Status:

UNKNOWN

Sulforaphane Supplementation Study

Lead Sponsor:

University of Oxford

Collaborating Sponsors:

Quadram Institute Bioscience

Conditions:

Non-Alcoholic Fatty Liver Disease

Obesity

Eligibility:

All Genders

18-65 years

Phase:

NA

Brief Summary

Non-alcoholic fatty liver disease (NAFLD) is increasing in the population, and is associated with heart disease and diabetes. At present there are no licensed drugs for treatment of NAFLD, therefore c...

Detailed Description

Participants satisfying the inclusion criteria will be invited to the Oxford Centre for Clinical Magnetic Resonance Research (OCMR), to measure the amount of fat within their liver and heart using mag...

Eligibility Criteria

Inclusion

  • Participant is willing and able to give informed consent for participation in the study.
  • Healthy adults, Male or Female, aged 18 to 65 years.
  • No medical condition or relevant drug therapy known to affect glucose or fatty acid metabolism.
  • Weight stable for the previous 3 months. -

Exclusion

  • Aged ≤18 or ≥65 years.
  • Body Mass Index ≤19 or ≥35kg/m2.
  • Females with a body mass ≤50kg.
  • A blood haemoglobin \<135mg/dL for men and \<120mg/dL for women.
  • Donated (or lost) ≥250 ml of blood in the previous two months.
  • On a weight loss diet or have decreased their body weight by \>5% in the previous 3 months.
  • Have increased their body weight by \>5% in the previous 3 months.
  • Any metabolic condition or relevant drug therapy known to affect glucose or fatty acid metabolism.
  • Smoking, or use of nicotine replacement agents (e.g. e-cigarettes).
  • History of alcoholism or a greater than recommended alcohol intake (\>30 g of alcohol daily for men and \>20 g of alcohol daily for women).
  • Current or history of Haemorrhagic disorders.
  • History of albumin allergy or allergic to eggs
  • Current or history of anticoagulant treatment.
  • Pregnant or nursing mothers.
  • Women prescribed any hormone replacement therapy (HRT) or who have used these within the last 12 months.
  • History of severe claustrophobia.
  • Presence of metallic implants, pacemaker, or inability/unwillingness to remove any piercings, and any large tattoos around the area to be scanned.
  • History or current psychiatric illness.
  • History or current neurological condition (e.g. epilepsy).

Key Trial Info

Start Date :

January 1 2020

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

August 1 2023

Estimated Enrollment :

60 Patients enrolled

Trial Details

Trial ID

NCT04364360

Start Date

January 1 2020

End Date

August 1 2023

Last Update

June 7 2022

Active Locations (1)

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Oxford Centre for Diabetes, Endocrinology and Metabolism

Oxford, Oxfordshire, United Kingdom, OX3 7LE