Habitual Abortion

2

Review clinical trials related to Habitual Abortion. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Association Between Plasma Level of Mannose Binding Lectin and Human Reproduction

A low plasma level of mannose binding lectin (p-MBL) is associated with unexplained recurrent pregnancy loss (RPL), but it is not investigated if it is associated with unexplained reproductive failure in general, including recurrent implantation failure (RIF) after assisted reproductive technology (ART) (including IVF, ICSI and FET), recurrent pregnancy loss (RPL) after spontaneous conception, and RPL after ART.

Participants needed: 500
Trial details
Age: 18-41Biological sex: FemaleType: ObservationalSponsor: Aalborg University HospitalUpdated: Nov 24, 2025Locations: 1
Eligibility criteria

3 consecutive pregnancy losses after spontaneous conception [+2]

Age <18 or >45 years [+5]

Status: Recruiting

Prednisolone Administration in Patients With Unexplained REcurrent MIscarriages

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.

Participants needed: 490
Trial details
Phase: Phase 4Age: 18-40Biological sex: FemaleType: InterventionalSponsor: Leiden University Medical CenterUpdated: May 24, 2024Locations: 1
Eligibility criteria

Unexplained recurrent pregnancy loss: defined as the loss of ≥2 pregnancies, wit... [+5]

Any of the following diagnosis for the recurrent miscarriages [+19]