Clinical trial Recruiting at 1 site Observational Ages 18 and up Women only

Cadmium Exposure in Pregnancy and Its Effect on Fetal Growth

Official title: Cadmium Exposure During Pregnancy and Fetal Growth

Run by Centre Hospitalier Universitaire, Amiens · NCT07855237 · Data updated 2026-11-12

This observational study follows pregnant people to see how cadmium exposure relates to fetal growth and birth weight.

Quick facts

Study typeObservational
Ages18 Years and up
SexWomen only
Enrollment50 (estimated)
SponsorCentre Hospitalier Universitaire, Amiens
Academic / other
Locations1 site (Amiens)
StatusRecruiting
StartedSeptember 21, 2026
Main results expectedNovember 2026
Study endsDecember 2026
Registry record updatedNovember 2, 2026
Trial IDNCT07855237 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Pregnant women aged 18 or older with singleton pregnancies planning delivery at CHU Amiens, who can provide informed consent under French non-interventional research rules.

Probably not a fit

Participants with low cadmium exposure or whose outcomes are not affected by exposure levels may not experience direct benefits.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This non-interventional study collects maternal blood, urine, and placental tissue to measure cadmium exposure during pregnancy and to examine associations with placental function and fetal growth. It leverages a single-center population at CHU Amiens in France and uses observational methods to relate exposure levels to birth outcomes. The study provides biomonitoring data and aims to understand exposure pathways and potential risks to neonatal health. No experimental treatment is given; the effort focuses on observational correlations in a real-world setting.

Why it matters

Potential benefit: Findings could improve understanding of how cadmium exposure affects fetal growth and inform public health strategies to reduce risk.

How similar studies have gone: Previous research has linked placental cadmium exposure to adverse fetal outcomes, supporting the relevance of this observational approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Pregnant women aged 18 years or older
* Singleton pregnancy
* Planned delivery at the maternity unit of Amiens University Hospital (CHU Amiens)
* Ability to receive study information and provide informed non-opposition/consent according to French regulations for non-interventional research

Exclusion Criteria:

* Women under legal protection measures, including guardianship, curatorship, or judicial safeguard
* Inability to understand the study objectives or the constraints of the protocol (language barrier, cognitive impairment, or other reasons)
* Lack of affiliation to a social security system, as required by French regulations

Where it's running

  • CHU Amiens Picardie
    Amiens, France
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.