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Active RESEARCH NIHR Open Data-Funded Portfolio

A multi-centre, double-blind, placebo-controlled randomised trial comparing a combination of methotrexate and mifepristone versus methotrexate alone as a medical treatment for tubal ectopic pregnancy (Short title - AMETHYST Trial: Adding Mifepristone to mETHotrexate for ectopic pregnancY STudy)

£169.76M GBP

Funder National Institute for Health and Care Research
Recipient Organization University of Aberdeen
Country United Kingdom
Start Date Nov 01, 2024
End Date Jul 31, 2028
Duration 1,368 days
Number of Grantees 2
Roles Principal Investigator; Award Holder
Data Source NIHR Open Data-Funded Portfolio
Grant ID NIHR160933
Grant Description

BACKGROUND Ectopic pregnancy (EP) affects 1 in 90 pregnancies and is the leading cause of death in the first trimester of pregnancy. An EP is a pregnancy implanted in an abnormal location, usually within the Fallopian tube (tubal EP; tEP). As the EP grows, the Fallopian tube is at risk of rupture which can cause life-threatening internal bleeding.

Historically, the only treatment was surgery to remove the affected Fallopian tube. More recently, advances in ultrasound and biochemical markers of pregnancy have enabled diagnosis at an earlier stage so medical or expectant management can be offered. NICE(NG126) endorses medical treatment with methotrexate (MTX), an antifolate drug.

Although 40% of women with tEP are now treated medically, 15% need a second injection of MTX and 30% will require surgery to remove the EP. We propose that an antiprogesterone drug, mifepristone, could improve the efficacy of MTX treatment compared to MTX alone. Mifepristone is routinely used in the management of miscarriage and termination of pregnancy. Evidence suggests there could be a role for mifepristone in tEP but a definitive trial is needed.

AIM To determine if the combination of mifepristone and MTX is more effective than MTX alone with placebo in reducing the need for surgical intervention in clinically stable women with tEP. We will explore how mifepristone affects the trajectory of key pregnancy hormones (progesterone and hCG) and whether any treatment effect is moderated and/or mediated by the woman’s own baseline levels of pregnancy hormones.

METHODS - DESIGN: Multicentre, double blind, placebo-controlled randomised controlled trial POPULATION: Clinically stable women aged 16-years and over with tEP and hCG level of 1000-5000 IU/L who have opted for standard medical treatment with single dose intramuscular methotrexate (50mg/m2) INTERVENTION: 600mg mifepristone (3 tablets taken once) COMPARATOR Matched placebo (3 tablets taken once) ASSESSMENT: Assessments will follow a protocol mirroring usual clinical care. Assessment of clinical suitability and hCG and progesterone levels in maternal serum at baseline, on days 1,4,7,11 and then weekly until hCG

All Grantees

University of Aberdeen

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