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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04695418
Other study ID # 1402/22052019
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 28, 2018
Est. completion date December 27, 2019

Study information

Verified date January 2021
Source Azienda di Servizi alla Persona di Pavia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Rice germ (RG) may be a safe and effective dietary supplement for obesity in menopause, considering its high protein content and considerable amounts of essential amino acids, good fatty acids, and fiber. This pilot randomized, blinded, parallel group, placebo-controlled pilot trial investigated the effectiveness of four weeks of RG supplementation (25 g twice a day) on body composition, measured by Dual Energy X-Ray Absorptiometry (DXA), as primary outcome, and metabolic parameters, amino acid profiles and satiating capacity, as secondary outcomes, in obese postmenopausal women following a tailored hypocaloric diet (25-30% less than daily energy requirements). Twenty-seven women were randomly assigned to the supplemented group (14) or placebo group (13). There was a significant interaction between time and group for body mass index (BMI) (p<0.0001), waist (p=0.002), and hip circumference (p=0.01), total protein (0.008), albumin (0.005), Homeostasis Model Assessment index (p=0.04), glycine (p=0.002), glutamine (p=0.004), and histidine (p=0.007). Haber's means over time showed a clearly greater feeling of satiety for the supplemented compared to the placebo group. These findings indicate that RG supplementation in addition to a tailored diet counterbalanced the metabolic changes typical of menopause, with improvements in BMI, body composition, insulin resistance, amino acid profiles and satiety.


Recruitment information / eligibility

Status Completed
Enrollment 27
Est. completion date December 27, 2019
Est. primary completion date December 2, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 50 Years to 65 Years
Eligibility Inclusion Criteria: - obesity (BMI 30-40 kg/m2) - age 50-65 - menopause - sedentary women and non-smoking, - women who did not drink more than six glasses (one glass: 125 mL) of wine a week and did not drink hard liquor (alcohol content at least 20% alcohol by volume) - women who agreed not to take part in any other weight loss program Exclusion Criteria: - evidence of heart, kidney or liver disease - women who met the Diagnostic and Statistical Manual-IV (DSM-V) criteria for a current diagnosis of major depressive disorder - taking any medications for weight loss - control of cholesterol and triglycerides for anti-inflammatory purposes - pregnancy - lactating - Type 1 diabetes mellitus, irritable bowel disease, celiac disease, chronic pancreatitis - antibiotic use in the last three months - probiotic/prebiotic treatment in the last four weeks.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Rice Germ
The rice germ was taken every day (25 g in the morning with breakfast and 25 g in the afternoon as snacks) for four weeks
Combination Product:
Placebo
An isocaloric wheat germ-based supplement was taken every day (25 g in the morning with breakfast and 25 g in the afternoon as snacks) for four weeks

Locations

Country Name City State
Italy Azienda di Servizi alla Persona Pavia

Sponsors (1)

Lead Sponsor Collaborator
Azienda di Servizi alla Persona di Pavia

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of body composition free fat mass (g), fat mass (g), visceral abdominal tissue (g) Baseline and 4 weeks
Secondary Change of amino acid profiles aspartic acid, glutamic acid, alanine, arginine, asparagine, cysteine, citrulline, phenylalanine, glycine, glutamine, isoleucine, histidine, methylhistidine, methionine, ornithine, serine, tyrosine, threonine, tryptophan, valine (micromol/L) Baseline and 4 weeks
Secondary Change of biochemical metabolic parameters total serum cholesterol, triacylglycerol, HDL-cholesterol, LDL-cholesterol, apolipoprotein A, apolipoprotein B, glucose, prealbumin, iron, uric acid, creatinine, electrolytes (mg/dl) Baseline and 4 weeks
Secondary Change of biochemical metabolic parameters total proteins (g/dl) Baseline and 4 weeks
Secondary Change of biochemical metabolic parameters transaminase alanine aminotransferase, aspartate aminotransferase (IU/L) Baseline and 4 weeks
Secondary Change of biochemical metabolic parameters gamma glutamyl transferase, lipase and amylase (U/L) Baseline and 4 weeks
Secondary Change of biochemical metabolic parameters Homocysteine (micromol/L) Baseline and 4 weeks
Secondary Change of biochemical metabolic parameters Vitamin D and folic acid (ng/mL) Baseline and 4 weeks
Secondary Change of biochemical metabolic parameters Vitamin B12 (pg/ml) Baseline and 4 weeks
Secondary Change of inflammation markers C- Reactive protein (mg/dl) Baseline and 4 weeks
Secondary Change of insulin resistance Homeostasis Model Assessment (HOMA) index Baseline and 4 weeks
Secondary Change of satiating capacity Haber score (point scale) Every day for 4 weeks
Secondary Change of anthropometric measures weight (kg) Baseline and 4 weeks
Secondary Change of anthropometric measures Body mass index (Kg/m2) Baseline and 4 weeks
Secondary Change of anthropometric measures calf circumference, waist circumference, arm circumference, hip circumference (cm) Baseline and 4 weeks
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