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Study identifier: NCT07358026 Synced from ClinicalTrials.gov · July 28, 2026
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EARLY-PREG: A Preconception Cohort Study Based on Counterfactuals to Study Maternal-Embryonic Molecular Interactions

Condition: Early Pregnancy · Early Pregnancy Loss · Childbirth  ·  Sponsor: MELISA Institute Genomics & Proteomics Research SpA

PhaseN/A
Planned participants223
Who can joinFemale, 18 Years to 40 Years
Healthy volunteersYes

About this study

EARLY-PREG is an open-cohort clinical study with a preconception, longitudinal, bidirectional and counterfactual design. The aim of this cohort is to investigate the proteomic signatures of maternal-embryonic communication by interrogating a growing biorepository of maternal fluids and tissues collected during the first two weeks after fertilisation. Participants in the EARLY-PREG cohort consist of healthy couples seeking pregnancy, as well as women who are not seeking to conceive. The three main outcomes in the cohort are defined according to menstrual cycles in which conception is achieved and those in which conception is not achieved. Their clinical definitions are as follows: * Pregnancy with a full-term live birth refers to the cycle in which the ovum is fertilised, leading to pregnancy, with beta-hCG levels above the clinical threshold for a positive pregnancy test. * Early pregnancy loss refers to a miscarriage up to 12 6/7 weeks. * Non-pregnancy refers to a menstrual cycle in which conception does not occur, confirmed by a clinically negative beta-hCG test. When referring to the same individual, this is, by definition, considered the counterfactual to the corresponding conception cycle.

This description comes directly from the study's public registry record.

Talk to the study team

Elard S Koch  ·  +56 41 246 7242  ·  ekoch@melisainstitute.org

Patricio A Alcaino  ·  +56 41 246 7242  ·  palcaino@melisainstitute.org

Always discuss trial participation with your own doctor first.

Locations (1)

Clínica Sanatorio AlemánChiguayante, ChileRecruiting

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Source record: clinicaltrials.gov/study/NCT07358026