Miscarriage

12

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

Condition / disease
Location
Status: Recruiting

Is Decreased Ovarian Reserve Related to an Increased Number of Previous Early Miscarriages?

This study aims to explore the potential correlation between decreased ovarian reserve and previous history of early miscarriage.

Participants needed: 2,059
Trial details
Biological sex: FemaleType: ObservationalSponsor: ART Fertility Clinics LLCUpdated: Jun 25, 2026Locations: 3
Eligibility criteria

Severe male factor (azoospermia, cryptozoospermia, severe oligoasthenoteratozoos... [+6]

Status: Recruiting

Hysteroscopy vs. Endouterine Aspiration in the Management of Trophoblastic Retention

Introduction: Incomplete early miscarriage is defined as early miscarriage with persistent intrauterine material on ultrasound. Intrauterine retention of trophoblastic debris is not an uncommon phenomenon. These retentions may initially be asymptomatic but are often responsible for persistent metrorrhagia and endometritis. This symptomatology often accentuates the psychological distress of patients mourning the pregnancy. Incomplete miscarriages are mainly managed by the gynecological emergency department. The recommendations of the Collège National des Gynécologues et Obstétriciens Français (CNGOF) suggest as a first line of treatment: either surgical management or expectant care. The choice between the two is left to the discretion of the doctor and the patient. there are no clear recommendations as to the choice between hysteroscopy and aspiration. Within the teams, the choice is often made according to the habits and protocols of the service, according to the equipment available and the skills of the gynaecologists. Aim: The main objective is to compare the efficacy of management by endo-uterine aspiration vs. management by hysteroscopy of trophoblastic retention after early miscarriage, at 6 weeks after surgery, by endovaginal ultrasound. Methods: This is a prospective, multicenter, randomized, open-label, two-arms, parallel therapeutic clinical trial comparing hysteroscopy versus endouterine aspiration for the management of trophoblastic retention after spontaneous miscarriage. Patients will be randomized (110 per arm) after verification of eligibility criteria and signature of consent, on the day of the operation: * Arm A: 110 patients treated by operative hysteroscopy * Arm B: 110 patients treated by endo-uterine aspiration

Participants needed: 220
Trial details
Age: 18-42Biological sex: FemaleType: InterventionalSponsor: University Hospital, MontpellierUpdated: Jun 22, 2026Locations: 4
Eligibility criteria

Management for trophoblastic retention after early spontaneous miscarriage (<14... [+2]

Known uterine malformation [+8]

Status: Recruiting

PERIodontal Disease, Microbiota and Miscarriage

Cross-sectional non-interventional observational pilot study recruiting women whom had repeated miscarriages (= at least 3 miscarriages).The information will be collected during a routine maintenance, complete oral clinical and radiological examination (assessment carious, periodontal, mucosal and functional), which is part of the routine assessment in the service of odontology from Toulouse University Hospital. Saliva and subgingival plaque samples, classically carried out in routine dental surgery as part of the health check-up oral, will be used to carry out bacterial assays.

Participants needed: 30
Trial details
Age: Up to 18Biological sex: FemaleType: ObservationalSponsor: University Hospital, ToulouseUpdated: May 12, 2026Locations: 1
Eligibility criteria

women whom had repeated miscarriages [+1]

under antibiotic prebiotic or probiotics treatment one month prior to the study [+1]

Status: Not yet recruiting

Walk With Me (WWM) for Perinatal Grief

The goal of this clinical trial is to learn if the Along With Me web-based intervention works to decrease posttraumatic stress symptoms and suicidal ideation among bereaved parents following pregnancy and early infant loss. It will also learn whether peer guides provide additional improvements on these outcomes. The main questions it aims to answer are: • Do people who receive Along With Me or Along With Me plus a Peer Guide compared to services as usual have lower posttraumatic stress symptoms and suicidal ideation than those who do not receive the intervention? Researchers will compare Along With Me and Along With Me plus a Peer Guide to services as usual (referrals made in the hospital setting) to see if Along With Me works to prevent and address posttraumatic stress symptoms and suicidal ideation. Participants will: * Receive access to a mobile app with approximately 10 therapeutic modules about how to manage grief and other symptoms. * Receive check-ins with a Peer Guide (in the Peer Guide condition only)

Participants needed: 300
Trial details
Age: 15+Biological sex: AllType: InterventionalSponsor: Oregon Research Behavioral Intervention Strategies, Inc.Updated: Mar 6, 2026Locations: 1
Eligibility criteria

Within the first month of pregnancy or early infant loss [+3]

Not pregnant or has not experienced an early infant loss [+3]

Status: Recruiting

Cohort of Patients Presenting Unexplained Recurrent Miscarriages and Identification of Early Miscarriage Recidivism Factors

About 1 to 3% of women of childbearing age suffer repeated early spontaneous miscarriages (RCF) defined by at least 3 fetal losses before 14 weeks of gestation. RCFs may be linked to parental chromosomal abnormalities, congenital or acquired uterine abnormalities, hormonal causes (e.g. type 1 and 2 diabetes, ovarian failure), infectious etiology, constitutional or acquired thrombophilia or sickle cell disease. The presence of antiphospholipid antibodies, antithyroid and anti-transglutaminase antibodies in approximately 10% of cases suggests an autoimmune origin for these fetal losses. The role of other antibodies, in particular non-conventional antiphospholipid antibodies, remains to be established. Indeed half of RCF cases are thought to be due to an immunological dysregulation of the mother leading to a decrease in tolerance to the fetus. Several studies have shown immune abnormalities, such as an imbalance of pro and anti-inflammatory cytokines, an increase in cytotoxic cells and a defect in regulatory cells in the blood of patients. The assessment of these immune abnormalities is not currently performed routinely in France in women presenting with recurrent early miscarriages. When one of these known causes is excluded, it is unexplained RCF which represents 50% of RCF. Over half of these women with RCF may be linked to aneuploidies and primary spontaneous recurrent abortions. Assessing the degree of aneuploidy and the genetic origin of foetal losses remains difficult to date, as examination of the miscarriage product is rarely available, due to the spontaneous nature of the loss. An implantation failure (IF) is defined as the absence of pregnancy following the transfer of a good-quality embryo into the uterine cavity. These implantation failures can be due to embryonic factors, maternal factors, or caused by inappropriate stimulation and/or difficult transfers. In the literature, recurrent implantation failure (RIF) is defined as the absence of pregnancy after 3 attempts of transferring good-quality embryos, taking maternal age into account Setting up a prospective cohort of patients with RFC is an essential step in exploring the aetiological factors of RCF and in order to enable better treatment.

Participants needed: 700
Trial details
Age: 18-50Biological sex: FemaleType: ObservationalSponsor: Assistance Publique - Hôpitaux de ParisUpdated: Dec 19, 2025Locations: 1
Eligibility criteria

Age 18 to 50 years [+3]

patients who do not agree the use of their data [+2]

Status: Recruiting

Use of Aromatase Inhibitor Before Misoprostol in Medical Termination of Miscarriage

Abortion is one of the most common complications of pregnancy. Missed abortion is a type of abortions, occurs in 15%-20% of clinically diagnosed pregnancies and is defined as the retention of pregnancy products in the uterus for several days or weeks after death of the fetus.

Participants needed: 70
Trial details
Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Aswan UniversityUpdated: Aug 7, 2025Locations: 1
Eligibility criteria

Missed or anembryonic pregnancy. [+4]

Previous attempt to terminate the pregnancy. [+6]

Status: Recruiting

Letrozole and Misoprostol for Early Pregnancy Loss Management

A pilot cohort study to preliminarily investigate the efficacy of pretreatment with letrozole 10 mg daily for three consecutive days followed by treatment with misoprostol 800 mcg vaginally for medical management of early pregnancy loss in a US population. Patients will be followed to assess efficacy of this treatment regimen, as well as additional interventions needed, side effects, adverse events, and patient acceptability.

Participants needed: 30
Trial details
Phase: Phase 2Age: 18+Biological sex: FemaleType: InterventionalSponsor: University of PennsylvaniaUpdated: Aug 5, 2025Locations: 1
Eligibility criteria

Able to participate in the informed consent process and provide a signed and dat... [+5]

Incomplete or inevitable abortion [+3]

Status: Recruiting

The Heartland Study

The Heartland Study is a prospective, observational study that will enroll up to 2,600 pregnant participants across the Heartland States in the U.S.. The objective of the Heartland Study is to address major knowledge gaps concerning the health effects of herbicides on maternal and infant health. The study is being conducted to evaluate the associations between environmental exposures to herbicides during and after pregnancy and reproductive health outcomes. The study is measuring multiple biomarkers of herbicide exposure among pregnant Midwesterners and their partners to evaluate associations with pregnancy and childbirth outcomes, epigenetic biomarkers of exposure, and child development.

Participants needed: 2,600
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Heartland Health Research AllianceUpdated: Jun 29, 2025Locations: 4
Eligibility criteria

Pregnant persons ages 18 or older at time of consent who are ≤20+6 weeks pregnan... [+1]

Participants who are not fluent in and/or do not fully understand, read, write,... [+1]

Status: Recruiting

A Prospective Study Evaluating the Impact of Conservative Management on Retained Products of Conception and EMV

The goal of this observational study is to learn about the therapeutic effects of the conservative treatment approach on pepole with retained products of conception (RPOC) and Enhanced myometrial vascularity (EMV). The main question it aims to answer is: Is it possible to achieve the natural resolution of RPOC by combining it with EMV through conservative treatment? Participants will receive conservative treatment (such as mifepristone, GnRH-a, or expectant management) following the initial diagnosis of RPOC and EMV, and the therapeutic efficacy of the conservative approach will be assessed after the completion of two menstrual cycles.

Participants needed: 120
Trial details
Biological sex: FemaleType: ObservationalSponsor: Fu Xing Hospital, Capital Medical UniversityUpdated: Jun 15, 2025Locations: 1
Eligibility criteria

Recent history of miscarriage or delivery (within the past 8 weeks) [+3]

Heavy vaginal bleeding (requiring immediate surgical intervention) [+6]

Status: Recruiting

Exploration of Allograft Humoral Rejection in Chronic Histiocytic Intervillositis

Chronic histiocytic intervillositis (CHI) is a rare condition with an incidence of 5 in 10,000 pregnancies. This rare condition is associated with placental inflammatory lesions leading to severe and recurrent obstetrical complications: intrauterine growth retardation (IUGR), fetal death in utero and miscarriage. The pathophysiological mechanisms of CHI are poorly understood, while the empirical treatments prescribed to prevent recurrence are cumbersome and of poor efficacy. Recent findings suggest that an alloimmune response may play a role. In a recent work, the investigators have demonstrated the role of maternal alloantibodies directed against fetal HLA antigens in two patients followed for recurrent IUGR associated with CHI. Their work suggests that a humoral alloimmune response directed against fetal HLA antigens mimics an allograft rejection process. The investigators propose to extend the preliminary results obtained in these patients to provide new insights into the pathophysiological mechanisms of CHI, and eventually to predict the risks of fetal loss.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Assistance Publique - Hôpitaux de ParisUpdated: Nov 6, 2024Locations: 1
Eligibility criteria

Mother and father ≥ 18 years old [+9]

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]

Status: Not yet recruiting

Interest of a Short Early Psychological Care in Women With Miscarriage

Miscarriage is a very common complication of pregnancy, accounting for 15.3% (95% CI 12.5-18.7%) of diagnosed pregnancies. Miscarriage would affect one in ten women during her lifetime. Worldwide, 23 million miscarriages occur annually. Because of its frequency, miscarriage isoften considered as trivial event by caregivers. Still, miscarriage can be a traumatic event. Literature is consistent on the psychological morbidity associated with miscarriage. Anxiety, depression, post-traumatic stress have been studied in women after miscarriage. Cohort studies and clinical trials suggest that psychological and supportive interventions performed in women after miscarriage may improve women's psychological well-being and reduce miscarriage complications in subsequent pregnancies. However, to date, the literature is considered insufficient on the psychological care of women after a miscarriage.

Participants needed: 932
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Université de Reims Champagne-ArdenneUpdated: May 15, 2023
Eligibility criteria

women with an early miscarriage (defined by a spontaneous termination of pregnan... [+2]

ectopic pregnancy [+3]