NCT07273643

Brief Summary

This study aims to understand the role of extracellular vesicles (EVs) in extremely premature infants, those born before 28 weeks of gestation. EVs are tiny particles released by cells that carry important information about the body's condition. In extremely premature infants, blood vessels may not function properly, leading to serious health problems such as bleeding in the brain, lung injury, or severe infections. Researchers believe that analyzing EVs in the umbilical cord blood of these infants may help predict which babies are at higher risk of developing these complications. By studying the size, number, and type of EVs, the team hopes to identify early markers that can guide doctors in providing better care. The study will collect cord blood from 30 eligible infants born at the CHU of Montpellier. Blood samples will be processed to isolate platelet-poor plasma, which contains EVs. This plasma will be stored in a biobank, allowing future research on EVs and their role in extreme prematurity. EVs will then be analyzed in the laboratory to assess their characteristics and any links to severe health issues. The findings from this study could improve understanding of circulatory problems in extremely premature infants, help identify early predictors of severe complications, and inform better monitoring and treatment strategies. The creation of a plasma biobank also provides a valuable resource for future research to enhance care and outcomes for this vulnerable population.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for all trials

Timeline
17mo left

Started Jan 2026

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress18%
Jan 2026Oct 2027

First Submitted

Initial submission to the registry

November 19, 2025

Completed
20 days until next milestone

First Posted

Study publicly available on registry

December 9, 2025

Completed
1 month until next milestone

Study Start

First participant enrolled

January 13, 2026

Completed
1.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 13, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 13, 2027

Last Updated

February 23, 2026

Status Verified

February 1, 2026

Enrollment Period

1.7 years

First QC Date

November 19, 2025

Last Update Submit

February 19, 2026

Conditions

Keywords

ELGANExtremely Low Gestational Age Newborn (ELGAN)Extracellular vesiclesEVsIntraventricular hemorragePulmonary hemorrhageBronchopulmonary Dysplasia

Outcome Measures

Primary Outcomes (1)

  • Correlation between occurence of early severe morbidity mortality and characterization of Extracellular vesicles (EVs)

    The primary outcome is the correlation between occurence of early severe morbidity mortality and the characterization of Extracellular vesicles (EVs) for venous cord blood plasma : 1. EV were isolated from venous cord blood plasma using sequential centrifugation and ultracentrifugation steps. EVs were then characterized for size (nm) and concentration (EVs/µL) using a Zetasizer, and their cellular origin was determined by nanocytometry. 2. Early severe morbidity or mortality during the hospital stay is defined as the occurrence of at least one of the following events: * Refractory shock (requiring fluid resuscitation or vasopressor support) * Pulmonary Hemorrhage * Severe Intraventricular Hemorrhage (grade 3 or 4, Papille classification) * Death before discharge

    Blood collection: at birth Centrifugation: within 3 hours of collection. EV isolation and analysis: up to there month after collection. Clinical informations(occurence of early severe morbidity and mortality): through study completion, up to 1year

Secondary Outcomes (3)

  • Correlation between occurrence of other morbidity before discharge and the EVs characterization

    Blood collection: at birth Centrifugation: within 3 hours of collection. EV isolation and analysis: up to there month after collection. Clinical informations (occurence of other morbidity): through study completion, up to 1year.

  • Correlation between obstetric characteristics and causes of prematurity and characterization of venous cord blood EVs.

    Blood collection: at birth Centrifugation: within 3 hours of collection. EV isolation and analysis: up to there month after collection. Clinical informations (obstetric characteristics and causes of prematurity): through study completion, up to 1year

  • Comparison of Arterial and Venous Extracellular Vesicles

    Blood collection: at birth Centrifugation: within 3 hours of collection. EV isolation and analysis: up to there month after collection.

Study Arms (2)

Extremely Low Gestational Age Newborns without severe morbidity or mortality

Extremely Low Gestational Age Newborns (ELGANs) born at Montpellier Hospital before 28 weeks of gestation, who were admitted to the neonatal unit, had cord blood collected at birth, and did not experience severe morbidity (early shock, intraventricular hemorrhage, or pulmonary hemorrhage) or death before discharge.

Biological: Venous Cord blood sampleBiological: Arterial cord blood sample

Extremely Low Gestational Age Newborns with severe morbidity or mortality

Extremely Low Gestational Age Newborns (ELGANs) born at Montpellier Hospital before 28 weeks of gestation, who were admitted to the neonatal unit, had cord blood collected at birth, and experienced severe morbidity (early shock, intraventricular hemorrhage, or pulmonary hemorrhage) or death before discharge.

Biological: Venous Cord blood sampleBiological: Arterial cord blood sample

Interventions

Venous cord blood sample will be collected at birth (10 mL; if not possible, a minimum of 3 mL) from the umbilical vein into an EDTA tube. Plasma was isolated from blood cells by two centrifugation steps. Extracellular vesicles (EVs) were then isolated from plasma using additional centrifugation and ultracentrifugation steps. EVs were sized and counted using a Zetasizer, and their cellular origin was characterized by nanocytometry.

Also known as: EVs extraction and characterization, Blood centrifugation
Extremely Low Gestational Age Newborns with severe morbidity or mortalityExtremely Low Gestational Age Newborns without severe morbidity or mortality

Arterial cord blood sample will be collected at birth (10 mL; if not possible, a minimum of 3 mL) from the umbilical vein into an EDTA tube for the five first inclusions (succeed). Plasma was isolated from blood cells by two centrifugation steps. Extracellular vesicles (EVs) were then isolated from plasma using additional centrifugation and ultracentrifugation steps. EVs were sized and counted using a Zetasizer, and their cellular origin was characterized by nanocytometry.

Also known as: EVs extraction and characterization, Blood centrifugation
Extremely Low Gestational Age Newborns with severe morbidity or mortalityExtremely Low Gestational Age Newborns without severe morbidity or mortality

Eligibility Criteria

Age0 Days - 3 Months
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)
Sampling MethodNon-Probability Sample
Study Population

All live-born infants born before 28 weeks of gestation (extremely preterm) who were hospitalized at Montpellier University Hospital during the inclusion period and had cord blood collected immediately after birth.

You may qualify if:

  • Mother over 18 years old, able to speak and understand French
  • Newborn less than 28 weeks of gestation, born and hospitalized at Montpellier University Hospital
  • Umbilical cord venous blood collected immediately after birth (from the segment between the cord clamp and the placenta), with a volume of 10 ml (which can be reduced to 3 ml if collection is difficult) into an EDTA tube.
  • Parental non-opposition to the study obtained before sample collection

You may not qualify if:

  • Stillborn infant
  • Handling failure: failure to collect the sample or start the first centrifugation more than 3 hours after birth

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CHU de Montpellier

Montpellier, France

RECRUITING

Related Publications (39)

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    PMID: 29503814BACKGROUND

Biospecimen

Retention: SAMPLES WITHOUT DNA

Blood samples will be centrifuged to remove blood cells and obtain plasma, which will be frozen for later analysis of extracellular vesicles (EVs). These samples will be stored for at least five years. Future studies, such as microRNA analysis, functional tests, or microscopic visualization, may also be performed. All of this sample will be anonymized.

MeSH Terms

Conditions

DeathBronchopulmonary DysplasiaShockEnterocolitis, Necrotizing

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and SymptomsVentilator-Induced Lung InjuryLung InjuryLung DiseasesRespiratory Tract DiseasesInfant, Premature, DiseasesInfant, Newborn, DiseasesCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesEnterocolitisGastroenteritisGastrointestinal DiseasesDigestive System DiseasesIntestinal Diseases

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Target Duration
3 Months
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 19, 2025

First Posted

December 9, 2025

Study Start

January 13, 2026

Primary Completion (Estimated)

October 13, 2027

Study Completion (Estimated)

October 13, 2027

Last Updated

February 23, 2026

Record last verified: 2026-02

Locations