- Trials with a EudraCT protocol (5)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
5 result(s) found for: Uterine sound.
Displaying page 1 of 1.
EudraCT Number: 2016-000424-25 | Sponsor Protocol Number: 1508175 | Start Date*: 2016-04-12 | |||||||||||||||||||||
Sponsor Name:CHU Saint-Etienne | |||||||||||||||||||||||
Full Title: Low-molecular-weight heparin in constituted vascular intrauterine growth restriction. Randomized multicenter trial | |||||||||||||||||||||||
Medical condition: Intrauterine growth restriction (IUGR) | |||||||||||||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||||||||||||
Trial protocol: FR (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001830-32 | Sponsor Protocol Number: RC31/17/0448 | Start Date*: 2019-12-18 |
Sponsor Name:University Hospital Toulouse | ||
Full Title: Phase III Trial to assess impact of ultra-long versus long down-regulation protocol on IVF/ICSI outcomes in infertile women presenting with adenomyosis. | ||
Medical condition: Infertilty in women with adenomyosis. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FR (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-002065-37 | Sponsor Protocol Number: BAY86-5028 / 14371 | Start Date*: 2011-09-12 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: Multi-center, single-arm study to assess the safety, efficacy, discontinuation rate and pharmacokinetics of the low-dose levonorgestrel intrauterine contraceptive system (LCS12) in post-menarcheal ... | |||||||||||||
Medical condition: Contraception | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) NL (Completed) AT (Completed) BE (Completed) DE (Completed) DK (Completed) NO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000287-29 | Sponsor Protocol Number: 1 | Start Date*: 2018-03-23 |
Sponsor Name:Karolinska Institutet | ||
Full Title: Immediate versus delayed insertion of intrauterine contraception at the time of medical abortion An open-label, randomized, multicenter study | ||
Medical condition: Post medical abortion contraception | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004715-37 | Sponsor Protocol Number: M-34273-46 | Start Date*: 2015-04-09 | |||||||||||
Sponsor Name:AstraZeneca AB; Karlebyhus, Astraallén, Södertälje SE-151 85, Sweden | |||||||||||||
Full Title: A randomised, double blind, placebo controlled, parallel study to assess the benefits of aclidinium bromide in the relief of COPD symptoms including cough when administered to patients with COPD | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) HU (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
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