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Autophagy/Apoptosis Balance During Pregnancy (GROSSAUTOP)

C

Centre Hospitalier Universitaire de Nīmes

Status

Completed

Conditions

Pregnancy Related

Treatments

Other: Blood test

Study type

Observational

Funder types

Other

Identifiers

NCT04443660
NIMAO/2019-01/SB-01

Details and patient eligibility

About

The object of this study is to assess the intra- and inter-individual variability of apoptosis and autophagy activities in women during pregnancy: 1 / in women with a normal pregnancy and 2 / in pregnant women particularly at risk of complications.

The study investigators hypothesize that there would be an intra-trophoblastic dialogue between the mechanisms of autophagy and apoptosis, the promotion of one partially inhibiting the other. The increase in trophoblastic autophagy during pregnancy could thus constitute an anti-apoptosis defense phenomenon, the exhaustion of which would lead to cellular apoptosis and to pathogenic consequences when it devastates the syncytiotrophoblast.

Enrollment

97 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients followed at the CHU Nimes prior to 33 weeks gestation who give birth at the hospital
  • The patient must have given their free and informed consent and signed the consent form
  • The patient must be a member or beneficiary of a health insurance plan

Exclusion criteria

  • The subject is participating in a category 1 interventional study associated with a medication, or is in a period of exclusion determined by a previous study
  • The subject refuses to sign the consent
  • It is impossible to give the subject informed information
  • The patient is under safeguard of justice or state guardianship
  • Multiple pregnancy

Trial design

97 participants in 4 patient groups

Group A
Description:
without medical history or risk factors, with a normal pregnancy
Treatment:
Other: Blood test
Group B
Description:
without medical history or risk factors, developing a pregnancy complication
Treatment:
Other: Blood test
Group C
Description:
with risk of complication, having a normal pregnancy
Treatment:
Other: Blood test
Group D
Description:
with a risk of complication, developing a pregnancy complication
Treatment:
Other: Blood test

Trial contacts and locations

1

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Central trial contact

Sylvie Bouvier

Data sourced from clinicaltrials.gov

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