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Preeclampsia SeverePhase 4NCT06359015

Metformin and Esomeprazole in Preterm Pre-eclampsia

A Phase 4 study testing Metformin and Esomeprazole in people with Preeclampsia Severe and Pre-Eclampsia, run by Christiana Care Health Services at 1 site in United States.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

The purpose of this study is to better understand diagnosis and treatment of preterm preeclampsia. Currently, there are limited laboratory tests that can be used to diagnosis preeclampsia. Additionally, there are few treatments for this condition. Read more about this study

Who is it for?
Ages 18 to 60 years, women only
Conditions the study is for
Preeclampsia Severe, Pre-Eclampsia, Preeclampsia
What is being tested?
Metformin and Esomeprazole
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
4 participants
Where
1 siteUnited States
Study dates
11 Feb 2021to 8 May 2025
Phase
Phase 4
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 60 years
  • Women only
  • No healthy volunteers
  • Adult

Who may be able to join

  • Women 18 years or older
  • Women diagnosed with preeclampsia or preeclampsia with severe features or superimposed preeclampsia with chronic hypertension
  • Candidates for expectant management and had no clinical indication for immediate delivery

Who cannot join

  • Delivery within 48hr is highly likely
  • Maternal or fetal compromise that necessitated immediate delivery
  • Diabetes or gestational diabetes currently on metformin therapy
  • Reflux disease or other conditions currently on esomeprazole
  • Contraindications to metformin, esomeprazole
  • Baseline creatinine >124 μmol/L
Show all 11Show fewer
  • Hypersensitivity to metformin or esomeprazole
  • Current use of metformin or esomeprazole
  • Metabolic acidosis
  • Use of drugs that might interact with metformin (glyburide, furosemide, or cationic drugs)
  • Multiple gestations

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Christianacare Health System

    Newark, Delaware, 19718

Other trials in United States

About this study

Official title: Use of Combination Metformin and Esomeprazole in Preterm Pre-eclampsia: a Randomized Controlled Trial

The purpose of this study is to better understand diagnosis and treatment of preterm preeclampsia. Currently, there are limited laboratory tests that can be used to diagnosis preeclampsia. Additionally, there are few treatments for this condition. This clinical trial will explore treatment options, Metformin and Esomeprazole, as well as serum markers that could improve the diagnosis and treatment of preterm preeclampsia.

Read the detailed description

BACKGROUND:

The pathophysiology of preeclampsia

To achieve normal vascular function during pregnancy, the placental vascular endothelium secretes vasoactive substances and growth factors, most notably vascular endothelial growth factor (VEGF), sFlt-1, placental growth factor (PlGF) and soluble endoglin (sEng). These substrates interact with maternal natural killer cells to promote remodeling of the uterine spiral arteries in order to create a uteroplacental interface. Circulating vasoconstrictors, such as Thromboxane A2, and vasodilators play an important role in regulating the vascular endothelium in response to the developing uteroplacental interface.

In patients with preeclampsia, however, trophoblast cells demonstrate insufficient invasion of the spiral arteries, leading to poor remodeling, narrow vessel diameter and high vascular resistance. The endothelial dysfunction occurs in two phases. In the first phase, defective placental trophoblastic invasion of the uterine spiral arteries occurs at 14-18 weeks of gestation. This dysfunctional invasion leads to poor uteroplacental blood flow and the release of antiangiogenic factors and vasoconstrictive substances in the second phase.

In Defense of Metformin, Esomeprazole

Lower sFlt1 levels were detected in placental villous explants from patients diagnosed with preterm preeclampsia and treated with metformin. Metformin downgraded endothelial cell secretion by 53% and placental cell secretion by 63%. Similarly, in a meta-analysis of patients on metformin for gestational diabetes (GDM), Kalafat and Sukur concluded that the use of metformin was associated with a reduced risk of preeclampsia (relative risk (RR): 0.56; 95% confidence interval (CI): 0.37-0.85; n = 1260 women)

A recent randomized controlled trial by Cluver et al included 180 women with preterm pre-eclampsia between 26+0 to 31+6 weeks' gestation undergoing expectant management: 90 were randomized to extended release metformin and 90 to placebo. Investigators found that extended release metformin (3g daily) can prolong gestation in women with preterm pre-eclampsia

In vitro studies show proton pump inhibitors decrease soluble fems like tyrosine kinase -1 (sFlt-1) and soluble endoglin and improve markers of endothelial dysfunction. Esomeprazole reduces blood pressure in a preeclampsia transgenic mouse model that overexpresses sFlt-1.

Combination metformin and esomeprazole has shown promise in the treatment of preeclampsia as both agents reduce placental and endothelial secretion of sFlt-1 and soluble endoglin, and reduce endothelial dysfunction. Kaitu'u-Lino et al found that combining metformin and esomeprazole was additive at reducing sFlt-1 secretion and expression of sFlt-1 e15a mRNA isoform in primary cytotrophoblast, placental explants and endothelial cells.

Safety of Metformin, Esomeprazole

Metformin is a biguanide that inhibits hepatic gluconeogenesis and glucose absorption and stimulates glucose uptake in peripheral tissues.

In one large trial, 751 women with GDM were randomly assigned to receive insulin therapy or metformin. Both groups experienced similar rates of a composite outcome of perinatal morbidity, consisting of neonatal hypoglycemia, respiratory distress, need for phototherapy, birth trauma, prematurity, and low Apgar scores. Additionally, five randomized clinical trials showed the safety of metformin as well as its efficiency in dealing with GDM compared with insulin. A meta-analysis by Gui et al. demonstrated that metformin was superior to insulin in reducing the incidence of preeclampsia.

Proton pump inhibitors (PPI) such as esomeprazole have long-term safety data in the treatment of gastric reflux in pregnancy. The Motherisk Program conducted a meta-analysis on use of PPIs in 593 pregnancies and showed no increase in risk of malformations. Furthermore, in a large cohort study from the Swedish Medical Birth Registry on 955 infants whose mothers used PPIs during pregnancy showed no difference in birth weights, rates of congenital malformations, perinatal death, or low Apgar scores.

Being tested
Metformin, Esomeprazole
Keywords
Metformin, Esomeprazole, Preterm Preeclampsia, Preeclampsia with Severe Features, Superimposed Preeclampsia with Severe Features
Medical subject headings
Pre-Eclampsia, Premature Birth

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • MetforminDrug

    Oral Metformin schedule:

    Day 1: 500 milligrams in morning Day 2: 500 milligrams two times a day Day 3: 1000 milligrams in morning, 500 milligrams in evening Day 4 onwards: 1000 milligrams two times a day based on individual tolerance

    Oral Esomeprazole schedule:

    40 milligrams Oral Esomeprazole daily until delivery which can be tapered down to 20 milligrams daily based on individual tolerance.

  • EsomeprazoleDrug

    40 milligrams Oral Esomeprazole daily until delivery which can be tapered down to 20 milligrams daily based on individual tolerance.

Study groups in NCT06359015
Study groupRoleWhat they receive
Metformin and EsomeprazoleExperimentalPatients diagnosed with preterm preeclampsia receive expectant management with additional metformin/esomeprazole.
Receives: Drug: Metformin; Drug: Esomeprazole
No InterventionNo interventionPatients diagnosed with preterm preeclampsia receive expectant management only.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Mean plasma difference in sFlt-1

    sFlt-1 from serum samples

    Measured: Over the first 14 days after randomization and during the remainder of pregnancy, an average of 3-4 months

Secondary outcomes (5)
  1. Mean plasma difference in vascular endothelial growth factor (VEGF)

    VEGF from serum samples

    Measured: Over the first 14 days after randomization and during the remainder of pregnancy, an average of 3-4 months

  2. Mean plasma difference in placental growth factor (PIGF)

    PIGF from serum samples

    Measured: Over the first 14 days after randomization and during the remainder of pregnancy, an average of 3-4 months

  3. Mean plasma difference in soluble endoglin (sEng)

    sENG from serum samples

    Measured: Over the first 14 days after randomization and during the remainder of pregnancy, an average of 3-4 months

  4. sFlt-1:PIGF ratio

    sFLT-1:PIGF from serum samples

    Measured: Over the first 14 days after randomization and during the remainder of pregnancy, an average of 3-4 months

  5. Prolongation of gestation

    Difference in time of expectant management between experimental and control group.

    Measured: Over the first 14 days after randomization and during the remainder of pregnancy, an average of 3-4 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Apr 2024
  2. Study start11 Feb 2021
  3. Primary completion8 May 2025
  4. Study completion8 May 2025

Why it stopped: Lost funding

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
There are two groups: experimental and control. The control group receives expectant management. The experimental group receives expectant management and medication treatment.
Masking
None (open label)
Enrolment
4 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06359015
Sponsor's protocol ID
41138
Other IDs
605095
Status last verified
May 2025
First submitted
30 Mar 2024
Last updated
31 May 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
No

Publications

  • Cluver CA, Hiscock R, Decloedt EH, Hall DR, Schell S, Mol BW, Brownfoot F, Kaitu'u-Lino TJ, Walker SP, Tong S. Use of metformin to prolong gestation in preterm pre-eclampsia: randomised, double blind, placebo controlled trial. BMJ. 2021 Sep 22;374:n2103. doi: 10.1136/bmj.n2103.

    PubMed 34551918
  • Kaitu'u-Lino TJ, Brownfoot FC, Beard S, Cannon P, Hastie R, Nguyen TV, Binder NK, Tong S, Hannan NJ. Combining metformin and esomeprazole is additive in reducing sFlt-1 secretion and decreasing endothelial dysfunction - implications for treating preeclampsia. PLoS One. 2018 Feb 21;13(2):e0188845. doi: 10.1371/journal.pone.0188845. eCollection 2018.

    PubMed 29466360
  • Rowan JA, Hague WM, Gao W, Battin MR, Moore MP; MiG Trial Investigators. Metformin versus insulin for the treatment of gestational diabetes. N Engl J Med. 2008 May 8;358(19):2003-15. doi: 10.1056/NEJMoa0707193.

    PubMed 18463376

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Metformin and Esomeprazole in people with Preeclampsia Severe and Pre-Eclampsia, run by Christiana Care Health Services at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 31 May 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study was stopped early (reason given: Lost funding). Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Mean plasma difference in sFlt-1 (time frame: Over the first 14 days after randomization and during the remainder of pregnancy, an average of 3-4 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06359015, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 31 May 2025.

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