- Trials with a EudraCT protocol (4)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
4 result(s) found for: Amniotic sac.
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EudraCT Number: 2007-004506-27 | Sponsor Protocol Number: 07-029 | Start Date*: 2007-12-20 | |||||||||||
Sponsor Name:CHU de CAEN | |||||||||||||
Full Title: Intérêt de la tocolyse dans la prise en charge des ruptures prématurées des membranes entre 24 et 34 semaines d’aménorrhée. | |||||||||||||
Medical condition: premature rupture of membranes | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
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 (Prematurely Ended) | |||||||||||||
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: 2022-003124-41 | Sponsor Protocol Number: 219510 | Start Date*: 2023-03-27 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals SA | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 3b, non-randomized, open label, multi-country, cohort study to describe the safety of study participants who received RSVPreF3 maternal vaccination (any dose) or controls from previous RSV ... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Pregnancy related outcomes and events in maternal participants who were vaccinated against RSV or received control, and in their infants | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: FI (Completed) BE (Completed) DE (Completed) FR (Ongoing) ES (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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