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Pregnancy clinical trials

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NCT ID: NCT02270801 Recruiting - Pregnancy Clinical Trials

Recombinant Human Thrombopoietin (rhTPO) in Management of Immune Thrombocytopenia (ITP) in Pregnancy

Start date: October 2014
Phase: Phase 3
Study type: Interventional

This clinical trial is undertaking by Qilu Hospital of Shandong University, aims at evaluating efficacy and safety of rhTPO in management of ITP in pregnancy.

NCT ID: NCT02247297 Recruiting - Pregnancy Clinical Trials

Pancreatic Stone Protein (PSP) in Pregnant Women

Start date: September 2014
Phase:
Study type: Observational

This prospective, single centred cohort study evaluates the physiological course of the potentially novel biomarker PSP in pregnant women as well as its predictive role in the development of inflammatory complications during pregnancy.

NCT ID: NCT02240927 Recruiting - Pregnancy Clinical Trials

Anticoagulation Regimens in Pregnant Patients With Prosthetic Heart Valves

Start date: January 2010
Phase: N/A
Study type: Interventional

Pregnancy is associated with increased risk of thrombosis among women with mechanical prosthetic heart valves.However, the best anticoagulant treatment strategies for pregnant patients with prosthetic heart valves have been controversial. In this study the investigators wanted to identify the most effective and safe regimen among different anticoagulant regimens.

NCT ID: NCT02210598 Recruiting - Pregnancy Clinical Trials

Outpatient Labor Induction With the Transcervical Foley Balloon

Start date: March 2014
Phase: N/A
Study type: Interventional

This study represents the first randomized trial comparing traditional inpatient induction with a transcervical foley catheter versus outpatient induction with immediate removal of a transcervical foley catheter. The immediate removal technique allows the induction process to begin in the hospital setting, but allows the patient to go home without a foreign body in situ. The investigators hypothesize the outpatient group will spend less time hospitalized prior to discharge. Additionally, the investigators will explore the vaginal delivery rates and maternal/neonatal safety profiles between groups.

NCT ID: NCT02192177 Recruiting - Pregnancy Clinical Trials

Apoptosis May Have a Role in Etiopathogenesis of Obstetric Cholestasis.

Start date: September 2013
Phase: N/A
Study type: Observational

Intrahepatic cholestasis of pregnancy is a disease specific to pregnancy period; especially late second and third trimester. We aimed to investigate the role of apoptosis in etiopathogenesis of obstetric cholestasis.

NCT ID: NCT02158429 Recruiting - Pregnancy Clinical Trials

Study of Ultrasound To Increase Parental Bonding in Women With Substance Use Disorders

Start date: April 2011
Phase: N/A
Study type: Interventional

1. A randomized trial of 3-dimensional vs. 2-dimensional ultrasound, comparing scores on the Maternal Antenatal Attachment Scale (MAAS), a validated instrument measuring maternal attachment as a marker of maternal bonding. The hypothesis is that 3-dimensional ultrasound is better at eliciting maternal attachment than 2-D 2. To assess changes in maternal confidence to stop using drugs and quit/reduce smoking with 3-D vs. 2-D ultrasound. Again, the hypothesis is that 3-D ultrasound will improve the woman's confidence to stop using substances. 3. To evaluate if 3-D ultrasound improves paternal attachment as measured by pre- and post- scores on the Paternal Antenatal Attachment Scale (PAAS). The hypothesis is that 3-D ultrasound will have a greater effect on PAAS scores than 2-D.

NCT ID: NCT02155751 Recruiting - Obesity Clinical Trials

Bringing NELIP for Obese Pregnant Women Into Clinical Practice

Start date: July 2012
Phase: N/A
Study type: Interventional

This is a pilot project in which investigators will recruit obese (pre-pregnancy BMI of ≥ 35 kg/m2) women from the newly developed "My Clinic" at London Health Sciences Centre as well as normal obstetrical care at London Health Sciences Centre. Patients will be randomized to one of three treatment groups: 1) the full Nutrition and Exercise Lifestyle Intervention Program (NELIP), 2) Nutrition program only, or 3) Exercise program only. The investigators hypothesize that the evidence-based NELIP for obese pregnant women will be feasible to adopt in a clinical setting and will prevent excessive gestational weight gain, gestational diabetes and promote healthy infant growth patterns at the 6 and 12 month milestones. Outcomes may be improved in My Clinic over normal obstetrical care patients with interprofessional services.

NCT ID: NCT02129465 Recruiting - Pregnancy Clinical Trials

Immunological Characteristics of Maternal-fetal Transmission of Cytomegalovirus in Pregnancy

CMV
Start date: June 2014
Phase: N/A
Study type: Observational

Analysis of several characteristics of blood from pregnant women with CMV infection according to maternal-fetal transmission. These include CMV viral load, cytokine profile in response to in-vitro stimulation with CMV peptides, meticulous analysis of anti CMV antibodies, maternal DNA polymorphism and microarray of gene expression.

NCT ID: NCT02116842 Recruiting - Pregnancy Clinical Trials

Minimum Effective Dose (MED) & Epidural Bupivacaine

Start date: December 2012
Phase: Phase 4
Study type: Interventional

Local anaesthetics are highly toxic drugs. They can cause toxicity by an absolute overdose, accidental injection in a blood vessel or slow absorption from the area of injection. The risk of toxicity when performing regional anaesthesia can be reduced significantly by injecting the optimal dose of local anaesthetic at the correct site. To date most of the local anaesthetic dose finding studies for epidural labour analgesia has focused on ED50 ( the dose effective in 50% of patients). The purpose of this research study is to find out the ED95 dose (the dose effective in 95% of patients) of local anaesthetic for epidural analgesia in labour. The dose determined from this research trial will guide the anaesthetists to the optimal starting dose of the local anaesthetics for epidural analgesia in labour. This would lead to decreased chances of toxicity and will improve patient safety. We aim to recruit a total of 100 pregnant patients in early labour (cervical dilatation ≤ 5 cm) requesting epidural analgesia to answer the research question based on the continual reassessment method. Patients will be recruited according to well-defined criteria. They will be fully informed about the study and have the choice of not participating or opting out at any time during the study. It is not going to affect the kind of treatment they receive. The experts in the field with full safety precautions will perform this study at St James' Hospitals, Leeds.

NCT ID: NCT02109588 Recruiting - Pregnancy Clinical Trials

Early Prevention of Childhood Obesity: an Active Pregnancy

Start date: March 2014
Phase: N/A
Study type: Interventional

The main aim of this study was to examine the effect of a supervised physical exercise program on the prevention of childhood obesity and its impact on the motor development of the offspring.