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Clinical Trials/NL-OMON38195
NL-OMON38195
Completed
Not Applicable

Immune development in early life - Immune development in early life

niversitair Medisch Centrum Utrecht0 sites205 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Allergy
Sponsor
niversitair Medisch Centrum Utrecht
Enrollment
205
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational invasive

Investigators

Sponsor
niversitair Medisch Centrum Utrecht

Eligibility Criteria

Inclusion Criteria

  • \- Healthy term (37\-42 weeks) newborns born in the hospital on maternal indication after an uncomplicated pregnancy and delivery
  • \- Diabetes group: Newborns from mothers with diabetes mellitus or diabetes gravidarum at risk for hypoglycaemia and who will routinely have several glucose controls in the first 24\-48 hours after birth
  • \- Sepsis group: Newborns with a clinical diagnosed sepsis
  • \- PCOS group: Newborns from mothers with PCOS
  • \- CMV infection group: Preterm born children (AD\<32 weeks) with a postnatal acquired CMV infection and matched controls with similar clinical and patient characteristics but without a CMV infection

Exclusion Criteria

  • \- Complications during pregnancy (HELLP, pre\-ecmplampsia, infection) except for the pathological conditions under investigation
  • \- Smoking during pregnancy
  • \- Use of immune\-modulating medication during pregnancy
  • \- Use of antibiotics by the mother in two weeks before delivery
  • \- Perinatal complications not related to inclusion criteria
  • \- Prematurity (GA\<36 weeks) or dysmaturity (birth weight \< \-2 SD) except for the preterm born children in the CMV infected population or their controls
  • \- Immunological disorders like velocardiofacial syndrome, DiGeorge syndrome
  • \- Chromosomal disorders

Outcomes

Primary Outcomes

Not specified

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