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Pregnancy clinical trials

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NCT ID: NCT03997045 Recruiting - Healthy Clinical Trials

Exercise During Pregnancy and Urinary Incontinence

Start date: March 1, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to examine the effect of a supervised physical exercise program during pregnancy on urinary incontinence.

NCT ID: NCT03993015 Completed - Clinical trials for Pregnant Women Less Than 14 Weeks of Gestation

Accuracy of eDiagEPU, a Medical Computerized Tool for EPU

eDiagEPU
Start date: July 1, 2019
Phase:
Study type: Observational

In a recently published study, a poor knowledge of guidelines in the field of early pregnancy was observed in France, Belgium and Switzerland. To improve the respect of the most recent criteria of diagnoses, a computerized tool was developped.

NCT ID: NCT03984630 Completed - Pregnancy Clinical Trials

Pregnancy Intervention Revolving Around Goal-focused Education (GIRAFE)

GIRAFE
Start date: August 11, 2016
Phase: N/A
Study type: Interventional

The purpose of study is to learn if consuming ≥30 grams or more of fiber per day can help pregnant women gain an appropriate amount of weight during their pregnancy.

NCT ID: NCT03982732 Recruiting - Pregnancy Clinical Trials

Maternal Antibody in Milk After Vaccination

MAMA
Start date: August 7, 2018
Phase:
Study type: Observational

Single-centre observational pilot study exploring pertussis specific antibody concentration in the breastmilk of women vaccinated against pertussis in pregnancy at different gestational ages. This study is made up of two stages: first stage to confirm recruitment methods and optimise the laboratory assay and a second stage to complete recruitment for the pilot study.

NCT ID: NCT03961178 Recruiting - Pregnancy Clinical Trials

A Cohort Study for the Following up of Conization

Start date: June 3, 2019
Phase:
Study type: Observational

This study is to investigate the oncologic and obstetric outcomes in patients with conization for uterine cervical lesions from January 1, 2000 to January 1, 2019 in Peking Union Medical College Hospital. The primary objectives consist of following: 1. The cumulative incidences of precancerous lesions and cancers of lower genital tract in patients who accepted conization for high grade intraepithelial neoplasia (HSIL), carcinoma in situ and stage IA1 cancer (FIGO 2009) 2. The cumulative pregnancy rates in patients sparing the fertility The secondary objectives consist of following: 1. The effects of surgical protocols (modified Sturmdorf method and "8" figure suture) and energy equipment (cold knife and monopolar electrical cautery) on the oncologic and obstetric outcomes, and on the histological components. 2. A full description of histological components of the conization specimens 3. The cytological and virus outcomes after conization, based on the thin prep liquid-based cytology test (TCT) and high-risk human papillomavirus (HPV) testing

NCT ID: NCT03944317 Not yet recruiting - Pregnancy Clinical Trials

Azithromycin (AZ) and Sulphadoxine-pyrimethamine (SP) for Malaria Prevention in Pregnant Women (IPT-AZ/IPT-SP)

Start date: June 1, 2019
Phase: N/A
Study type: Interventional

AZITHROMYCIN VERSUS SULPHADOXINE‑PYRIMETHAMINE FOR PROPHYLAXIS AGAINST MALARIA IN PREGNANCY IN OWO, SOUIHWESTERN NIGERIA: A RANDOMISED CONTROLLED TRIAL OBJECTIVE: This study is to compare the efficacy of Azithromycin versus sulphadoxine‑pyrimethamine as options of chemoprophylaxis against malaria in pregnancy. METHOD: This is a randomized controlled trial with parallel assignment that will be conducted in the Obstetrics and Gynaecology department of the Federal Medical Centre. One hundred and sixty four (164) pregnant women who are eligible will be randomly allocated to 2 groups (A and B) of 84 each, using computer generated random numbers. Group A will receive sulfadoxine-pyrimethamine for malaria prophylaxis while Group B will receive azithromycin. All other aspects of antenatal care till delivery will be the same for all the women recruited. Maternal venous blood samples for malaria parasitaemia will be collected on recruitment and repeated at follow-up visits at any gestation there are symptoms of malaria; maternal peripheral blood film, placental and cord blood samples will be collected at delivery. All data will be documented in the data collection sheet. The results obtained will be subjected to statistical analysis using statistical package for social sciences (SPSS) version 21, Armonk, NY:IBM. The level of significance will be set at 5%. Outcomes will be compared across groups using Chi-square.

NCT ID: NCT03942536 Completed - Pregnancy Clinical Trials

The MOMENTUM Study (Monitoring Maternal Emergency Navigation and Triage on Mfangano

MOMENTUM
Start date: May 15, 2019
Phase:
Study type: Observational

This is an observational cohort study that will assess barriers influencing access to emergency pregnancy, obstetrical and neonatal care.

NCT ID: NCT03941041 Recruiting - Pregnancy Clinical Trials

Impact of Prenatal Yoga Practice on Birth Outcome

Start date: May 15, 2019
Phase: N/A
Study type: Interventional

Yoga is a body-mind practice that encompasses a system of postures (asana), stretching exercises combined with breathing (pranayama) and meditation (dharana). About 70% of practitioners are women, the majority of them in their reproductive age. Yoga is on the rise among pregnant women. Prenatal yoga appears to help pregnant women develop mental and physical health and build a connection with their unborn baby. It reduces stress and anxiety, lower back pain, carpal tunnel syndrome symptoms, nausea, headaches and shortness of breath, improves sleep and increase strength, flexibility and endurance of muscles needed for childbirth. A limited number of prospective randomized trials exist about the benefits of yoga in pregnancy and childbirth. An analysis of how yoga exercises in pregnancy affect the labour pattern, the outcome as well as the caesarean rate in a population of European pregnant women will be performed.

NCT ID: NCT03932851 Recruiting - Pregnancy Clinical Trials

Clinical Study on the Effect of IVF-ET on Mother-to-child Transmission of Hepatitis B Virus

Start date: August 1, 2018
Phase:
Study type: Observational

This study is intended to retrospectively collect HBV-infected pregnant women and non-HBV-infected pregnant women who have been born in IVF in the investigators' hospital, collect pregnant women's data during pregnancy, newborn birth data, and hepatitis B virus in July after birth of newborns born to HBV-infected pregnant women. Infection, explore the impact of HBV infection on IVF outcomes and whether IVF operations increase the risk of mother-to-child transmission of HBV.

NCT ID: NCT03931460 Completed - Pregnancy Clinical Trials

Feasibility of Medical Abortion by Telemedicine in Mexico

Start date: April 1, 2019
Phase:
Study type: Observational

This study is designed to obtain preliminary data on the safety, acceptability, and feasibility of direct-to-consumer telemedicine abortion in Mexico.