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Esomeprazole in Treatment of Early Onset Preeclampsia (ESOPE Trial)

Primary Purpose

Preeclampsia

Status
Completed
Phase
Phase 2
Locations
Egypt
Study Type
Interventional
Intervention
Esomeprazole 40 mg Oral Tablet
Placebo Oral Tablet
Sponsored by
Assiut University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Preeclampsia

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleDoes not accept healthy volunteers

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

Sites / Locations

  • Assiut Faculty of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

study group

control group

Arm Description

Patients will take esomeprazole single dose of 40 mg orally once a day

Patients will take an inert tablet similar in appearance, color and consistency

Outcomes

Primary Outcome Measures

Number of women who develop HELLP syndrome
The change in serum level of sFlt-1 and endoglin before the start of treatment and at termination of pregnancy

Secondary Outcome Measures

Prolongation of gestation measured from the time of enrollment to the time of delivery
The side effects of the drugs

Full Information

First Posted
July 8, 2017
Last Updated
January 6, 2021
Sponsor
Assiut University
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1. Study Identification

Unique Protocol Identification Number
NCT03213639
Brief Title
Esomeprazole in Treatment of Early Onset Preeclampsia (ESOPE Trial)
Official Title
Use of Esomeprazole in Treatment of Early Onset Preeclampsia:a Double Blind Randomized, Placebo-controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Completed
Study Start Date
March 15, 2018 (Actual)
Primary Completion Date
July 1, 2020 (Actual)
Study Completion Date
October 15, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Assiut University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Preeclampsia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
205 (Actual)

8. Arms, Groups, and Interventions

Arm Title
study group
Arm Type
Experimental
Arm Description
Patients will take esomeprazole single dose of 40 mg orally once a day
Arm Title
control group
Arm Type
Placebo Comparator
Arm Description
Patients will take an inert tablet similar in appearance, color and consistency
Intervention Type
Drug
Intervention Name(s)
Esomeprazole 40 mg Oral Tablet
Other Intervention Name(s)
Nexium
Intervention Description
once daily oral tablets
Intervention Type
Drug
Intervention Name(s)
Placebo Oral Tablet
Other Intervention Name(s)
inert
Intervention Description
once daily oral tablets
Primary Outcome Measure Information:
Title
Number of women who develop HELLP syndrome
Time Frame
1 month
Title
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 Outcome Measure Information:
Title
Prolongation of gestation measured from the time of enrollment to the time of delivery
Time Frame
2 weeks
Title
The side effects of the drugs
Time Frame
2 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ahmed Abbas, MD
Organizational Affiliation
Assiut University
Official's Role
Study Director
Facility Information:
Facility Name
Assiut Faculty of Medicine
City
Assiut
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
26510725
Citation
Cluver CA, Walker SP, Mol BW, Theron GB, Hall DR, Hiscock R, Hannan N, Tong S. Double blind, randomised, placebo-controlled trial to evaluate the efficacy of esomeprazole to treat early onset pre-eclampsia (PIE Trial): a study protocol. BMJ Open. 2015 Oct 28;5(10):e008211. doi: 10.1136/bmjopen-2015-008211.
Results Reference
background
PubMed Identifier
26512423
Citation
Lagana AS, Favilli A, Triolo O, Granese R, Gerli S. Early serum markers of pre-eclampsia: are we stepping forward? J Matern Fetal Neonatal Med. 2016 Sep;29(18):3019-23. doi: 10.3109/14767058.2015.1113522. Epub 2015 Nov 23.
Results Reference
background
PubMed Identifier
18771978
Citation
Baumann MU, Bersinger NA, Mohaupt MG, Raio L, Gerber S, Surbek DV. First-trimester serum levels of soluble endoglin and soluble fms-like tyrosine kinase-1 as first-trimester markers for late-onset preeclampsia. Am J Obstet Gynecol. 2008 Sep;199(3):266.e1-6. doi: 10.1016/j.ajog.2008.06.069.
Results Reference
background

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Esomeprazole in Treatment of Early Onset Preeclampsia (ESOPE Trial)

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