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NCT Number: NCT05002023

PRINCE Study - Cohort Study of Healthy Pregnant Women Followed by the Assessment of Children´s Health and Immunity

In the PRINCE study we recruit healthy but also diseased pregnant women into a cohort study, followed by the assessment of children´s health and immunity at birth and during the first 10 years of life. This unique cohort allows for testing the impact of prenatal challenges on children´s health.

Recruiting

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Key information

Age range

18 year–50 year

Sex eligibility

Female

Study type

Observational

Primary location

Universitätsklinikum Hamburg-Eppendorf

Hamburg, 20246, Germany

Location status: Recruiting

Location contact

Franziska Rüber, MD

CONTACT

About this study

Children´s Health is critically dependent of the prenatal well-being of the mother, and a number of observational studies have identified an impaired immunity in children upon prenatal challenges, such as stress perception, medication, nutrition or infection. However, concerted, in-depth studies assessing how such prenatal challenges may alter fetal development and subsequently children´s health in humans are largely lacking. In the present project, we address this limitation by recruiting healthy, but also diseased pregnant women into a cohort study, followed up by the assessment of children´s health and immunity at birth and during the first ten years of life.

Study participants are recruited early in the first trimester (12-15 weeks of gestation). By means of data security all participants receive a study number. Data processing into the data base (Redcap) is performed under this pseudonym.

During the first visit, the study team explains the enrollment conditions and the participants are asked to give their consent. Study visits include the documentation of clinically important conditions, sonographic examination of the fetus, assessment of mother´s height and weight as well as blood collection (21 ml) of the mother. Additionally we document any kind of medication-intake and nutrition data, and the participants are asked to fill in a psychometric questionnaire. Study visits are scheduled according to the week of gestation, i.e. around 13th, 20th (ultrasound only), 24th, 28th, 34th week. If women give birth in our clinic, we are able to collect cord blood after birth.

Blood samples are processed immediately and stored in our laboratory under Biobank-conditions.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Pregnant women
  • >18 years of age
  • able to understand and sign the papers of consent
  • singleton pregnancy

Exclusion criteria

:

  • <18 years of age
  • unable to give consent
  • multiple pregnancy
  • nicotine abuse
  • fetal aberration

Treatment and study plan

Primary outcomes

  1. Types of allergic diseases in childhood

    Time frame: 10 years follow up

    The different types of allergic diseases are assessed by a yearly questionnaire, a pediatric examination and lung function testing of the child aged 5 and 9 1/2 years, as well as analysing blood samples of the child aged 5 and 9 1/2 years. Main allergies we measure are inhalation allergens and infant food.

Secondary outcomes

  1. influences during pregnancy that potentially affect children´s health

    Time frame: 10 years follow up

    assessed by maternal examination during pregnancy including ultrasound in every trimester

  2. influences during pregnancy that potentially affect children´s health

    Time frame: 10 years follow up

    assessed by questionaire every trimester with questions about nutrition, infections, medication, stress (...)

  3. influences during pregnancy that potentially affect children´s health

    Time frame: 10 years follow up

    assessed by analysing blood samples of the mother in every trimester and analysing cord blood

Study contacts

Contact information is provided by the study sponsor or research team.

Lina Otto

CONTACT

[email protected]

0049 +43 7410-58706

Prof. Dr. Anke Diemert, MD

CONTACT

[email protected]

0049 +40 7410- 57832

Sponsors and collaborators

Lead sponsor

Universitätsklinikum Hamburg-Eppendorf

Other

Registry information

Official study title

PRINCE - PRenatal Identification of Childrens HEalth

Acronym: PRINCE

Important dates

Study start
2011
Primary completion
2050
Study completion
2050
First posted
Aug 12, 2021
Registry last updated
Aug 26, 2021

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.

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