Study on Sildenafil and Hypothermia for Newborns with Hypoxic-Ischemic Encephalopathy

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What is this study about?

This clinical trial is focused on studying a condition known as hypoxic-ischemic encephalopathy in newborns. This condition occurs when a baby’s brain doesn’t receive enough oxygen and blood, which can lead to brain damage. The study will explore the effects of a treatment combining sildenafil and controlled cooling, also known as hypothermia, to see if it can improve survival without brain injuries. Sildenafil is a medication that is being tested in this study in the form of a solution for injection.

The purpose of the study is to determine if the combination of sildenafil and hypothermia is more effective than hypothermia alone. The study will be conducted in two steps. In the first step, researchers will examine how the body processes sildenafil in newborns with the condition. In the second step, the study will compare the outcomes of newborns receiving the combination treatment to those receiving a placebo, focusing on survival without brain lesions as seen on an MRI scan at the time of hospital discharge.

Throughout the study, researchers will monitor various aspects of the newborns’ health, including brain activity and heart function, to assess both the potential benefits and safety of the treatment. The study aims to provide valuable insights into whether this treatment approach can help improve outcomes for newborns affected by hypoxic-ischemic encephalopathy.

1 joining the trial

Upon joining the trial, the neonate must be born at or after 36 weeks of gestation and diagnosed with hypoxic ischemic encephalopathy (HIE).

The neonate will be treated with therapeutic hypothermia, which involves maintaining a body temperature of 33.5 ± 0.5 °C.

2 beginning treatment

The experimental treatment will start after more than 1 hour of active hypothermia and within the first 12 hours of life.

The neonate will receive sildenafil intravenously, which is a solution for injection, as part of the treatment.

3 monitoring and assessments

During the trial, the primary focus will be on measuring the plasma concentrations of sildenafil to understand how the body processes the medication.

The neonate’s survival without brain lesions will be assessed using an MRI scan between the end of rewarming (day 3.5) and day 5.

4 secondary assessments

Additional assessments will include changes in EEG patterns, detailed analysis of MRIs, and spectroscopy.

A 2-year follow-up will assess neurodevelopmental outcomes, including potential autism spectrum disorders.

5 safety evaluations

Safety evaluations will include monitoring for low systemic pressure that may require support and assessing cardiac function.

Who Can Join the Study?

  • Newborns born at or after 36 weeks of pregnancy.
  • Newborns treated with a special cooling treatment called therapeutic servo-controlled hypothermia (temperature set at 33.5 ± 0.5 °C) for a condition known as neonatal HIE.
  • The experimental treatment will start more than 1 hour after the cooling treatment begins and less than 12 hours after birth.
  • The newborn must have social security coverage.
  • One of the parents or legal guardians must provide written consent for the newborn to participate in the study.

Who Cannot Join the Study?

  • Patients with conditions other than Hypoxic Ischemic Encephalopathy (a type of brain injury caused by lack of oxygen).
  • Patients who are not newborns (neonates) born after 36 weeks of pregnancy.
  • Patients who are not undergoing treatment with controlled cooling (hypothermia).
  • Patients who are not eligible for treatment with IV sildenafil (a medication used in this study).

Where you can join this trial?

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Other Sites

Site Name City Country Status
Hopital Beaujon Clichy France

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
France France
Not yet recruiting
01.09.2024

Trial locations

Investigated drugs:

Sildenafil is a medication that is being studied in this trial for its potential benefits in newborns with a condition called hypoxic-ischemic encephalopathy (HIE). This condition occurs when a baby’s brain does not receive enough oxygen and blood. In this trial, sildenafil is given through an IV, which means it is administered directly into the bloodstream. The researchers want to see if sildenafil can help improve the chances of survival without brain damage when used alongside a treatment called controlled hypothermia. Controlled hypothermia is a therapy where the baby’s body temperature is lowered to help protect the brain from further injury.

Hypoxic ischemic encephalopathy – This condition occurs when the brain does not receive enough oxygen and blood flow, often around the time of birth. It can lead to brain cell damage due to the lack of oxygen and nutrients. The progression of the disease can vary, with some infants experiencing mild effects and others facing more severe neurological issues. Initially, symptoms may include difficulty breathing, poor muscle tone, and seizures. Over time, affected infants may develop problems with movement, learning, and other developmental milestones. The severity of these issues depends on the extent of the initial brain injury.

Trial ID:
2023-508928-35-00
Protocol code:
APHP180603
Trial Phase:
Therapeutic use (Phase IV)

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