Study on Doxapram for Treating Apnea in Preterm Newborns

3 1

What is this study about?

This clinical trial is focused on studying a condition known as apnea of prematurity, which affects newborns who are born too early, also known as preterm infants. The trial is investigating a treatment using a medication called doxapram, which is given as a solution through an intravenous infusion. The purpose of the study is to determine if doxapram is safe and effective in reducing the risk of death and severe developmental problems in these infants when compared to a placebo.

During the study, preterm newborns will receive either doxapram or a placebo. The treatment will be administered over a period of time, and the infants will be monitored closely by healthcare professionals. The study aims to observe the effects of the treatment on the infants’ health and development up to the age of 18 to 24 months.

The trial is designed to provide valuable information on whether doxapram can help improve outcomes for preterm infants with apnea of prematurity. By comparing the results between those receiving doxapram and those receiving a placebo, researchers hope to gain insights into the potential benefits and safety of this treatment for vulnerable newborns.

1 joining the study

The study involves preterm newborns with a gestational age at birth of less than 29 weeks.

The newborn must be admitted to the Neonatal Intensive Care Unit (NICU) of a participating center.

Written informed consent is required from the parent(s) or legal representatives according to national guidelines.

2 eligibility confirmation

The newborn must be at least 120 hours old postnatally.

The newborn should be receiving caffeine therapy at an adequate dose.

Optimal non-invasive respiratory support should be provided according to local treatment policy, which may include nasal CPAP or ventilation methods such as (S)NIPPV, BIPAP/Duopap, or nasal HFO.

The newborn must experience frequent and/or severe apneas that require medical intervention as judged by the attending physician.

3 treatment administration

The trial involves the administration of doxapram hydrochloride monohydrate or a placebo.

The medication is given intravenously as a solution for infusion.

The specific dosage and frequency of administration are determined by the study protocol and the attending medical team.

4 monitoring and follow-up

The primary outcome of the trial is to assess the composite outcome of death or severe disability at the age of 18-24 months corrected age.

Both outcomes will also be analyzed separately to determine the safety and effectiveness of doxapram compared to placebo.

5 trial completion

The estimated end date for the trial is April 1, 2027.

The results will contribute to understanding the safety and effectiveness of doxapram in reducing severe outcomes in preterm newborns.

Who Can Join the Study?

Admitted to the NICU (Neonatal Intensive Care Unit) of one of the participating centers
Written informed consent according to the national guidelines of both (the Netherlands) or at least one (Belgium and Canada) parent(s) or legal representatives
Born with a gestational age of less than 29 weeks (gestational age is the time period from the first day of the mother’s last menstrual cycle to the current date, measured in weeks)
At least 120 hours old after birth
Receiving caffeine therapy with the correct dosage (caffeine therapy is a treatment used to help stimulate breathing in premature babies)
Receiving the best possible non-invasive breathing support according to local treatment policy, which may include nasal CPAP or ventilation methods like (S)NIPPV, BIPAP/Duopap, or nasal HFO (these are different types of breathing support that help babies breathe without needing a tube in their windpipe)
Experiencing frequent and/or severe apneas that need medical intervention as decided by the attending doctor (apnea is a condition where breathing stops for a short period)

Who Cannot Join the Study?

Patients who have a known allergy or adverse reaction to the study medication.
Patients with a medical condition that the study doctors believe would make it unsafe for them to participate.
Patients who are currently participating in another clinical trial.
Patients who have a history of a serious heart condition.
Patients who have a history of severe liver or kidney disease.
Patients who are unable to follow the study procedures as required.
Patients who are pregnant or breastfeeding.
Patients who have a history of drug or alcohol abuse.
Patients who have a condition that affects their ability to understand the study and provide consent.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name	City	Country
University Hospital Maastricht	Maastricht	The Netherlands
Katholieke Universiteit te Leuven	Leuven	Belgium
Université Libre de Bruxelles – Hôpital Erasme	Brussels	Belgium

Other Sites

Site Name	City	Country
Isala Klinieken Stichting	Zwolle	The Netherlands
Grand Hopital De Charleroi	Charleroi	Belgium
Chirec	Brussels	Belgium
Maxima Medisch Centrum	Veldhoven	The Netherlands
Universitair Medisch Centrum Utrecht	Utrecht	The Netherlands
Az St-Jan Brugge-Oostende A.V.	Brugge	Belgium
Stichting Radboud University Medical Center	Nijmegen	The Netherlands
Gasthuiszusters Antwerpen	Antwerp	Belgium
Ziekenhuis Oost Limburg	Genk	Belgium
Vrije Universiteit Brussel	Jette	Belgium
Cejstoavq Uqvskgistpewqm Snhqvjbqq	Woluwe-Saint-Lambert	Belgium
Lxika Ufvceypnjdpe Mjrlsqq Cqqzgpr (lrwiz	Leiden	The Netherlands
Uowchhtyefwt Mjmdxri Csccnou Gxfkesjhv	Groningen	The Netherlands
Aqrkxqtoh Ult	Amsterdam	The Netherlands
Ekywpsd Usqrbpdgxins Mxcfans Cifhdxq Rjeuzhwfe (pmrboll Mca	Rotterdam	The Netherlands
Uolwmgvzzm On Akjnlpp	Edegem	Belgium

Trial status

Country	Status	Recruitment Start
Belgium	Recruiting	01.04.2020
The Netherlands	Recruiting	01.04.2020

Trial locations

Doxapram is a medication being studied to see if it is safe and effective for use in preterm newborns. The trial aims to determine if it can help reduce the risk of death and neurodevelopmental problems or severe disabilities in these infants when they reach 18 to 24 months of corrected age.

Investigated diseases:

Infantile apnoea

Apnea of Prematurity – This condition occurs in premature infants and is characterized by pauses in breathing for more than 20 seconds. These pauses can be accompanied by a decrease in heart rate and a drop in blood oxygen levels. It is primarily due to the immaturity of the respiratory control centers in the brain. The condition is most common in infants born before 34 weeks of gestation. As the infant matures, the frequency and severity of apnea episodes typically decrease. Most infants outgrow this condition as their respiratory system develops.

Trial ID:

2024-515625-29-00

Protocol code:

NL72125.078.19

NCT ID:

NCT04430790

Trial Phase:

Therapeutic confirmatory (Phase III)

Other Trials to Consider

#1 Clinical Trials Search in Europe

Study on Doxapram for Treating Apnea in Preterm Newborns

What is this study about?

Who Can Join the Study?

Who Cannot Join the Study?