Byuderma Clinic
Bekasi, West Java, 17131, Indonesia
NCT Number: NCT07833397
The goal of this clinical trial was to learn whether Moringa oleifera leaf powder could lower fasting blood glucose in adults aged 25 to 55 years with prediabetes. It also assessed unwanted health effects during the intervention. The main questions it aimed to answer were:
* Does taking Moringa oleifera leaf powder daily for 90 days lower fasting blood glucose compared with a placebo? * What unwanted health effects occur while participants take Moringa oleifera leaf powder or placebo?
Researchers compared Moringa oleifera leaf powder with matching placebo capsules that contained no Moringa.
Participants:
* Were randomly assigned to receive Moringa oleifera leaf powder or placebo * Took six 400-mg capsules daily, as two capsules three times a day after meals, for 90 days * Measured and recorded fasting blood glucose at baseline and every 3 days during the study * Reported adherence and any unwanted health effects
Looking for future studies?
Notify Me25 year–55 year
All sexes
Interventional
Not applicable
Bekasi, West Java, 17131, Indonesia
This was a prospective, randomized, double-blind, placebo-controlled, parallel-group clinical trial conducted in a primary care setting in Bekasi, Indonesia. The study evaluated the effect of Moringa oleifera leaf powder on fasting blood glucose over 90 days in adults with prediabetes.
Eligible participants were adults aged 25 to 55 years with fasting blood glucose levels of 100-125 mg/dL who had not used oral antidiabetic medication or insulin during the preceding 3 months. After providing informed consent, 114 participants were randomly assigned in a 1:1 ratio to the Moringa oleifera leaf powder group or the placebo group.
Participants in the intervention group received 2,400 mg of Moringa oleifera leaf powder daily as six 400-mg capsules, taken as two capsules three times daily after meals for 90 days. Participants in the control group received matching microcrystalline cellulose placebo capsules according to the same schedule.
Fasting blood glucose was measured at baseline and every 3 days through day 90. The primary objective was to compare the longitudinal pattern of fasting blood glucose between the two groups. Treatment adherence and unwanted health effects were also monitored throughout the study.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Standardized Moringa oleifera leaf powder provided in 400-mg oral capsules. Participants received 2,400 mg daily as two capsules three times daily after meals for 90 days.
Time frame: Baseline and every 3 days through Day 90 (31 time points).
Fasting blood glucose was measured in milligrams per deciliter (mg/dL) using a validated capillary blood glucose monitoring device. Repeated measurements were used to evaluate the fasting blood glucose trajectory and differences between the two treatment groups over the 90-day intervention.
Maranatha Christian University
Other
Effect of Moringa Oleifera Leaf Powder on Fasting Blood Glucose Levels in Adults With Prediabetes: A Randomized, Double-Blind, Placebo-Controlled Trial
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07618663
Diabetes Mellitus, Endocrine System Diseases
Lahore, Shaikhupura, Pakistan
View Trial DetailsNCT06895161
Diabetes Mellitus, Endocrine System Diseases
Ankara, Turkey (Türkiye)
View Trial DetailsNCT06867198
Adult, Arterial Stiffness, Blood Pressure
Atlanta, Georgia, United States
View Trial DetailsNCT07553325
Diabetes Mellitus, Endocrine System Diseases
Frederick, Maryland, United States
View Trial Details