Type 2 Diabetes

Effect of Daily Consumption of Moringa Oleifera Leaves on Glycemic Control of Saharawi Women With Type 2 Diabetes

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06517602
Enrollment
52
Registered
2024-07-24
Start date
2019-11-07
Completion date
2020-02-23
Last updated
2024-07-24

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

Conditions

Type 2 Diabetes

Keywords

Moringa oleifera, Type 2 diabetes, Humans, Glucose, HbA1c

Brief summary

The objective of this clinical trial was to understand whether supplementation of Moringa oleifera leaf powder improved glycemic management in Sahrawi women with type 2 diabetes living in refugee camps. The main question sought to be answered was: \- Does daily supplementation of Moringa oleifera leaf powder, in addition to oral hypoglycemic therapy, improve glycosylated hemoglobin and fasting blood glucose? Researchers compared Moringa supplementation with no Moringa consumption to see if Moringa oleifera worked to improve glycemic control. Participants had to: * Take Moringa oleifera leaves daily or abstain from consuming Moringa for 3 months. * Consistently take prescribed oral hypoglycemic agents * Undergo clinical examinations and measurement of biochemical, metabolic and body composition parameters at the time of recruitment and at the end of the study.

Interventions

DIETARY_SUPPLEMENTSupplementation of Moringa oleifera leaf powder

Women in the experimental group were asked to consistently take the prescribed oral hypoglycemic therapy and to maintain their lifestyle and eating habits. In addition, for the duration of the study (3 months), the experimental group was provided with 10 g of Moringa oleifera leaf powder daily to be consumed with main meals.

Sponsors

University of Milan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosis of type 2 diabetes for at least 1 year * Absence of advanced retinopathy, terminal renal failure, active diabetic ulcers, amputations, and heart failure * Treatment with only oral hypoglycemic drugs.

Exclusion criteria

* Diagnosis of type 1 diabetes * Pregnancy or lactation * Treatment with insulin.

Design outcomes

Primary

MeasureTime frame
Glycosylated hemoglobin (HbA1c)Glycosylated hemoglobin was measured at recruitment and at the end of the study (three months)
Fasting glucoseFasting glucose was measured at recruitment and at the end of the study (three months)

Secondary

MeasureTime frameDescription
Hip circumferenceHip circumference were measured at recruitment and at the end of the study (3 months)
BMIBMI were measured at recruitment and at the end of the study (3 months)
Blood pressureSystolic and diastolic blood pressure were measured at recruitment and at the end of the study (3 months)Systolic and diastolic blood pressure
% body fat% of body fat were measured at recruitment and at the end of the study (3 months)
Waist circumferenceWaist circumference were measured at recruitment and at the end of the study (3 months)

Countries

Algeria

Outcome results

None listed

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