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Effects of intestinal Amarasate™ (a bitter hops extract) on gut function in healthy, lean volunteers.

Not Applicable
Completed
Conditions
Type 2 Diabetes
Healthy human gastrointestinal physiology
Obesity
Diet and Nutrition - Obesity
Oral and Gastrointestinal - Normal oral and gastrointestinal development and function
Metabolic and Endocrine - Diabetes
Registration Number
ACTRN12620000503921
Lead Sponsor
Professor Christine Feinle-Bisset
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Male
Target Recruitment
11
Inclusion Criteria

A total of 12 healthy, lean (BMI 19-25 kg/m2) male subjects, aged between 18 - 60 years will be included. Subjects will be required to be weight stable (ie <5% fluctuation) at study entry, which will be ascertained by a stable body weight in the preceding 4 weeks.

Exclusion Criteria

Significant GI symptoms, disease or surgery
Use of prescribed or non-prescribed medications (including vitamins and herbal Supplements) which may affect energy metabolism, GI function, body weight or appetite (eg domperidone, cisapride, anticholinergic drugs (eg atropine), metoclopramide, erythromycin, hyoscine, orlistat, green tea extracts, Astragalus, St Johns Wort etc.)
Lactose intolerance/other food allergy(ies), including hops allergy, diagnosed idiopathic anaphylaxis or occupational exposure to hops (hops pickers, brewers)
Current gallbladder or pancreatic disease
Cardiovascular or respiratory diseases
Individuals with low ferritin levels (<30 ng/mL), or who have donated blood in the 12 weeks prior to taking part in the study
Any other illnesses as assessed by the investigator (including chronic illnesses not explicitly listed above)
High performance athletes
Current intake of > 2 standard drinks on > 5 days per week
Current smokers of cigarettes/cigars/marijuana
Recreational drug use
Current intake of any illicit substance
Vegetarians
Inability to tolerate nasogastric tube
Inability to comprehend study protocol
Restrained eaters (score >12 on the 3-factor eating questionnaire)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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