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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03654651
Other study ID # use PKE_PEANUT
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date October 1, 2018
Est. completion date December 20, 2019

Study information

Verified date August 2023
Source Penn State University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A two-period randomized crossover study will be conducted to determine the effect of peanuts on glycemic control, and elucidate the role of the microbiome in glucose regulation, in individuals with impaired fasting glucose.


Description:

A two-period randomized crossover trial will be conducted. Participants will be randomized to receive each treatment for 6 weeks followed by a minimum 4-week wash-out period. During the peanut treatment, participants will consume one ounce per day (28 g) of peanuts as an evening snack. The control treatments will be an isocaloric higher carbohydrate snack consumed after the evening meal. Markers of glycemic control, cardiovascular risk factors and gut health will be assessed at the beginning and the end of each treatment period.


Recruitment information / eligibility

Status Completed
Enrollment 51
Est. completion date December 20, 2019
Est. primary completion date December 20, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Non-smoking - Impaired fasting glucose at screening (= 100 mg/dL). - BMI =20 and =40 kg/m2. Exclusion Criteria: - Diagnosed diabetes or fasting glucose >126 mg/dl - Systolic blood pressure >160mmHg or diastolic blood pressure >100mmHg) - Prescribed anti-hypertensive, lipid lowering or glucose lowering drugs - Established cardiovascular disease, stroke, diabetes, liver, kidney or autoimmune disease or inflammatory conditions - Use of supplements (psyllium, fish oil, soy lecithin, phytoestrogens) and botanicals and not willing to cease for the duration of the study - Pregnancy or lactation - Weight loss of >=10% of body weight within the 6 months prior to enrolling in the study - Smoking or use of any tobacco products - Allergy to test foods - Consumption of >14 alcoholic drinks/week

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Peanut
Roasted, unsalted peanuts will be purchased from a local grocery store and provided to subjects to consume.
High carbohydrate snack
Whole wheat crackers will be purchased from a local grocery store and provided to subjects to consume with a spread (e.g. cream cheese or margarine).

Locations

Country Name City State
United States Pennsylvania State University University Park Pennsylvania

Sponsors (2)

Lead Sponsor Collaborator
Penn State University The Peanut Institute

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fasting Plasma Glucose Within-condition mean differences (change from baseline). 6 weeks
Secondary Fructosamine Within-condition mean differences (change from baseline). 6 weeks
Secondary Fasting Insulin Within-condition mean differences (change from baseline). 6 weeks
Secondary Peripheral Systolic and Diastolic Blood Pressure Within-condition mean differences (change from baseline). 6 weeks
Secondary Central Systolic and Diastolic Blood Pressure Within-condition mean differences (change from baseline). 6 weeks
Secondary Carotid Femoral Pulse Wave Velocity Carotid-femoral pulse wave velocity is a measure of arterial stiffness and is determined from the time taken for the arterial pulse to propagate from the carotid to the femoral artery.
Within-condition mean differences (change from baseline).
6 weeks
Secondary Augmentation Index (%) A measure of arterial stiffness assessed using a SphymoCor Ecel (Atcor Medical). A higher percentage value is indicative of greater arterial stiffness
Within-condition mean differences (change from baseline).
6 weeks
Secondary LDL Cholesterol Within-condition mean differences (change from baseline). 6 weeks
Secondary HDL Cholesterol Within-condition mean differences (change from baseline). 6 weeks
Secondary Total Cholesterol Within-condition mean differences (change from baseline). 6 weeks
Secondary Triglycerides Within-condition mean differences (change from baseline). 6 weeks
Secondary Body Weight Within-condition mean differences (change from baseline). 6 weeks
Secondary Microbiota Alpha-diversity Measured by Faith's Phylogenetic Diversity Score. This is a measure of biodiversity (based on phylogeny). Faith's phylogenetic diversity measures the amount of the phylogenetic tree covered by the bacterial community. It's a sum of the minimum branch lengths. A higher number (more branches), means more richness (more diversity). Increases in Faith's Phylogenetic Diversity is indicative of more richness and diversity but no standard reference range or clinically relevant values have been established.
Presented as endpoint mean values with IQR
6 weeks
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