- Trials with a EudraCT protocol (31)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
31 result(s) found for: Umbilical Artery.
Displaying page 1 of 2.
EudraCT Number: 2018-003182-34 | Sponsor Protocol Number: 2018-10 | Start Date*: 2018-10-18 |
Sponsor Name:CHR d'ORLEANS | ||
Full Title: Randomized, double-blind, controlled clinical trial for comparison of continuous phenylephrine versus norepinephrine infusion for maintenance of hemodynamic stability during cesarean section under... | ||
Medical condition: hypotension during caesarean section under spinal anesthesia | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000903-10 | Sponsor Protocol Number: 26022016 | Start Date*: 2017-01-04 |
Sponsor Name:Oulu University Hospital | ||
Full Title: Efficacy and blood concentrations of epidural hydromorphone in labour | ||
Medical condition: Labour pain | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FI (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005979-16 | Sponsor Protocol Number: PrOvAS001 | Start Date*: 2013-04-29 |
Sponsor Name:Instituto de Investigación Sanitaria La Fe | ||
Full Title: PREECLAMPSIA OF PREVENTION IN PATIENTS THROUGH ovodonation aspirin in early gestation | ||
Medical condition: PREECLAMPSIA | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2020-000315-76 | Sponsor Protocol Number: 1375_RCF_MAC | Start Date*: 2021-12-06 | |||||||||||
Sponsor Name:Centro Hospitalar Universitário de Lisboa Central, EPE | |||||||||||||
Full Title: Low molecular weight heparin in the treatment of early fetal growth restriction | |||||||||||||
Medical condition: Early fetal growth restriction | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: PT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004112-63 | Sponsor Protocol Number: DutchSTRIDER | Start Date*: 2014-08-13 |
Sponsor Name:Academic Medical Center | ||
Full Title: The Dutch STRIDER (Sildenafil TheRapy In Dismal prognosis Early-onset intrauterine growth Restriction) Trial | ||
Medical condition: Fetal growth restriction | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003138-18 | Sponsor Protocol Number: UCC-Strider | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:University College Cork | |||||||||||||
Full Title: STRIDER Ireland: A Randomised Controlled Trial of Sildenafil Therapy In Dismal Prognosis Early‐Onset Intrauterine Growth Restriction | |||||||||||||
Medical condition: Severe early - onset Intrauterine Growth Restriction (IUGR), (also referred to as Fetal growth restriction) diagnosed between 22+0 and 29+6 gestational age. IUGR is defined as an estimated fetal we... | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004600-30 | Sponsor Protocol Number: mvdv/er102015 | Start Date*: 2016-01-18 |
Sponsor Name:University Hospitals Leuven | ||
Full Title: Conventional patient controlled epidural analgesia (PCEA) versus programmed intermittent epidural boluses (PIEB) for labor analgesia: a randomized, double blind study in nulliparous women | ||
Medical condition: providing adequate analgesia during labor and child birth | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-002338-19 | Sponsor Protocol Number: BUSCLAB001 | Start Date*: 2019-01-22 |
Sponsor Name:Oslo University Hospital | ||
Full Title: BUSCLAB - A DOUBLE BLIND RANDOMIZED PLACEBO-CONTROLLED TRIAL INVESTIGATING THE EFFECT OF INTRAVENOUS BUTYLSCOPOLAMINE BROMIDE TO TREAT SLOW PROGRESS IN LABOR | ||
Medical condition: To study the effect of Butylscopolamide Bromide on duration of the active phase of first stage of labor in women who cross the alert-line for labor dystocia, according to the WHO partograph. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NO (Completed) | ||
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: 2015-000185-59 | Sponsor Protocol Number: 12012015 | Start Date*: 2015-03-03 | |||||||||||
Sponsor Name:Merja Kokki | |||||||||||||
Full Title: The effect of oxycodone to placental and fetal circulation during the phase I of labor and the efficacy, safety and neonatal effects of oxycodone. | |||||||||||||
Medical condition: Labor pain at the onset of labor in previously healthy women with normal pregnancy | |||||||||||||
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Population Age: In utero, Newborns, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: FI (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005398-32 | Sponsor Protocol Number: STRIDER | Start Date*: 2014-07-18 | |||||||||||
Sponsor Name:Liverpool Women's NHSFT [...] | |||||||||||||
Full Title: A randomised controlled trial of sildenafil therapy in dismal prognosis early-onset intrauterine growth restriction | |||||||||||||
Medical condition: Early onset intrauterine growth restriction | |||||||||||||
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Population Age: | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003730-13 | Sponsor Protocol Number: OST07/11 | Start Date*: 2012-05-22 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | ||||||||||||||||||
Full Title: Effects of plasma expanders administration in pregnancies complicated by intra uterine growth restriction | ||||||||||||||||||
Medical condition: intra uterine growth restriction | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-000622-22 | Sponsor Protocol Number: ASAP | Start Date*: 2012-07-20 | |||||||||||
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | |||||||||||||
Full Title: Aspirin for the enhancement of trophoblastic invasion in women with abnormal uterine artery Doppler at 11-14 weeks of gestation | |||||||||||||
Medical condition: Placental insufficiency | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003181-12 | Sponsor Protocol Number: HOTPOT1 | Start Date*: 2016-10-07 |
Sponsor Name:Royal College of Surgeons in Ireland | ||
Full Title: Can sonographic assessment of pulmonary vascular reactivity following maternal hyperoxygenation therapy predict neonatal outcome in fetuses at risk of pulmonary hypertension? | ||
Medical condition: Persistent pulmonary hypertension of the newborn (PPHN) is a relatively common condition occurring in 7/1000 births and can result in significant cardiovascular instability in the newborn. It occur... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: IE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-001726-22 | Sponsor Protocol Number: COLIGROW | Start Date*: 2022-12-12 | |||||||||||
Sponsor Name:Dr. Ignacio Herraiz García | |||||||||||||
Full Title: COok's ballon versus dinoprostone for Labor Induction of term pregnancies with fetal GROWth restriction (COLIGROW study). | |||||||||||||
Medical condition: Induction of term pregnancies with fetal growth restriction. | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000392-37 | Sponsor Protocol Number: Protocol_version_1_09-02-2021 | Start Date*: 2021-11-02 |
Sponsor Name:Oslo University Hospital | ||
Full Title: A double-blind randomized placebo-controlled four-arm trial to assess the efficacy of oral bicarbonate and intravenous butylscopolamine bromide to facilitate spontaneous (non-operative) delivery in... | ||
Medical condition: Nulliparous women with induction of labor at term and a singleton fetus in vertex position | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NO (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-004692-40 | Sponsor Protocol Number: PPL20 | Start Date*: 2021-03-30 | |||||||||||
Sponsor Name:Dilafor AB | |||||||||||||
Full Title: An Exploratory, Open label, Randomized, Parallel-Group, Pilot Study to evaluate Safety, Tolerability and Efficacy of daily, subcutaneous tafoxiparin treatment from the time of diagnosis for up to 4... | |||||||||||||
Medical condition: Preeclampsia diagnosed at week 26-32 of gestation. | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
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: 2020-001177-78 | Sponsor Protocol Number: APHP191008 | Start Date*: 2021-02-25 | |||||||||||||||||||||
Sponsor Name:University of Utah | |||||||||||||||||||||||
Full Title: Certolizumab to Prevent Pregnancy Complications in High-Risk Patients with APS or SLE | |||||||||||||||||||||||
Medical condition: Pregnant women with Antiphospholipid Syndrom (APS) and Lupus Antocoagulant (LAC) | |||||||||||||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||||||||||||
Trial protocol: FR (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-005031-32 | Sponsor Protocol Number: Diabetes2017 | Start Date*: 2017-10-10 | |||||||||||
Sponsor Name:Pirkanmaan sairaanhoitopiiri | |||||||||||||
Full Title: Metformin use to improve pregnancy outcome in women with type 1 diabetes. A double-blind placebo-controlled multicenter study. | |||||||||||||
Medical condition: Pregnancy of a women dealing with type 1 diabetes | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
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