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NCT Number: NCT03213639

Esomeprazole in Treatment of Early Onset Preeclampsia (ESOPE Trial)

Pre-eclampsia is one of the most serious complications of pregnancy affecting 3-8 % of pregnancies worldwide. It is a multi-system disorder involving maternal vessels (causing hypertension and endothelial dysfunction), the kidneys, the liver, the lungs, the hematological system, the cardiovascular system and the feto-placental unit. In its most severe form, it affects the brain, causing seizures (eclampsia), cerebro-vascular events and even death.

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Key information

Age range

18 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Assiut Faculty of Medicine

Asyut, Egypt

About this study

The key aspects in the pathophysiology of pre-eclampsia are placental oxidative stress (and hypoxia), placental release of the anti-angiogenic factors Soluble Fms Like Tyrosine Kinase -1 and soluble endoglin and maternal endothelial dysfunction. A drug that can counter these pathological steps could be a strategy to treat pre-eclampsia.

If an affordable and safe treatment was available it could temporize the disease progression of pre-eclampsia thereby delaying delivery to gain gestation. This could save the lives of many infants and decrease the hospital burden caused by iatrogenic prematurity.

Currently, there are trials investigating the possible use of pravastatin to treat pre-eclampsia, and to prevent it There are no other significant trials of orally available small molecules to treat pre-eclampsia that we are aware of.

The Translational Obstetrics Group at Melbourne University has generated strong preclinical evidence suggesting esomeprazole as one of the proton pump inhibitors may have potent actions giving it significant potential as a treatment for pre-eclampsia

Proton pump inhibitors have been commonly used in pregnancy to treat gastroesophageal reflux disorders and more serious gastrointestinal complications like Helicobacter pylori-infection, peptic and duodenal ulcers and Zollinger-Ellison syndrome.

Esomeprazole counters three key steps in pre-eclampsia pathogenesis, by up-regulating heme oxygenase-1 ( strongly decreasing the release of antiangiogenic factors Soluble Fms Like Tyrosine Kinase -1 and soluble endoglin and quenching endothelial dysfunction.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Gestational age between 28 + 0 weeks and 31 + 6 weeks
  • Estimated fetal weight by ultrasound between 500 gm and 1800 gm (if gestation is not certain).
  • Singleton pregnancy.
  • The patient will be managed with expectant management.

Exclusion criteria

  • Patient is unable or unwilling to give consent
  • Established fetal compromise that necessitates delivery.
  • The presence of any of the following at presentation:
  • Eclampsia.
  • Severe hypertension.
  • Cerebrovascular event as an ischaemic or haemorrhagic stroke.
  • Renal impairment.
  • Signs of left ventricular failure which include pulmonary oedema.
  • Disseminated intravascular coagulation (DIC)
  • Haemolysis, elevated liver enzymes and low platelets (HELLP syndrome)
  • Fetal distress on cardiotocography
  • Contra-indications for expectant management of pre-eclampsia
  • Current use of a proton pump inhibitor
  • Contraindications to the use of a proton pump inhibitor
  • Previous hypersensitivity reaction to a proton pump inhibitor

Treatment and study plan

Esomeprazole 40 mg Oral Tablet

Drug

once daily oral tablets

Other names: Nexium

Placebo oral tablet

Drug

once daily oral tablets

Other names: inert

Primary outcomes

  1. Number of women who develop HELLP syndrome

    Time frame: 1 month

  2. The change in serum level of sFlt-1 and endoglin before the start of treatment and at termination of pregnancy

    Time frame: 2 weeks

Secondary outcomes

  1. Prolongation of gestation measured from the time of enrollment to the time of delivery

    Time frame: 2 weeks

  2. The side effects of the drugs

    Time frame: 2 weeks

Sponsors and collaborators

Lead sponsor

Assiut University

Other

Registry information

Official study title

Use of Esomeprazole in Treatment of Early Onset Preeclampsia:a Double Blind Randomized, Placebo-controlled Trial

Important dates

Study start
2018
Primary completion
2020
Study completion
2020
First posted
Jul 11, 2017
Registry last updated
Jan 7, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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