- Trials with a EudraCT protocol (9)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
9 result(s) found for: Forceps Delivery.
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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: 2015-005247-14 | Sponsor Protocol Number: CHUB-Equidol | Start Date*: 2016-08-09 |
Sponsor Name:Centre Hospitalier Universitaire Brugmann | ||
Full Title: Effect of levobupivacaine infiltration versus placebo on perineal postpartum pain in episiotomy of primiparous, after instrumental delivery: randomized double blind clinical trial. | ||
Medical condition: Episiotomy (inclusion of primiparous patients giving birth by instrumental delivery -Suzor forceps, vacuum extraction, Thierry spatulas with episiotomy). | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
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: 2016-000889-35 | Sponsor Protocol Number: CHUB-PIB | Start Date*: 2016-05-26 |
Sponsor Name:Centre Hospitalier Universitaire Brugmann | ||
Full Title: Comparison of two methods of administration of the epidural, by programmed intermittent bolus or continuous perfusion, on the incidence of instrumented deliveries and cesareans in primiparous women. | ||
Medical condition: Fist child delivery with epidural | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-000872-89 | Sponsor Protocol Number: MK001 | Start Date*: 2015-10-29 |
Sponsor Name:University of Oxford | ||
Full Title: ANODE: a randomised controlled trial of prophylactic ANtibiotics to investigate the prevention of infection following Operative vaginal DElivery. | ||
Medical condition: Maternal infection in the first six weeks after operative vaginal delivery. | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-000145-40 | Sponsor Protocol Number: versiĆ³n2.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: 2019-000620-17 | Sponsor Protocol Number: PPL17 | Start Date*: 2019-05-08 | |||||||||||
Sponsor Name:Dilafor AB | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Proof of Concept Study (section A) with a conditional dose finding follow up (Section B) to Evaluate the Efficacy on Cervical ripening... | |||||||||||||
Medical condition: Induction of labor in pregnant women with unripe cervix | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000770-29 | Sponsor Protocol Number: Ireland-RctV8 | Start Date*: 2018-06-18 | ||||||||||||||||
Sponsor Name:The Rotunda Hospital | ||||||||||||||||||
Full Title: Investigating the role of early low-dose aspirin in diabetes: A phase III multicentre double-blinded placebo-controlled randomised trial of low-dose aspirin initiated in the first trimester of diab... | ||||||||||||||||||
Medical condition: Pregestational type I or type II diabetes | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: IE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
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) |
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