- Trials with a EudraCT protocol (1,618)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (5)
1,618 result(s) found for: Pregnant women.
Displaying page 1 of 81.
EudraCT Number: 2009-016877-14 | Sponsor Protocol Number: H1N1-2009 | Start Date*: 2009-11-04 |
Sponsor Name:COPSAC | ||
Full Title: H1N1v Vaccination of Pregnant Women: A Longitudinal Cohort Study Characterizing Influenza A-H1N1v Vaccination in Pregnant Women | ||
Medical condition: Protection against Influenza A H1N1v disease | ||
Disease: | ||
Population Age: In utero, Preterm newborn infants, Newborns, Infants and toddlers, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000247-58 | Sponsor Protocol Number: PKZW-NZW201301 | Start Date*: 2013-09-30 |
Sponsor Name:KU Leuven Departement Ontwikkeling en Regeneratie | ||
Full Title: Pharmacokinetics of drugs used by pregnant women (paracetamol/macrolide antibiotics): in vivo pharmacokinetic study of pregnant versus non-pregnant women. | ||
Medical condition: 1) Pregnant women who, due to medical indication, need to take one of the experimental drugs (paracetamol, azithromycin or erythromycin) in the second or third trimester of there pregnancy 2) The s... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-002327-38 | Sponsor Protocol Number: NL77670.029.21 | Start Date*: 2021-05-26 | ||||||||||||||||
Sponsor Name:Academic Medical Center | ||||||||||||||||||
Full Title: PREGCOVAC-19: the follow up of pregnant women who received COVID-19 vaccination in the Dutch national vaccination program | ||||||||||||||||||
Medical condition: Pregnant women aged ≥ 18 years who are scheduled for COVID-19 vaccination within the Dutch national vaccination program with any of the currently or future available vaccines that are used for preg... | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002061-29 | Sponsor Protocol Number: 08227 | Start Date*: 2016-03-21 | |||||||||||
Sponsor Name:Consorci Sanitari de Terrassa | |||||||||||||
Full Title: Prospective randomized clinical trial comparing the effect of vaginal misoprostol synchronously with supracervical ball, versus only vaginal misoprostol for induction of labor. | |||||||||||||
Medical condition: Pegnant women with a term singleton pregnancy, cephalic presentation, reassuring fetal heart rate pattern, intact membranes and an unfavorable cervix (Bishop score less than 6), admitted to our ins... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002047-15 | Sponsor Protocol Number: CCSJ148X2202 | Start Date*: 2018-08-01 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A multicenter, randomized, patient, investigator and sponsor blinded, placebo-controlled phase II study to evaluate the efficacy and safety of CSJ148 in pregnant women with primary HCMV infection | |||||||||||||
Medical condition: Congenital human cytomegalovirus (HCMV) infection in pregnant women | |||||||||||||
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Population Age: In utero, Newborns, Infants and toddlers, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000145-40 | Sponsor Protocol Number: versión2.febrero2017 | Start Date*: 2017-09-20 |
Sponsor Name:montserrat zamora brito | ||
Full Title: Use of acupuncture for the reduction of hospital admissions in the induction of labor due to chronologically prolonged gestation. ACUPUNT STUDY | ||
Medical condition: This Clinical Trial will evaluate the efficacy and safety of acupuncture to promote labor in pregnant women who need an induction at birth and thus be able to give answers to all these women who a... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-000440-22 | Sponsor Protocol Number: Version17032021 | Start Date*: 2021-03-25 |
Sponsor Name:Universiteit Antwerpen | ||
Full Title: Vaccination against COVID-19 in Pregnant and Lactating Women in Belgium | ||
Medical condition: Vaccine responses to COVID19 vaccines administered in pregnant and lactating women | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-006560-11 | Sponsor Protocol Number: FARM7J4HCH | Start Date*: 2009-02-24 |
Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | ||
Full Title: Prevention of human cytomegalovirus (HCMV) mother-to-fetus transmission by administration of virus-specific hyperimmune globulin to pregnant women with primary HCMV infection | ||
Medical condition: Pregnant women with primary HCMV infection. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-000994-35 | Sponsor Protocol Number: 06032017 | Start Date*: 2018-08-02 | |||||||||||
Sponsor Name:Hospital General Universitario de Alicante | |||||||||||||
Full Title: Study of tolerability of iron liposome compared to ferrous sulphate in pregnant women with iron deficiency anemia. | |||||||||||||
Medical condition: Iron deficiency anaemia | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006080-23 | Sponsor Protocol Number: DPMFM PC1036 | Start Date*: 2007-03-21 |
Sponsor Name:Institute of Obstetrics and Gynaecology Trust | ||
Full Title: Vitamin D status in pregnancy and the effects of vitamin D supplementation in ethnic minority groups | ||
Medical condition: Low vitamin D levels in pregnant women especially in ethnic minority groups | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000446-30 | Sponsor Protocol Number: 02-2014 | Start Date*: 2014-07-23 |
Sponsor Name:Maasstad Ziekenhuis | ||
Full Title: Metformin vs Control to prevent gestational diabetes mellitus (GDM) in women with a high risk for GDM, an open label randomized controlled trial. The Medico-GDM trial. | ||
Medical condition: Pregnant women with a high risk of gestational diabetes mellitus (GDM) | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2010-020840-36 | Sponsor Protocol Number: V98_04 | Start Date*: 2011-08-08 | |||||||||||
Sponsor Name:Novartis Vaccines and Diagnostics GmbH | |||||||||||||
Full Title: A Phase II Randomized, Observer-Blind, Multi-Center, Controlled Study of a Trivalent group B Streptococcus Vaccine in Healthy Pregnant Women | |||||||||||||
Medical condition: Invasive group B streptococcus disease | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004763-40 | Sponsor Protocol Number: GQM14 | Start Date*: 2017-04-05 |
Sponsor Name:Sanofi Pasteur | ||
Full Title: Immunogenicity and Safety of Quadrivalent Influenza Vaccine (VaxigripTetra™) in Pregnant Women | ||
Medical condition: Prophylaxix of influenza in Pregnant Women | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-005792-25 | Sponsor Protocol Number: R04341 | Start Date*: 2017-12-22 | ||||||||||||||||||||||||||
Sponsor Name:Manchester University NHS Foundation Trust | ||||||||||||||||||||||||||||
Full Title: Feasibility study on the effects of L-citrulline on uteroplacental and cardiovascular function in hypertensive pregnant women | ||||||||||||||||||||||||||||
Medical condition: The medical condition that is to be investigated in this study is essential hypertension in pregnant women. In this study it is defined as diastolic BP of ≥90 mmHg (average of two clinic readings) ... | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-002697-80 | Sponsor Protocol Number: MADI-02 | Start Date*: Information not available in EudraCT |
Sponsor Name:Université Libre de Bruxelles | ||
Full Title: Maternal determinants of infant immunity to pertussis | ||
Medical condition: Vaccination against whooping cough in non-pregnant women and in pregnant women. Vaccination against whooping cough in the Belgian vaccination program in children from 2 months of age | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Under 18, Adults | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005198-30 | Sponsor Protocol Number: BBHV.02-2012 | Start Date*: 2013-04-30 |
Sponsor Name:LAURA TARRATS VELASCO | ||
Full Title: EFFICACY OF ADMINISTRATION OF HYOSCINE BUTILBROMIDE (BUSCOPAN®) ON PREGNANT WOMEN IN FIRST STAGE OF LABOUR IN CASE OF CERVIX RIGIDITY. (BBH V.04-2013 EUDRACT: 2012-005198-30) | ||
Medical condition: in case of cervix rigidity determination in first stage of labour, pregnant women will be offered to participate and if they accept they´ll be randomised to test or control group. Placebo or treat... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-017134-47 | Sponsor Protocol Number: EMPOWaR | Start Date*: 2010-03-04 | ||||||||||||||||
Sponsor Name:University of Edinburgh [...] | ||||||||||||||||||
Full Title: Efficacy of Metformin in Pregnant Obese Women, a Randomised Controlled Trial. | ||||||||||||||||||
Medical condition: Obesity in pregnancy | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-001587-29 | Sponsor Protocol Number: 02/04/2020-001 | Start Date*: 2020-04-08 | |||||||||||
Sponsor Name:Barcelona Institute for Global Health (ISGlobal) | |||||||||||||
Full Title: Hydroxychloroquine efficacy in preventing SARS-CoV-2 infection and CoVid-19 disease severity during pregnancy | |||||||||||||
Medical condition: SARS-SoV-2 infection and CoVid-19 disease | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004224-10 | Sponsor Protocol Number: N/A | Start Date*: 2013-12-06 |
Sponsor Name:Region Skåne | ||
Full Title: Prospective randomized trial comparing the effects of oxytocin and carbetocin on circulation and vascular tone at cesarean section | ||
Medical condition: Cesarean section of pregnant women | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002534-35 | Sponsor Protocol Number: 15022288 | Start Date*: 2005-09-14 |
Sponsor Name:Coombe Women's Hospital | ||
Full Title: Determination of plasma concentration of levobupivicaine following low concentration epidural infusion of levobupivicaine in pre-eclamptic and non pre-eclamptic nulliparous women. | ||
Medical condition: This clinical trial is an non-interventional observational clinical study, measuring the plasma levels of the levobupivicaine during labour with an epidural infusion. We will measure levels in pre-... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
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