N/A N=60 Randomized Double-blind Other

A Short-Term Appetite Suppression Trial Using Appethyl™: The Pizza

Overweight · Obesity

Bottom Line

View on ClinicalTrials.gov: NCT01919814 ↗

Enrolled (actual)

Serious AEs

1.7%

Results posted

Aug 2019

Primary outcome: Primary: Difference in Pizza Consumed During Two Meals — 1020.21; 1067.46 calories — p=>0.05

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: Appethyl™ (Dietary_supplement); Placebo (Other)
Age: Adult, Older Adult · 18+ yrs
Sex: All
Sponsor: Pennington Biomedical Research Center
Primary completion: Dec 2015

Outcome Measures

Outcome	Result	p-value
PRIMARY Difference in Pizza Consumed During Two Meals	1020.21; 1067.46	>0.05
SECONDARY Evaluation of Appetite	12.14; 15.77; 20.42; 22.13; 30.16; 37.03	—
SECONDARY Evaluation of Satiety by Means of Visual Analogue Scale	26.28; 30.53; 28.53; 34.59; 35.51; 40.62	—

Summary

The purpose of the study is to determine whether Appethyl™, made from spinach, will reduce appetite and hunger given on the same day of testing.

Eligibility Criteria

Inclusion Criteria

You are a male or female aged 18 to 65 years.
You have a BMI (a number calculated from your height and weight) between 25-35 kg/m2, inclusive.
Your waist circumference is over 35 inches.

Exclusion Criteria

You have been on a diet for weight loss in the last 2 months.
You are being treated for blood pressure, diabetes, heart disease, rheumatoid arthritis, or blood vessel disease.
You have a psychotic illness.
You have other chronic diseases like an inflammatory bowel disease such as Crohn's disease or ulcerative colitis.
You have a dysfunction of your gastrointestinal tract.
You have food allergies.
You have rheumatoid arthritis with inflammation.
You have chronic constipation.
You are taking any products to lose weight such as medication for obesity or non-prescription medications for weight loss.

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01919814). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.