PRECEE2 Perinatal Research

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

30000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-04-10

Study Completion Date

2026-01-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The aim of this study is to analyze the relationship between complications and adverse pregnancy outcomes and exposure to environmental factors in women living in Franche-Comté who gave birth between 2011 and 2025 at Besancon University Hospital.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Study of the Risk of PREMaturité According to the Balance of Bacterial Flora VAginale

NCT03618836

Preterm Birth

COMPLETED

Air Pollution and Daily Mobility of Pregnant Women Identification of Critical Windows of Exposure

NCT04725734

Pregnancy Low Birth Weight Preterm Birth +1 more

UNKNOWN

Is a History of Pre-eclampsia a Risk Factor for Vascular Phenotype in Women With Systemic Sclerosis?

NCT04363021

Systemic Sclerosis Preeclampsia Vascular Complications

COMPLETED

Study of the Physiology of Pre-eclampsia and Vascular IUGR With Constitution of a Biological Collection

NCT03626233

Pre-Eclampsia

UNKNOWN

Interest of Measuring Lung Elasticity ELASTOgraphy in the Fetus in the Case of PreMAture Childbirth Threat

NCT02870608

Pregnancy Complications Obstetric Labor, Premature

COMPLETED NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Pregnancy Complications

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

OTHER

Study Time Perspective

RETROSPECTIVE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Study on existing health data

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Women who gave birth at the CHUB between 01/01/2011 and 12/31/2025
* who have not expressed any objection to the processing of their data.

Exclusion Criteria

* Legal incapacity or limited legal capacity
* Subject is within the exclusion period of another study or is excluded from the "national volunteer file".
* Subject refusing the collection of his/her medical data.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes