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COmmencing Menopausal HOrmone Replacement Therapy and the Effect on Metabolic-dysfunction Associated Steatotic Liver Disease: a Pilot Mechanistic Study

RecruitingPhase 1Ages 18 Years - anyFemaleUniversity of Oxford
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In plain words

What the trial is, and whether it could suit you

Metabolic dysfunction-associated steatotic liver disease (MASLD) is the most common cause of chronic liver disease worldwide, currently affecting approximately 1-in-4 people globally. The prevalence is expected to rise further, driven at least partly by the epidemic of obesity and diabetes. MASLD is a condition of fat build-up in the liver that can progress to liver scarring which is associated with higher chances of death. Women are more than twice as likely to develop MASLD after menopause compared to before menopause, and previous research has shown that this may be caused by a lack of oestrogen. A lack of oestrogen is also believed to lead to harmful changes in adipose (body fat), which has an important role in the development of MASLD. Oestrogen contained in hormone replacement therapy (HRT) is an effective treatment for hot flushes and other problems in menopause. The popularity of

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: * Potential participant is willing and able to give informed consent for participation in the trial * In the Investigator's opinion, is able and willing to comply with all trial requirements * Female, aged 18 years and above * Body mass index 18 to 45 kg/m2 * Postmenopausal status: * For women โ‰ฅ 40 defined clinically (amenorrhoea for โ‰ฅ 1 year) or biochemically (FSH \>30IU/L on 2 occasions 4-6 weeks apart). * For women \< 40 defined as a combination of oligomenorrhoea/amenorrhoea for โ‰ฅ 4 months and FSH \>30IU/L on 2 occasions 4-6 weeks apart * Women who have undergone bilateral oophorectomy (no additional testing is required) * Low oestradiol levels * No exposure to systemic oestrogen-based HRT within the previous 3 months * Willing to allow his or her General Practitioner and consultant, if appropriate, to be notified of participation in the trial. Exclusion Criteria: * Potential participant with known chronic liver disease, with the exception of MASLD * The use of drugs which, in the opinion of the investigator, will significantly impact on hepatic lipid content or metabolism. This applies to drugs currently being used or used in the past, within a timeframe where the investigator believes it may impact hepatic lipid content or metabolism. * Potential participant with any other medical explanation for amenorrhoea, apart from menopause * History of harmful alcohol consumption (\>35 units/week) or alcohol misuse disorder * Potential participants with contraindication to MRI * Scheduled elective surgery or other procedures requiring general anaesthesia during the trial. * Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the trial, or may influence the result of the trial, or the participant's ability to participate in the trial. * Potential participant with life expectancy of less than 6 months. * Potential participants who have participated in another research trial involving an investigational product in the past 12 weeks. * Potential participants without a sufficient understanding of written or verbal English to participate in the study.
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What it tests

  • Menopausal hormone therapy
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Where

1 site
Oxford Centre for Diabetes Endocrinology and Metabolism (OCDEM), Churchill Hospital
Oxford, United Kingdom
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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