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Attenuated Inflammation and Interferon Release in the Perinatal Phase, TRR359

Attenuated Inflammation and Interferon Release in the Perinatal Phase, TRR359 - PERI-IFN

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00039318
Enrollment
40
Registered
2026-02-11
Start date
2025-12-01
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Healthy Mothers and their newborn children

Interventions

Group 1: Collection of umbilical cord blood and placental tissue from newborns, as well as blood samples from healthy adult donors, followed by the investigation of cellular and molecular differences

Sponsors

Genzentrum der LMU
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Pregnant women: =18 years of age; planned delivery at LMU University Hospital Großhadern; ability to provide informed consent in German or (if offered) English; consent obtained prior to delivery. Newborns: born to the same participant; umbilical cord blood collection after clamping and cutting of the umbilical cord; no study-related intervention performed on the child. Adult controls: =18 years of age; not pregnant; self-reported “healthy” status; ability to provide informed consent; written informed consent.

Exclusion criteria

Exclusion criteria: Minor pregnant women; lack of capacity to provide informed consent; absence of written informed consent. Emergency or precipitous deliveries with medical priority where providing study information is not feasible; severe obstetric complications requiring priority of acute medical care. Acute febrile infections/neutropenia; known relevant immunodeficiencies; systemic immunosuppression (e.g., >10 mg prednisolone equivalent for >14 days); known active autoimmune disease or inflammatory systemic disease. Known highly contagious or notifiable infections with special hygiene requirements (e.g., open tuberculosis, hemorrhagic fevers; standard BSL-2 infections will be processed according to hygiene standards but may be excluded based on resource or safety considerations). Anticoagulation with high bleeding risk or severe anemia (<9 g/dL hemoglobin) for optional maternal blood sampling. For adult controls additionally: current pregnancy; chronic inflammatory or autoimmune disease; ongoing immunosuppressive therapy; acute infection (<14 days).

Design outcomes

Primary

MeasureTime frame
Aim of the study: Mechanistic understanding of perinatal Inflammation and Interferon pathways

Countries

Germany

Contacts

Public ContactJonathan Bohlen

Genzentrum der LMU

j.bohlen@lmu.de+49 89 2180 71055

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 14, 2026