Kynurenine Concentrations During Pregnancy in Women With or Without Chronic Kidney Disease - A Prospective Multicenter Study

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorCHU de Reims

About this trial

Chronic kidney disease (CKD) affects more than 10% of the population worldwide and represents the second most important risk factor for preeclampsia, a life-threatening complication of pregnancy responsible for approximately 80,000 maternal and 500,000 perinatal deaths each year. Experimental studies have suggested a causal link between CKD, relative kynurenine deficiency during pregnancy, and preeclampsia development. Kynurenine, a tryptophan metabolite, plays a central role at the materno-fetal interface, supporting placental energy production, maternal-fetal immune tolerance, and placental perfusion. This study will prospectively assess and compare longitudinal kynurenine concentrations in pregnant women with and without CKD, and evaluate their associations with maternal and fetal outcomes.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult pregnant women <14 weeks of amenorrhea

With or without CKD stage 2-4 (eGFR 15-89 mL/min/1.73m², diagnosed before pregnancy)

Written informed consent

Affiliation to a social security system

Disqualifiers

Multiple pregnancy

Kidney transplantation

Persons under guardianship or legal protection

Trial design

Design model

Single group

Treatments tested in this trial

  • Blood sampling

    Other intervention

    A 14ml blood sample will be collected during the first second and third trimesters of pregnancy and at 2 months (+ 1 month post partum)

Treatment groups

204 Participants
are divided into 2 treatment groups
Group A: Women with chronic kidney diseaseOther 1 intervention
Group B: Women without chronic kidney diseaseOther 1 intervention

Trial outcomes

Primary outcomes

1

Kynurenine concentration at the 3rd trimester (32±1 weeks) in women with and without CKD

Time frame
32±1 weeks

Secondary outcomes

1

Kynurenine concentrations at 1st, 2nd, 3rd trimesters and 2 months postpartum in women with and without CKD

Time frame
at 9 months
2

preeclampsia

Time frame
at 6 months
3

gestational hypertension

Time frame
at 6 months
4

HELLP syndrome

Time frame
at 6 months

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: