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Levels of Visfatin/NAMPT in Human Milk

Levels of Visfatin/NAMPT in Human Milk.VISFAMILK

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06487286
Acronym
VISFAMILK
Enrollment
30
Registered
2024-07-05
Start date
2024-10-24
Completion date
2025-04-23
Last updated
2024-11-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Birth Weight, Visfatin Levels in Maternal Milk Samples

Keywords

Newborns, Visfatin, Breastfeeding

Brief summary

Visfatin, released in maternal milk at different concentrations related to the maternal conditions, could act as a biomarker with a prognostic/predictive value to determine different newborn clinical conditions, particularly the weight loss of the neonate.

Detailed description

The aim of the study is to analyse a retrospective cohort of well characterized mothers in their post-partum period, and to measure Visfatin levels through collection of maternal milk samples. They will be collected in three different moments after the birth (48 hours, 7 days and 30 days) and Visfatin levels will be analysed through an ELISA kit Adipogen. In parallel, the levels of Visfatin will be evaluated in the maternal plasma/serum collected after 1-2 days postpartum. Lastly, correlations between Visfatin levels and biological/clinical features of mothers and newborns will be explored.

Interventions

OTHERobservational study

observational study

Sponsors

Università degli Studi del Piemonte Orientale Amedeo Avogadro
CollaboratorOTHER
Paolo Manzoni Study Group
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Healthy male and female infants born after 37 weeks' gestation who do not have conditions related to congenital abnormalities * Maternal hospitalization * Acquisition of the informed consent form signed by the patient

Exclusion criteria

* Refusal of the patient to participate in the study * Presence of hypogalactia or agalactia in the patient

Design outcomes

Primary

MeasureTime frameDescription
Visfatin levels48 hours, 7 days and 30 daysVisfatin levels in maternal milk samples

Secondary

MeasureTime frameDescription
values of Visfatin6 monthscorrelate the values of Visfatin to different demographic and clinical characteristics of the lactating mothers

Countries

Italy

Contacts

Primary ContactPaolo Manzoni, Professor
paolo.manzoni@aslbi.piemonte.it+39 01515156906

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026