Effect of Garlic on Gut microbiota, Inflammation & Cognition in hypertensives: The GarGIC trial
- Conditions
- hypertensionCardiovascular - HypertensionAlternative and Complementary Medicine - Herbal remediesInflammatory and Immune System - Normal development and function of the immune system
- Registration Number
- ACTRN12616000185460
- Lead Sponsor
- A/Prof Dr Karin Ried
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 50
Inclusion criteria
- Essential hypertension: Mean systolic SBP >=140 mm Hg or diastolic blood pressure >=90 mm Hg to be confirmed under trial conditions at the screening appointment (at screening mean DBP of >=88 / SBP >=135 mm Hg will be included)
- Either not on blood pressure medication, or on established plan of blood pressure medication (one or more classes) for at least 2 months
- The patient’s doctor is not planning to change current treatment during the 3 month trial
- Able to give informed consent
Exclusion criteria
- Poor comprehension of written or spoken English
- Current or previous antibiotic treatment within the last 2 months of study enrolment
- Currently taking anti-inflammatory agents, glucocorticoids or other immune regulating prescription medication
- Currently taking probiotics
- Currently taking garlic supplements
- History of intestinal surgery, inflammatory bowel disease, celiac disease, lactose intolerance, chronic pancreatitis, or diagnosed malabsorption disorder
- Planning surgery in the next 3-4 months
- Unstable other medical conditions or serious illness, at the discretion of the GP, e.g. dementia, terminal illness, recent bereavement, secondary hypertension, recent significant medical diagnosis, and pregnancy
- Severe hypertension (mean sitting SBP>=180 mm Hg and DBP >=110 mm Hg) at enrolment or subsequent visits during the study. Patients with severe hypertension will be referred back to their doctor for further management
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method