CRISTEL Study: Monitoring of Pregnancies in Women After Solid Organ Transplantation
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Blood sample.
- Who it may be relevant to
- Registry conditions: Surgical Operation With Transplant of Whole Organ. Basic parameters: 18 years — 48 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
The objective of this research is to obtain standardized and independent data on the number of pregnancies occurring in France and their follow-up up to 1 year postpartum (or post-pregnancy termination). This study will then aim to describe the clinical characteristics and maternal and perinatal outcomes of pregnancies in this specific population. These data will enable the dissemination of clear and up-to-date information to the medical community, thus contributing to better patient counseling and, more broadly, to couples. They will also serve to issue recommendations to optimize the planning and follow-up of pregnancies in women with solid organ transplants. Finally, this initiative aims to promote clinical research on pregnancies.
Detailed description
According to North American and Australian registries, pregnancy is both a joyful and high-risk event for women who have received a solid organ transplant. Typically, a transplanted woman has a probability comparable to that of the general population of giving birth to a live infant, but she is likely to deliver prematurely (median gestational age: 32 weeks), to have a growth-restricted baby (median birth weight around 2.3 kg), and often in a context of preeclampsia (in at least 30% of cases)(1).
Today, these are the data shared with patients planning a pregnancy, despite uncertainty as to their accuracy and applicability in France or even Europe.
Among the unknowns that remain despite these registry data, the following should be noted:
Uncertainty about the level of pregnancy planning in this specific context: What proportion of women of childbearing age have been informed of the possibility of becoming pregnant, of the associated risks, and of necessary precautions (e.g., stopping mycophenolate mofetil at least 6 weeks before conception);
Variability in the information provided from one center to another, due to the absence of a national, consensus-based document addressing fertility and contraception in the post-transplantation setting;
Monitoring frequency specific to the graft, especially regarding exposure to immunosuppressive drugs (and consequently actual exposure to calcineurin inhibitors, the cornerstone of anti-rejection therapy, whose residual blood concentration varies from the second trimester onward)(2);
The true risk of preeclampsia, at a time when diagnosis can be refined by measuring levels of placental-derived anti-angiogenic factors in maternal serum (sFlt-1/PlGF ratio)(3), and by uterine artery Doppler;
The incidence of de novo anti-HLA immunization (HLA antigens expressed by the fetus and inherited from the father), which can now be assessed using the Luminex technique(4);
Maternal morbidity: What is the impact of pregnancy on graft function? Conversely, how does renal function influence pregnancy outcomes, regardless of the transplanted organ?
Infant morbidity in the short and medium term.
To establish these data and to provide accurate information to patients, we aim to conduct a study among pregnant women who have undergone solid organ transplantation (kidney, heart, lung, liver, or pancreas). The objective of this research is to collect standardized and independent data on the number of pregnancies occurring in France and to monitor them up to one year postpartum (or after pregnancy termination).
The study will then aim to describe the clinical characteristics and maternal and perinatal outcomes of pregnancies in this specific population. These data will help disseminate clear and up-to-date information to the medical community, thus improving patient counseling and, more broadly, support for couples. They will also serve to develop recommendations to optimize the planning and management of pregnancies in women with solid organ transplants.
Finally, this initiative aims to promote clinical research on pregnancy in the context of transplantation, particularly through clinical trials and the development of biobanks.
Interventions
- Other Blood sample
Two optional (non-mandatory) biological samples may be collected as part of this study: A 2 mL venous blood sample may be taken during a routine prenatal follow-up visit (around 30 weeks of gestation) in order to analyze the preeclampsia biomarker (sFlt-1/PlGF ratio), whenever preeclampsia is suspected. A 5 mL sample from cord blood may be collected after delivery to analyze, in the newborn, the complete blood count, white blood cell differential, lymphocyte phenotyping (T CD3+, CD19+CD20+, an
Primary outcome measures
- The primary outcome is the annual incidence of conception in the population of women with solid organ transplants (i.e., included in the study). [Time frame: Annually over the 10-year study period]
Secondary outcome measures (12)
- Rate of preeclampsia [Time frame: Through study completion, an average of 1 year]
- Trajectory of estimated glomerular filtration rate (eGFR, in mL/min/1.73 m²); [Time frame: 3 months and 12 months postopartum]
- Live birth rate among transplanted mothers from the onset of pregnancy. [Time frame: through study completion, an average of 1 year]
- Trajectory of serum creatinine levels [Time frame: During pregnancy (up to 40 weeks if gestation)]
- Rate of maternal complications before delivery and in the postpartum period (infectious episodes, rejection episodes, therapeutic pregnancy termination, postpartum hemorrhage) [Time frame: During pregnancy (up to 40 weeks of gestation) and during post partum from delivery up to about 1 year after birth]
- Mode of delivery (spontaneous labor, induced labor, planned cesarean section, or emergency cesarean section); gestational age at delivery (in weeks of gestation); proportion of gestational hypertension and preeclampsia. [Time frame: Day of delivery: Perioperative/Periprocedural]
- Birth weight of the newborn (in grams) [Time frame: day of delivery]
- Rate of spontaneous miscarriage [Time frame: Through study completion, an average of 1 year]
- Rate of cesarean section [Time frame: Through study completion, an average of 1 year]
- Rate of prematurity [Time frame: Through study completion, an average of 1 year]
- Rate of intrauterine growth restriction [Time frame: Through study completion, an average of 1 year]
- the duration of hospital stay for both the mother and the newborn [Time frame: Through study completion, an average of 1 year]
Eligibility criteria
Inclusion criteria
- Female patient aged 18 years or older and of childbearing age
- Has received a solid organ transplant, either isolated or combined (heart, liver, lung, pancreas, kidney)
- Has a positive blood beta-hCG test result > 5 IU/L ("positive")
- Has signed an informed consent form
- Affiliated with a health insurance plan
Exclusion criteria
- Patient deprived of liberty or under legal guardianship
- Patient refuses to participate in the study
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Screening
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07592806 · 2023_0004