Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
Healthy Volunteers
NCT05962190

Short-term Fat Overfeeding on the Effects of Liver Metabolism

Led by University of Oxford · Updated on 2023-07-27

26

Participants Needed

1

Research Sites

258 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Despite work showing the overconsumption of saturated fatty acids (SFA) to be metabolically deleterious, debate continues about whether there is a link between SFA and cardiovascular disease risk. To explore this, we are undertaking a human in vivo parallel-design study, comparing two isocaloric high-fat diets; one enriched with SFA and the other enriched with unsaturated fatty acids (UFAs), to determine the impact of dietary fat composition on postprandial metabolism, liver fat, cardiac fat and cardiac function.

CONDITIONS

Official Title

Short-term Fat Overfeeding on the Effects of Liver Metabolism

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Willing and able to give informed consent
  • Male or female aged 18 to 65 years
  • Body Mass Index between 19 and 35 kg/m2
  • No medical condition or medication that affects liver or fat metabolism
  • Weight stable for the past 3 months
Not Eligible

You will not qualify if you...

  • Unwilling or unable to give informed consent
  • Aged under 18 or over 65 years
  • Body Mass Index under 19 or over 35 kg/m2
  • Blood hemoglobin below 135 mg/dL for men or 120 mg/dL for women
  • Donated or lost 250 ml or more of blood in the last 2 months
  • Currently on a weight loss diet or lost more than 5% body weight in past 3 months
  • Gained more than 5% body weight in past 3 months
  • Any metabolic condition or relevant drug therapy
  • Current smoker
  • History of alcoholism or alcohol intake above recommended levels
  • Hemorrhagic disorders
  • Taking anticoagulant treatment
  • History of albumin allergy
  • Pregnant or nursing
  • Using contraceptive agents or hormone therapies in last 12 months
  • Severe claustrophobia
  • Presence of metallic implants or pacemakers
  • History of eating disorder or psychological condition affecting study adherence

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Oxford Centre for Diabetes, Endocrinology and Metabolism

Oxford, United Kingdom, OX3 7LE

Actively Recruiting

Loading map...

Research Team

L

Leanne Hodson

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here