Prednisolone Administration in Patients With Unexplained REcurrent MIscarriages

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexFemale
Age18-40
SponsorLeiden University Medical Center

About this trial

Recurrent miscarriages (RM) affects 3% of all fertile couples, but remains unexplained in most cases, limiting therapeutic options. Possibly the maternal immune system plays a role in recurrent miscarriage. Prednisolone suppresses the immune system and might enable development of normal pregnancy.

In this randomized controlled clinical trial the investigators will study the effect of prednisolone on the live birth rate in patients with RM. Secondary, the tolerability and safety for mother and child and the cost-effectiveness is investigated.

In the study one group of pregnant women with RM and gestational age \<7 weeks will receive prednisolone, the other group will receive a placebo. Total use of the medicine during this study is 8 weeks, further care during the study is routinely antenatal care. Subjects will be asked to fill in 4 short questionnaires and will have contact with a research nurse at different time points to gain information on the course of the pregnancy and possible side effects.

Results of the study will be implemented in (inter) national guidelines, to effect everyday practice.

Eligibility criteria

Qualifiers

Unexplained recurrent pregnancy loss: defined as the loss of ≥2 pregnancies, without any known cause for RM (parental chromosomal abnormalities, uterine anomalies, acquired or hereditary thrombophilia, endocrine diseases (such as hypothyroidism or diabetes)).

all consecutive or non-consecutive pregnancy losses before the 24th week of gestation verified by ultrasonography or uterine curettage and histology

non-visualized pregnancies (including biochemical pregnancy losses and/or resolved and treated pregnancies of unknown location), verified by positive urine or serum hCG Ectopic and molar pregnancies are not included

Age 18 - 39 years at randomization (likelihood of miscarriages due to chromosomal aberrations is higher when age > 39 years. Such miscarriages are unlikely to be pre-vented by prednisolone therapy)

Disqualifiers

Any of the following diagnosis for the recurrent miscarriages

Antiphospholipid syndrome (lupus anticoagulant and/ or anticardiolipin anti-bodies and/or beta-2 glycoprotein [IgG or IgM)

Congenital uterine abnormalities (as assessed by 2D or 3d ultrasound, hys-terosonography, hysterosalpingogram or hysteroscopy)

Abnormal parental karyotype

Trial design

Treatments tested in this trial

  • Prednisolone
  • Placebo

Treatment groups

490 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Leiden University Medical Center

Lead sponsor

Amsterdam University Medical Center

Collaborator

Erasmus Medical Center

Collaborator

Academisch Ziekenhuis Groningen

Collaborator

Maastricht University Medical Center

Collaborator

Isala

Collaborator

Catharina Ziekenhuis Eindhoven

Collaborator

Haaglanden Medical Centre

Collaborator

Amphia Hospital

Collaborator

Radboud University Medical Center

Collaborator

Jeroen Bosch Ziekenhuis

Collaborator

Onze Lieve Vrouwe Gasthuis

Collaborator