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Effects of Moringa Oleifera Leaves on Glycemia, Lipemia and Inflammatory Profile in Prediabetic Patients (NUTRIMOL-DB)

Primary Purpose

PreDiabetes

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Moringa
Placebo
Sponsored by
National Research Council, Spain
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for PreDiabetes focused on measuring Moringa oleifera, functional food, anti-hyperglycemic effect, prevention, anti-inflammatory, microbiota, lipid metabolism

Eligibility Criteria

40 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Prediabetes: HbA1c between 5.7-6.4 % or fasting blood glucose between 100 - 125 mg/dl or impaired glucose tolerance (> 140 mg/dl and < 200 mg/dl two hours post oral challenge).
  • No pharmacological treatment prescribed for glycemia control.

Exclusion Criteria:

  • Diabetes Mellitus
  • Impaired renal function: < 60% Glomerular filtration
  • Uncontrolled high blood pressure
  • Previous cardiovascular events or coronary disease
  • Autoimmune disease
  • HIV
  • Severe gastrointestinal disease
  • Cancer
  • Psychiatric illness
  • Elevated liver enzymes (x2 normal range)
  • Alcohol abuse (higher than 14 and 21 doses/week for women and men, respectively)
  • Morbid obesity (BMI>35kg/m2)
  • Pregnancy
  • Pharmacological treatments that interfere with glucose control.

Sites / Locations

  • Institute of Food Science and Technology and Nutrition (ICTAN)-CSIC

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Moringa

Placebo

Arm Description

Six Moringa oleifera capsules (400 mg dry leaf powder /capsule) consumed daily during 12 weeks. Two capsules consumed with each of the three main meals.

Six placebo capsules containing microcrystalline cellulose consumed daily during 12 weeks. Two capsules consumed with each of the three main meals.

Outcomes

Primary Outcome Measures

Fasting Blood Glucose
Measured in serum samples from fasting blood withdrawn in a Sodium Fluoride vacutainer tube
Glycated hemoglobin (HbA1C)
Measured in fasting serum

Secondary Outcome Measures

Conversion rate from prediabetes to normal
Number of subjects in each arm that convert from prediabetic to normal glycemia

Full Information

First Posted
January 27, 2021
Last Updated
February 2, 2021
Sponsor
National Research Council, Spain
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1. Study Identification

Unique Protocol Identification Number
NCT04734132
Brief Title
Effects of Moringa Oleifera Leaves on Glycemia, Lipemia and Inflammatory Profile in Prediabetic Patients
Acronym
NUTRIMOL-DB
Official Title
Effects of Moringa Oleifera Leaves on Glycemia, Lipemia and Inflammatory Profile. Nutritional Intervention Study in Prediabetic Patients
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
January 22, 2019 (Actual)
Primary Completion Date
May 5, 2020 (Actual)
Study Completion Date
January 26, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National Research Council, Spain

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Moringa oleifera (MO) is a traditional food in tropical and subtropical areas and has attained a growing interest for its medicinal properties. It's a nutrient-rich vegetable, high in protein and polyphenol content. The MO dry leaves and leaf extracts have been shown to exert numerous in vitro activities and in vivo effects, including the hypoglycemic effect. Thus, MO could be an alternative to prevent or treat diabetes. Studies in humans, however, are still limited. This proposal aims to study the efficacy of Moringa oleifera to improve the control of glycaemia in subjects with prediabetes. A 3-month dietary intervention with MO dry leave capsules will be performed and compared to placebo.
Detailed Description
The tree Moringa oleifera (MO) is a traditional medicinal plant in tropical and subtropical areas, also consumed as food, which is currently expanding worldwide as a protein-rich leafy vegetable and for the medicinal value of its phytochemicals, in particular its glucosinolates. Specifically, MO dry leaves and leaf extracts have been shown to exert numerous in vitro activities and in vivo effects, including the hypoglycemic effect. Thus, MO could be an alternative to prevent or treat diabetes. In this sense, in vitro and preclinical experiments have shown that MO could potentially reverse some of the pathophysiological manifestation of diabetes and its comorbidities, such as hepatic fat accumulation and insulin resistance, oxidative stress, inflammation and peripheral hyperglycemia. Studies in humans, however, are still limited. This proposal aims to study the efficacy of Moringa oleifera to improve the control of glycaemia in subjects with prediabetes. A 3-month dietary intervention with MO dry leave capsules will be performed and compared to placebo. This will be a double-blind, randomized, placebo controlled, parallel group intervention study. Subjects will randomly consume either 6 capsules of dry MO leaves (400 mg dry leaf powder /capsule) or 6 placebo capsules per day during 3 months. The study subjects will provide samples for outcome measurements at three different time points: basal, 6 weeks and 12 weeks of supplementation. Glycaemia and plasma inflammatory and metabolic markers will be measured, as well as the gut microbiota composition.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
PreDiabetes
Keywords
Moringa oleifera, functional food, anti-hyperglycemic effect, prevention, anti-inflammatory, microbiota, lipid metabolism

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Double blind, randomized, parallel group, placebo-controlled dietary intervention in prediabetic subjects.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
One member of the research team was in charge of product preparation and delivery to the participants following the randomization list.
Allocation
Randomized
Enrollment
72 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Moringa
Arm Type
Experimental
Arm Description
Six Moringa oleifera capsules (400 mg dry leaf powder /capsule) consumed daily during 12 weeks. Two capsules consumed with each of the three main meals.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Six placebo capsules containing microcrystalline cellulose consumed daily during 12 weeks. Two capsules consumed with each of the three main meals.
Intervention Type
Dietary Supplement
Intervention Name(s)
Moringa
Intervention Description
Leaves of Moringa oleifera from an organic Iberian peninsula cultivar. A single lot was prepared from the same crop. Leaves were dried and ground and encapsulated as a organic dietary supplement. No other changes in diet or physical activity were included although a general healthy lifestyle pattern was recommended.
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Placebo capsules were indistinguishable from the experimental capsules in material and color (opaque white). Same number of capsules were consumed as in the experimental arm and no other changes in diet or physical activity were included although a general healthy lifestyle pattern was recommended.
Primary Outcome Measure Information:
Title
Fasting Blood Glucose
Description
Measured in serum samples from fasting blood withdrawn in a Sodium Fluoride vacutainer tube
Time Frame
12 weeks
Title
Glycated hemoglobin (HbA1C)
Description
Measured in fasting serum
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Conversion rate from prediabetes to normal
Description
Number of subjects in each arm that convert from prediabetic to normal glycemia
Time Frame
12 weeks
Other Pre-specified Outcome Measures:
Title
Total serum cholesterol concentration and lipoprotein-cholesterol concentrations
Description
Serum lipid profile
Time Frame
12 weeks
Title
Concentration of inflammatory markers
Description
C-reactive protein, interleukin (IL)-1beta, IL-6, Tumour necrosis factor-alpha, Macrophage chemoattractant protein-1
Time Frame
12 weeks
Title
Concentration of metabolic hormones
Description
Insulin, Glucagon like peptide-1, Peptide YY, leptin, adiponectin, ghrelin,
Time Frame
12 weeks
Title
Antioxidant capacity
Description
Total antioxidant capacity of the lipid soluble fraction of plasma by chemiluminescent method (Photochem)
Time Frame
12 weeks
Title
Microbiota composition
Description
Quantitative analysis of main representative bacteria groups of gut microbiota by quantitative polymerase chain reaction
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Prediabetes: HbA1c between 5.7-6.4 % or fasting blood glucose between 100 - 125 mg/dl or impaired glucose tolerance (> 140 mg/dl and < 200 mg/dl two hours post oral challenge). No pharmacological treatment prescribed for glycemia control. Exclusion Criteria: Diabetes Mellitus Impaired renal function: < 60% Glomerular filtration Uncontrolled high blood pressure Previous cardiovascular events or coronary disease Autoimmune disease HIV Severe gastrointestinal disease Cancer Psychiatric illness Elevated liver enzymes (x2 normal range) Alcohol abuse (higher than 14 and 21 doses/week for women and men, respectively) Morbid obesity (BMI>35kg/m2) Pregnancy Pharmacological treatments that interfere with glucose control.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Esther NOVA, PhD
Organizational Affiliation
National Research Council of Spain
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institute of Food Science and Technology and Nutrition (ICTAN)-CSIC
City
Madrid
ZIP/Postal Code
28040
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
Although a specific plan has not been conceived yet, sharing research data is a good practice that the investigators would pursue at due time.
Citations:
PubMed Identifier
32664295
Citation
Nova E, Redondo-Useros N, Martinez-Garcia RM, Gomez-Martinez S, Diaz-Prieto LE, Marcos A. Potential of Moringa oleifera to Improve Glucose Control for the Prevention of Diabetes and Related Metabolic Alterations: A Systematic Review of Animal and Human Studies. Nutrients. 2020 Jul 10;12(7):2050. doi: 10.3390/nu12072050.
Results Reference
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PubMed Identifier
31810205
Citation
Vargas-Sanchez K, Garay-Jaramillo E, Gonzalez-Reyes RE. Effects of Moringa oleifera on Glycaemia and Insulin Levels: A Review of Animal and Human Studies. Nutrients. 2019 Dec 2;11(12):2907. doi: 10.3390/nu11122907.
Results Reference
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Effects of Moringa Oleifera Leaves on Glycemia, Lipemia and Inflammatory Profile in Prediabetic Patients

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