Search Medical Condition
Please enter condition
Please choose location from dropdown
Clear Trial Filters

Pregnancy Complications Clinical Trials

A listing of Pregnancy Complications medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.

RESULTS

Found (67) clinical trials

The purpose of this research study is to see if it is beneficial to treat high blood pressure during and after pregnancy NYU Winthrop Hospital Clinical Trials Center is seeking pregnant participants, who are 18 years old or older and who have been diagnosed with high blood pressure to participate ...

Phase N/A

Maternal Cancer Diagnosis and Treatment During Pregnancy:a Database for Maternal Fetal and Neonatal Outcomes

Approximately 1:1000 pregnancies are complicated by cancer. Breast cancer is the most common type diagnosed during pregnancy. Termination of pregnancy has not demonstrated an improvement in survival. Results of an international collaborative study reported similar overall survival for patients diagnosed with breast cancer in pregnancy compared to nonpregnant patients. The ...

Phase N/A

Impedance Cardiography to Decrease the Risk of Preeclampsia

Impedance cardiography helps determine whether vasoconstriction or an elevated cardiac output is occurring. The test is easy to perform and non invasive. The treatment for an elevated cardiac output in pregnancy is a beta-blocker while a vasodilator is used for vasoconstriction. If a beta-blocker is given to someone that vasoconstricted, ...

Phase N/A

Pregnancies Complicated by Fetal Anomalies

Repository data will be collected from the medical record and entered into the data base after the patient has completed the appointment. Data collection will continue into the postpartum period for each participant. Data collection will continue for the child during the treatment of the medical condition, up to approximately ...

Phase N/A

Study on Antithrombotic Prevention in Thrombophilia and Pregnancy Loss

The occurrence of a spontaneous fetal loss (FL) is a rather frequent event: it has been estimated that up to 15% of pregnancies result in a fetal loss. However, recurrent events, defined as >2 or >3 loss, depending on the guidelines used (American College of Obstetricians and Gynecologists or Royal ...

Phase N/A

A clinical research study for the treatment of Hepatitis C virus, CONGENITAL ANOMALY NOS, Pregnancy Complications, Atresia, Hepatitis C

Ribavirin, a nucleoside analog with antiviral activity, is used in combination with interferons or pegylated interferons for the treatment of chronic hepatitis C (HCV). Extensive clinical studies have demonstrated that combination therapy with ribavirin and interferons or pegylated interferons are efficacious treatments for HCV. However, ribavirin has been assigned a ...

Phase N/A

Pregnancy Complications - A Probiotic Interventional Study

The main of the Project is to determine if dietary supplementation intake of probiotics are associated with a decreased risk of spontaneous preterm delivery and preeclampsia in a randomized Clinical trial. Investigators also want to further investigate the relationship between intake of probiotics and the degree of inflammation in different ...

Phase N/A

National Study on Listeriosis and Listeria

Context: Listeriosis is a foodborne infection responsible for severe disease. Surveillance of human listeriosis in France is based on both mandatory reporting of cases and voluntary submission of L. monocytogenes strains to the National Reference Center for Listeria (NRC) since 1999. The exhaustiveness of this reporting estimated by capture-recapture is ...

Phase N/A

Physical Activity and Gestational Complications

The association between physical activity and several complication of pregnancy will be evaluated. Patients with complications of pregnancy will be recruited. Physical activity will be evaluated using questioner or smart bracelet.

Phase N/A

Negative Pressure Wound Therapy to Prevent Wound Complications Following Cesarean Section in High Risk Patients

Once consent has been obtained from patients, an envelope containing the study allocation will be retrieved from the Pyxis. Non-wound vac patients will undergo wound closure with subcutaneous fat closure with Vicryl in all cases that this is practicable (in extremely thin patients, this may not be possible), followed by ...

Phase N/A