- Trials with a EudraCT protocol (5)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (10)
5 result(s) found for: Stress fractures.
Displaying page 1 of 1.
EudraCT Number: 2014-004318-27 | Sponsor Protocol Number: stressfrakturogbisfosfonat | Start Date*: 2016-08-31 |
Sponsor Name:Oslo University Hospital | ||
Full Title: Intravenous bisphosphonate in stress fracture treatment -A randomised controlled double blinded multicenter trial | ||
Medical condition: Stress fractures in the foot | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002130-20 | Sponsor Protocol Number: 1.4 | Start Date*: 2020-02-07 | ||||||||||||||||
Sponsor Name:Norfolk and Norwich University Hospitals NHS Foundation Trust | ||||||||||||||||||
Full Title: Research on Efficacy of Teriparatide use in the Return of recruits to Normal duty. | ||||||||||||||||||
Medical condition: Healthy individuals with stress fractures. | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005093-40 | Sponsor Protocol Number: CS I-040202/01 | Start Date*: 2007-10-22 | |||||||||||
Sponsor Name:Kuros Biosurgery AG | |||||||||||||
Full Title: A phase II randomized, controlled, open-labeled (dose-blinded) dose finding study of the safety and efficacy of I-040202 in the treatment of patients with acute open tibial shaft fractures | |||||||||||||
Medical condition: Acute open tibial shaft fractures | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) HU (Completed) SI (Completed) FI (Completed) CZ (Completed) SK (Completed) IT (Completed) BG (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005030-73 | Sponsor Protocol Number: AVD111960 | Start Date*: 2009-11-11 | |||||||||||
Sponsor Name:GlaxoSmithKline | |||||||||||||
Full Title: Thiazolidinedione Intervention with vitamin D Evaluation (TIDE) A Multicenter Randomized Double-Blind Placebo-Controlled Trial of a Thiazolidinedione or Placebo and of Vitamin D or Placebo In Peopl... | |||||||||||||
Medical condition: - Incidence of CV outcomes compared to placebo for the TZD class as a whole, rosiglitazone (RSG), and pioglitazone (PIO) when added to the therapeutic regimen of a person with type 2 diabetes who h... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) CZ (Prematurely Ended) NL (Completed) DE (Completed) DK (Prematurely Ended) SK (Prematurely Ended) FR (Prematurely Ended) LV (Prematurely Ended) IE (Completed) IT (Prematurely Ended) FI (Completed) GB (Prematurely Ended) GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001749-42 | Sponsor Protocol Number: 484/12 | Start Date*: 2012-08-07 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Effects of treatment and withdrawal with inhaled beclomethasone/formoterol on lung inflammation in COPD. | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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