Pilot Study of the SENSITIVE Care Program for Preterm Infants in the Neonatal Intensive Care Unit
NCT07728760
Female Urogenital Diseases and Pregnancy Complications, Infant, Premature
Bantul, DI. Yogyajarta, Indonesia
View Trial DetailsNCT Number: NCT02738411
The main objective of this research is to study the links between changes in the intestinal microbiota (in terms of diversity) during the first 6 weeks of life for preterm infants and the presence / absence of a TH1 immune status at 36 months of age.
Looking for future studies?
Notify MeUp to 1 day
All sexes
Observational
CHRU de Montpellier - Hôpital Arnaud de Villeneuve, Montpellier, France
The secondary objectives are to study the links between changes of the intestinal microbiota premature infants in terms of:
-AND-
The links between certain variables known in the literature and neonatal microbiota will be confirmed / studied in our population:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 36 months
Immune orientation will be determined according to the following ratio determined by lymphocyte stimulation tests: INF-gamma/(INF-gamma+IL+4). The latter ratio varies between 0 and 0.5 with IL-4 > INF-gamma (TH2 orientation) and between 0.5 and 1 when INF-gamma > IL-4 (TH1 orientation).
Time frame: 36 months
Subsets are determined according to the presence/absence of the following differentiation clusters: CD3, CD4, CD8, CD19, CD25, CD56, CD127, FOXP3.
Time frame: 36 months
Time frame: 36 months
Time frame: 36 months
Time frame: 36 months
Time frame: 36 months
Time frame: Day 0 (first meconium)
Time frame: Week 1
Time frame: Week 2
Time frame: Week 3
Time frame: Week 4
Time frame: Week 5
Time frame: Week 6
Time frame: 12 months
Time frame: 24 months
Time frame: 36 months
Time frame: Day 0 (first meconium)
Time frame: Week 1
Time frame: Week 2
Time frame: Week 3
Time frame: Week 4
Time frame: Week 5
Time frame: Week 6
Time frame: 12 months
Time frame: 24 months
Time frame: 36 months
Time frame: Day 0 (first meconium)
Functional groups are determined via the classification of each OTU according to the following factors: 1) pathogenicity (pathogen/intermediate/commensal); 2) aerobic versus anaerobic; 3) Cocci + versus others.
Time frame: Week 1
Functional groups are determined via the classification of each OTU according to the following factors: 1) pathogenicity (pathogen/intermediate/commensal); 2) aerobic versus anaerobic; 3) Cocci + versus others.
Time frame: Week 2
Functional groups are determined via the classification of each OTU according to the following factors: 1) pathogenicity (pathogen/intermediate/commensal); 2) aerobic versus anaerobic; 3) Cocci + versus others.
Time frame: Week 3
Functional groups are determined via the classification of each OTU according to the following factors: 1) pathogenicity (pathogen/intermediate/commensal); 2) aerobic versus anaerobic; 3) Cocci + versus others.
Time frame: Week 4
Functional groups are determined via the classification of each OTU according to the following factors: 1) pathogenicity (pathogen/intermediate/commensal); 2) aerobic versus anaerobic; 3) Cocci + versus others.
Time frame: Week 5
Functional groups are determined via the classification of each OTU according to the following factors: 1) pathogenicity (pathogen/intermediate/commensal); 2) aerobic versus anaerobic; 3) Cocci + versus others.
Time frame: Week 6
Functional groups are determined via the classification of each OTU according to the following factors: 1) pathogenicity (pathogen/intermediate/commensal); 2) aerobic versus anaerobic; 3) Cocci + versus others.
Time frame: 12 months
Functional groups are determined via the classification of each OTU according to the following factors: 1) pathogenicity (pathogen/intermediate/commensal); 2) aerobic versus anaerobic; 3) Cocci + versus others.
Time frame: 24 months
Functional groups are determined via the classification of each OTU according to the following factors: 1) pathogenicity (pathogen/intermediate/commensal); 2) aerobic versus anaerobic; 3) Cocci + versus others.
Time frame: 36 months
Functional groups are determined via the classification of each OTU according to the following factors: 1) pathogenicity (pathogen/intermediate/commensal); 2) aerobic versus anaerobic; 3) Cocci + versus others.
Time frame: Day 0 (first meconium)
Functional groups are determined via the classification of each OTU according to the following factors: 1) pathogenicity (pathogen/intermediate/commensal); 2) aerobic versus anaerobic; 3) Cocci + versus others.
Time frame: Week 1
Functional groups are determined via the classification of each OTU according to the following factors: 1) pathogenicity (pathogen/intermediate/commensal); 2) aerobic versus anaerobic; 3) Cocci + versus others.
Time frame: Week 2
Functional groups are determined via the classification of each OTU according to the following factors: 1) pathogenicity (pathogen/intermediate/commensal); 2) aerobic versus anaerobic; 3) Cocci + versus others.
Time frame: Week 3
Functional groups are determined via the classification of each OTU according to the following factors: 1) pathogenicity (pathogen/intermediate/commensal); 2) aerobic versus anaerobic; 3) Cocci + versus others.
Time frame: Week 4
Functional groups are determined via the classification of each OTU according to the following factors: 1) pathogenicity (pathogen/intermediate/commensal); 2) aerobic versus anaerobic; 3) Cocci + versus others.
Time frame: Week 5
Functional groups are determined via the classification of each OTU according to the following factors: 1) pathogenicity (pathogen/intermediate/commensal); 2) aerobic versus anaerobic; 3) Cocci + versus others.
Time frame: Week 6
Functional groups are determined via the classification of each OTU according to the following factors: 1) pathogenicity (pathogen/intermediate/commensal); 2) aerobic versus anaerobic; 3) Cocci + versus others.
Time frame: 12 months
Functional groups are determined via the classification of each OTU according to the following factors: 1) pathogenicity (pathogen/intermediate/commensal); 2) aerobic versus anaerobic; 3) Cocci + versus others.
Time frame: 24 months
Functional groups are determined via the classification of each OTU according to the following factors: 1) pathogenicity (pathogen/intermediate/commensal); 2) aerobic versus anaerobic; 3) Cocci + versus others.
Time frame: 36 months
Functional groups are determined via the classification of each OTU according to the following factors: 1) pathogenicity (pathogen/intermediate/commensal); 2) aerobic versus anaerobic; 3) Cocci + versus others.
Time frame: Day 0 (first meconium)
Time frame: Week 1
Time frame: Week 2
Time frame: Week 3
Time frame: Week 4
Time frame: Week 5
Time frame: Week 6
Time frame: 12 months
Time frame: 24 months
Time frame: 36 months
Time frame: Day 0 (first meconium)
Time frame: Week 1
Time frame: Week 2
Time frame: Week 3
Time frame: Week 4
Time frame: Week 5
Time frame: Week 6
Time frame: 12 months
Time frame: 24 months
Time frame: 36 months
Centre Hospitalier Universitaire de Nīmes
Other
Influence of Intestinal Microbiota Implantation Parameters in the Neonatal Period in Premature Infants on Microbiota Profiles and Immune Orientation at 3 Years of Age
Acronym: PrimiBiota
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07728760
Female Urogenital Diseases and Pregnancy Complications, Infant, Premature
Bantul, DI. Yogyajarta, Indonesia
View Trial DetailsNCT02863978
Female Urogenital Diseases and Pregnancy Complications, Infant, Premature
Brest, Brittany Region, France
View Trial DetailsNCT05782569
Female Urogenital Diseases and Pregnancy Complications, Infant, Premature
Middlesbrough, United Kingdom
View Trial DetailsNCT07533721
Bronchopulmonary Dysplasia, Cardiovascular Abnormalities
Shenyang, Liaoning, China
View Trial Details