Last updated: September 28, 2023
Sponsor: University of Bath
Overall Status: Active - Recruiting
Phase
N/A
Condition
Aging
Treatment
Placebo
Ketone drink
Clinical Study ID
NCT06068803
23/SW/0067
Ages 60-80 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Age 60 to 80 years
- Postmenopausal women must be >1 year since last menses
- Able to provide informed consent
- Willing and able to comply with all study procedures including randomisation into anyof the experimental groups; maintenance of habitual dietary intake, exercise,medication and supplement use over the 28-day intervention period; blood draws andadipose tissue biopsies; and abstinence from alcohol (>24 h), food (>10 h) andstrenuous exercise (>3 d) prior to trial days.
Exclusion
Exclusion Criteria:
- Living in a residential care home
- Unstable or clinically active pulmonary, cardiac, hepatic, renal, endocrine,hematologic, immunologic, neurologic, psychiatric or biliary disorders. 'Unstable'refers to complications of a condition that are not controlled by medication orlifestyle and which require frequent monitoring and testing by a health professional.Stable chronic disease is not an exclusion criterion unless specified.
- Diagnosed Type 1 or Type 2 Diabetes Mellitus
- Diagnosed gastrointestinal condition which would potentially impact ability to consumestudy drink (e.g. inflammatory bowel disease, history of gastrointestinal ulcers orbleeding)
- Diagnosed autoimmune condition
- Previous major cardiovascular event (e.g. heart attack, stroke)
- Past or current cancer diagnosis and treatment excluding non-melanoma skin cancers
- Severe hypertension (systolic blood pressure ≥180 mmHg and/or diastolic blood pressure ≥120 mmHg), as defined by blood pressure measured at Visit 1
- Current tobacco or recreational drug use
- Reported changes to use of thyroid, antihypertensive, antidepressant or statinmedications within 30 days of Visit 1
- Taking medications that will interfere with the study outcomes
- Known negative reaction to lidocaine anaesthetic and/or taking warfarin
- Currently following a ketogenic diet or taking ketone supplements
- Not weight stable in the prior 3 months (>5% weight change)
- Unable to converse in English
Study Design
Total Participants: 30
Treatment Group(s): 2
Primary Treatment: Placebo
Phase:
Study Start date:
September 14, 2023
Estimated Completion Date:
September 30, 2025
Study Description
Connect with a study center
University of Bath
Bath, Somerset BA2 7AY
United KingdomActive - Recruiting
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