- Trials with a EudraCT protocol (59)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
59 result(s) found for: Childbirth.
Displaying page 1 of 3.
EudraCT Number: 2012-000356-33 | Sponsor Protocol Number: oxy123 | Start Date*: 2013-03-27 | |||||||||||
Sponsor Name:Västra Götaland | |||||||||||||
Full Title: Delay in labour due to ineffective uterine contractions is still a major problem in modern obstetric care. It is one of the main reasons for the increased rate of operative deliveries, particularly... | |||||||||||||
Medical condition: Labor dystocia (LD) also referred to as prolonged labour is a commonly identified problem in modern delivery care with three described possible causes: inefficient uterine action, occiputposterior ... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002978-39 | Sponsor Protocol Number: Ambulante_Geburtseinleitung | Start Date*: 2019-04-25 | |||||||||||
Sponsor Name:Medizinische Universität Graz | |||||||||||||
Full Title: Women's satisfaction with outpatient double-balloon catheter versus inpatient dinoprostone vaginal insert for induction of labour | |||||||||||||
Medical condition: Induction of labour | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: AT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005257-22 | Sponsor Protocol Number: RG_12-151 | Start Date*: 2013-07-12 |
Sponsor Name:University of Birmingham | ||
Full Title: Remifentanil intravenous patient controlled analgesia (PCA) versus intramuscular pethidine for pain relief in labour: a randomised controlled trial | ||
Medical condition: Childbirth | ||
Disease: | ||
Population Age: | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-002031-32 | Sponsor Protocol Number: PASS-2007 | Start Date*: 2008-05-05 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA S. GERARDO DI MONZA | |||||||||||||
Full Title: Phase III study protocol to compare conservative and active treatment during the third stage of labour in physiological childbirth | |||||||||||||
Medical condition: THIRD STAGE OF LABOR MANAGEMENT | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000823-15 | Sponsor Protocol Number: DIASA3 | Start Date*: 2019-10-18 | |||||||||||
Sponsor Name:Oslo University Hospital | |||||||||||||
Full Title: Glucose metabolism in South Asian women with impaired glucose tolerance or impaired fasting glucose. DIAbetes in South Asians – DIASA 3 A 12-week intervention trial with oral antidiabetic medicati... | |||||||||||||
Medical condition: Pre-diabetes in women of South Asian ethnicity. Women of South Asian ethnicity with previous gestational diabetes, where pre-diabetes in the form of impaired glucose tolerance or impaired fasting ... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NO (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003319-76 | Sponsor Protocol Number: MVDV/ER082019 | Start Date*: 2019-10-09 |
Sponsor Name:Univerity Hospitals Leuven | ||
Full Title: High volume PCEA versus PIEB for labor analgesia: a randomized, double-blind multicenter non-inferiority study in nulliparous women. | ||
Medical condition: providing adequate analgesia during child birth | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001829-11 | Sponsor Protocol Number: UoL001337 | Start Date*: 2018-10-04 | |||||||||||
Sponsor Name:University of Liverpool | |||||||||||||
Full Title: The Carboprost or Oxytocin Postpartum haemorrhage Effectiveness Study. Carboprost vs Oxytocin as the First Line Treatment of Primary Postpartum Haemorrhage; A phase IV, double-blind, double-dummy, ... | |||||||||||||
Medical condition: Primary postpartum haemorrhage | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004343-12 | Sponsor Protocol Number: ICARISTrialProtocol | Start Date*: 2015-10-07 |
Sponsor Name:Mater Research Institute University of Queensland | ||
Full Title: Impact on Caesarean Section Rates Following Injections of Sterile Water | ||
Medical condition: Back pain in labour and childbirth | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003577-24 | Sponsor Protocol Number: 1018 | Start Date*: 2004-12-10 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: remifentanil in continuos infusion as a labour analgesic | |||||||||||||
Medical condition: analgesia in partum | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001945-29 | Sponsor Protocol Number: 20170504 | Start Date*: 2017-09-20 | ||||||||||||||||
Sponsor Name:Linköping University, Department of clical and Experimental Medicine | ||||||||||||||||||
Full Title: Immediate post partum LNG-IUS insertion or standard insertion procedure after childbirth An open-label, randomized, multicenter study | ||||||||||||||||||
Medical condition: Contraception | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: SE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-002035-30 | Sponsor Protocol Number: TOFACOV-2 | Start Date*: 2020-05-15 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA OSPEDALI RIUNITI DI ANCONA | |||||||||||||
Full Title: TOFAcitinib plus Hydroxycloroquine vs Hydroxycloroquine in patients with early onset SARS-CoV2 (COVID-19) interstitial pneumonia: a multicenter randomized controlled open label trial | |||||||||||||
Medical condition: SARS-CoV2 related Interstitial Pneumonia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002621-46 | Sponsor Protocol Number: 20878 | Start Date*: 2005-06-27 |
Sponsor Name:University of Nottingham | ||
Full Title: Double-blind, randomised, placebo-controlled trial of nicotine replacement therapy in pregnancy | ||
Medical condition: Smoking during pregnancy Specifically smoking 5 or more cigarettes currently (i.e. whilst pregnant) and having smoked 10 or more cigarettes prior to pregnancy. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-003276-19 | Sponsor Protocol Number: 783 | Start Date*: 2007-11-05 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Efficacy and safety of s- Ketamine and Remifentanil for endovenous analgesy in labour pains | |||||||||||||
Medical condition: endovenous analgesy in labour pains | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003760-36 | Sponsor Protocol Number: HUS277/03/2015 | Start Date*: 2016-01-20 |
Sponsor Name:HUS - Naistentautien ja synnytysten tulosyksikkö | ||
Full Title: Pain an medical abortion -Predicting factors of pain and optimal pain management among teenaged women compared to adult women | ||
Medical condition: Pain during Medical termination of pregnancy | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Female | |
Trial protocol: FI (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000147-13 | Sponsor Protocol Number: I15014 | Start Date*: 2016-06-21 | |||||||||||
Sponsor Name:CHU de LIMOGES | |||||||||||||
Full Title: Is there an interest in repeating the vaginal administration of dinoprostone ( Propess® ) , to promote cervical ripening of pregnant women at term? | |||||||||||||
Medical condition: cervix ripening | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002247-30 | Sponsor Protocol Number: RC31/21/0217 | Start Date*: 2021-09-24 |
Sponsor Name:CHU TOULOUSE | ||
Full Title: Evaluation of Amoxicillin diffusion in breast milk according to a population pharmacokinetic approach. | ||
Medical condition: Breastfeeding | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002544-40 | Sponsor Protocol Number: 5866 | Start Date*: 2014-10-29 |
Sponsor Name:Hôpitaux Universitaires de Strasbourg | ||
Full Title: THE TREATMENT OF HYPERTENSION ASSOCIATED WITH SEVERE PREECLAMPSIA. A RANDOMIZED CONTROLLED TRIAL OF URAPIDIL VERSUS NICARDIPINE. The URANIC trial. | ||
Medical condition: Hypertension associated with severe pre eclampsia | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FR (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005511-11 | Sponsor Protocol Number: SPON1155-12 | Start Date*: 2013-05-07 | ||||||||||||||||||||||||||
Sponsor Name:RACD Cardiff University | ||||||||||||||||||||||||||||
Full Title: Fibrinogen concentrate versus placebo for treatment of postpartum haemorrhage: a prospective double blind randomised control trial | ||||||||||||||||||||||||||||
Medical condition: Postpartum haemorrhage | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-016752-52 | Sponsor Protocol Number: - | Start Date*: 2010-03-24 | |||||||||||
Sponsor Name:BGP Kranj [...] | |||||||||||||
Full Title: Intravensko lajšanje porodnih bolečin z remifentanilom, ki si ga uravnava porodnica sama – primerjava protokola brez uporabe bazalne infuzije in protokola z uporabo bazalne infuzije glede kvalitete... | |||||||||||||
Medical condition: labour pain | |||||||||||||
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Population Age: In utero, Newborns, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SI (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000609-36 | Sponsor Protocol Number: FIFERM03 | Start Date*: 2019-12-16 |
Sponsor Name:Hospital Vall d´Hebrón | ||
Full Title: Study of the use of Liposomal Iron in the treatment of iron deficiency anemia in pregnancy and puerperium | ||
Medical condition: Iron deficiency anemia | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
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