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Prognostic Contribution of Abdominal Ultrasound in Necrotizing Enterocolitis in Preterm Infants Less Than 33SA. (ECUN)

P

Public Assistance-Hospitals of Marseille (AP-HM)

Status

Unknown

Conditions

Preterm Infants
the Necrotizing Enterocolitis

Treatments

Device: Abdominal ultrasound

Study type

Interventional

Funder types

Other

Identifiers

NCT02872350
2015-A01628-41 (Registry Identifier)
2015-34

Details and patient eligibility

About

Enterocolitis necrotizing (ECUN) is a common and serious gastrointestinal disease in premature infants.

The diagnosis of ECUN based on clinical and radiological criteria. The abdomen plain film to date is the reference examination to confirm or refute the diagnosis. Indeed, the presence of pathognomonic signs (pneumatosis, aéroportie) on the abdomen of cliché can confirm the diagnosis. The prognostic value of these radiographic findings is currently controversial.

Abdominal ultrasound is a test whose possibilities in diagnostic and prognostic term began to be considered for some years. It also has other advantages, including that of not being a radiating examination. Studies on the prognostic value of abdominal ultrasound are rather few. Moreover, they involve a series of heterogeneous patients in terms of gestational age. Or the pathophysiology of ECUN in children born at term and in children born prematurely is not the same.

The objective is to study prospectively the prognostic contribution of abdominal ultrasound in the ECUN in premature under 33SA.

Enrollment

95 estimated patients

Sex

All

Ages

Under 33 weeks old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Birth Term strictly less than 33SA
  • Gestational age some (assessed on early ultrasound dating)
  • Congenital malformation of Absence
  • Suggestive clinical symptomatology of ECUN defined by the presence of abdominal bloating, increased residues (> 20% of the volume of enteral feeding) and the presence of blood in stool (macro- or microscopic)
  • Radiologic investigation with a radiograph of abdomen and abdominal ultrasound done for the episode of ECUN
  • Maximum interval between imaging tests 2 hours
  • No parental opposition to the participation of children in the study

Exclusion criteria

  • Term higher or equal to 33 weeks
  • Congenital malformation
  • Parental Opposition (or legal representatives) to participate in the study

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

95 participants in 1 patient group

Premature with necrotizing enterocolitis
Experimental group
Treatment:
Device: Abdominal ultrasound

Trial contacts and locations

1

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Central trial contact

Aurelie GARBI, PH; Urielle DESALBRES, Director

Data sourced from clinicaltrials.gov

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