- Trials with a EudraCT protocol (4)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
4 result(s) found for: Amniotomy.
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EudraCT Number: 2006-003250-18 | Sponsor Protocol Number: P010606 | Start Date*: 2007-04-05 | |||||||||||
Sponsor Name:Poole Hospital NHS Trust | |||||||||||||
Full Title: A two-centred randomised double blind controlled trial comparing intramuscular diamorphine and intramuscular pethidine for labour analgesia | |||||||||||||
Medical condition: pain relief during active labour | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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 ( PropessĀ® ) , 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: 2015-001548-13 | Sponsor Protocol Number: BRN-C-2015-01 | Start Date*: 2015-09-24 |
Sponsor Name:BOIRONSIH | ||
Full Title: RANDOMIZED DOUBLE-BLIND CLINICAL TRIAL TO MEASURE THE EFFICACY OF ACTAEA RACEMOSA (9CH) AND CAULOPHYLLUM THALICTROIDES (9CH) IN THE FIRST STAGE OF LABOR | ||
Medical condition: First stage of labor | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: View results |
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) |
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