- Trials with a EudraCT protocol (5)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
5 result(s) found for: Episiotomy.
Displaying page 1 of 1.
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: 2016-002786-62 | Sponsor Protocol Number: CHD065-16 | Start Date*: 2017-04-14 | |||||||||||
Sponsor Name:Centre Hospitalier Départemental Vendée | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004833-10 | Sponsor Protocol Number: EC12/2017 | Start Date*: 2018-01-15 |
Sponsor Name:Fundación para la Investigación Biomédica | ||
Full Title: Clinical trial ramdomized for treatment of perineal pain and dyspareunia portpartum through local anesthetic infiltrations vs anesthetic and corticoids | ||
Medical condition: perineal pain and dyspareunia postpartum | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005512-12 | Sponsor Protocol Number: MVDV | Start Date*: 2007-12-19 |
Sponsor Name:University Hospitals Leuven | ||
Full Title: Een verbetering van de analgesie na episiotomie door epidurale toediening van neostigmine en clonidine. | ||
Medical condition: Combinedn spinal-epidural analgesia during labour. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-002942-30 | Sponsor Protocol Number: 01012015 | Start Date*: 2015-12-10 | ||||||||||||||||
Sponsor Name:Regional Hospital of Randers | ||||||||||||||||||
Full Title: CONDISOX: Continued versus discontinued oxytocin stimulation of labour in a double-blind randomised controlled trial | ||||||||||||||||||
Medical condition: Syntocinon is used for labour induction to stimulate contractions. The current recommendation is to stimulate until delivery. We hypothesize that discontinuation of Syntocinon when the active phase... | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: DK (Completed) NL (Completed) | ||||||||||||||||||
Trial results: View results |
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