- Trials with a EudraCT protocol (26)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
26 result(s) found for: Contusion.
Displaying page 1 of 2.
EudraCT Number: 2004-000088-92 | Sponsor Protocol Number: F7CBI-1600 | Start Date*: 2004-08-23 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A Randomised, Double-Blind, Placebo-Controlled, Multi-centre, Dose Escalation Study to Evaluate the Safety and Preliminary Efficacy of Recombinant Factor VIIa (NovoSeven®/Niastase®) with Brain Cont... | |||||||||||||
Medical condition: Contusive Brain Injury | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003858-24 | Sponsor Protocol Number: 252BN201 | Start Date*: 2019-08-13 | |||||||||||
Sponsor Name:Biogen Idec Research Limited | |||||||||||||
Full Title: A Multicenter, Double-Blind, Multidose, Placebo-Controlled, Randomized, Parallel-Group, Phase 2 Study to Evaluate the Efficacy and Safety of Intravenous BIIB093 for Patients with Brain Contusion | |||||||||||||
Medical condition: Brain contusion | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020936-21 | Sponsor Protocol Number: VOSG-P-319 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Novartis Consumer Health S.A. | |||||||||||||
Full Title: A randomized, double-blind, multi-center, placebo-controlled, parallel group study to evaluate the efficacy and safety of diclofenac sodium topical gel 1% applied four times daily in subjects with ... | |||||||||||||
Medical condition: Acute blunt soft tissue injuries/contusions of the limbs | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001909-41 | Sponsor Protocol Number: 5070197 | Start Date*: 2008-04-11 | ||||||||||||||||||||||||||
Sponsor Name:Stepani Bendel | ||||||||||||||||||||||||||||
Full Title: Hydrokortisonihoito elinluovutuspotilailla (HYDRO) | ||||||||||||||||||||||||||||
Medical condition: Tutkittavilla on vakava aivovamma ja/tai lukinkalvonalainen verenvuoto, eikä heitä voida parantaa sairaudestaan. Heitä hoidetaan teho-osastolla mahdollisina elintenluovutuspotilaina. | ||||||||||||||||||||||||||||
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Population Age: | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-001779-29 | Sponsor Protocol Number: EP-DICLO/G-01-2015 | Start Date*: 2016-12-15 |
Sponsor Name:Epifarma s.r.l. | ||
Full Title: Randomized, double-blind, parallel group, placebo-controlled, multicenter clinical trial to evaluate efficacy and safety of diclofenac 1% gel produced by Epifarma s.r.l. (Test) versus the originato... | ||
Medical condition: Patients with acute painful and flogistic (inflammatory) disease due to acute traumatic events (injury/contusion) of joints, muscles, tendons and ligaments | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) DE (Completed) IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-002550-30 | Sponsor Protocol Number: DM/PR/5000/003/05 | Start Date*: 2006-11-09 |
Sponsor Name:Chiesi Farmaceutici S. p. A. | ||
Full Title: A randomized controlled pilot study for the comparison of efficacy of bronchoalveolar lavage (BAL) with Curosurf® in a dosage 50 mg/kg vs not treated control in adult patients affected by pulmonary... | ||
Medical condition: lung contusion | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-004102-42 | Sponsor Protocol Number: EP-DICLO/2G-01-2015 | Start Date*: 2017-06-06 | |||||||||||
Sponsor Name:Epifarma S.r.l. | |||||||||||||
Full Title: Randomized, multi-center, double-blind, three-armed trial, to evaluate the non-inferiority, efficacy and safety of diclofenac2% gel (Test) versus the originator diclofenac2% gel chosen as Referenc... | |||||||||||||
Medical condition: Acute traumatic events (injury/contusion) classified from mild to moderate pain at rest to the joints, muscles, tendons and ligaments | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) LV (Completed) LT (Completed) HU (Ongoing) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005165-14 | Sponsor Protocol Number: TK-254R-0201 | Start Date*: 2021-03-25 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Teikoku Seiyaku Co Ltd. | ||||||||||||||||||||||||||||||||||||||
Full Title: Randomized, controlled, double-blind, multi-center trial to evaluate the | ||||||||||||||||||||||||||||||||||||||
Medical condition: Acute strains, sprains or bruises of the extremities following blunt trauma | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-005381-35 | Sponsor Protocol Number: EP-DICLO/G-04-2012 | Start Date*: 2013-06-20 | |||||||||||
Sponsor Name:EPIFARMA SRL | |||||||||||||
Full Title: Randomized, double-blind, placebo-controlled, parallel group, multi-centre clinical trial to evaluate safety and efficacy of Diclofenac 1% gel vs. placebo gel in patients with acute traumatic blunt... | |||||||||||||
Medical condition: Patients with acute traumatic blunt soft tissue injury/contusion of the limbs. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003526-32 | Sponsor Protocol Number: EQI7-16-02 | Start Date*: 2018-08-14 |
Sponsor Name:Fidia Farmaceutici S.p.A. | ||
Full Title: Randomised, double blind, parallel-groups, non-inferiority versus Flector® and superiority versus Placebo, Phase III clinical trial with Diclofenac Sodium 140 mg medicated plaster in patients with ... | ||
Medical condition: Patients with painful and phlogistic (inflammatory response) disease due to acute traumatic events (injury/contusion) of the limbs | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) HU (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-003257-29 | Sponsor Protocol Number: NL1208 | Start Date*: 2013-02-06 | |||||||||||
Sponsor Name:Reckitt Benckiser Healthcare (UK) | |||||||||||||
Full Title: A randomised, double-blind, multi-centre, placebo controlled parallel group study to evaluate the efficacy and tolerability of a new Ibuprofen patch in patients with acute sports related traumatic ... | |||||||||||||
Medical condition: Acute sports-related traumatic blunt soft tissue injury/contusion to the upper or lower limbs | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005661-20 | Sponsor Protocol Number: SKP-021-01-11 | Start Date*: 2012-07-13 | |||||||||||
Sponsor Name:PROMO INTERNATIONAL SRL | |||||||||||||
Full Title: A double-blind, randomised, parallel group, active controlled, multicentre study to assess the therapeutic non-inferiority of SKP-021, a 0.3% ketoprofen patch, versus diclofenac sodium patch in pat... | |||||||||||||
Medical condition: patients with painful and inflammatory conditions (e.g.: back pain, bruise, contusion, sprain, strains) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000888-26 | Sponsor Protocol Number: DEV 1477-2 DIC 05 | Start Date*: 2005-11-07 | |||||||||||
Sponsor Name:ratiopharm GmbH | |||||||||||||
Full Title: Randomised, double-blind, multi-centre, placebo-controlled clinical dose finding study in four parallel groups comparing Diclofenac Gel 1 %, Diclofenac Gel 3 %, Diclofenac Gel 5 % and placebo Gel i... | |||||||||||||
Medical condition: Male or female ambulant patients (age range 18-60 years) suffering from fresh impact injuries (traumatic blunt soft tissue injury/contusion). Time elapse between traumatic event and inclusion must ... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-018018-21 | Sponsor Protocol Number: NL0910 | Start Date*: 2010-06-09 | |||||||||||
Sponsor Name:Reckitt Benckiser Healthcare UK | |||||||||||||
Full Title: A randomised, double-blind, multi-centre, placebo controlled parallel group study to evaluate the efficacy and tolerability of a new Ibuprofen patch in patients with acute sports related traumatic ... | |||||||||||||
Medical condition: Acute sports-related traumatic blunt soft tissue injury/contusion | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013864-37 | Sponsor Protocol Number: 71231 | Start Date*: 2010-02-05 | |||||||||||
Sponsor Name:Gedeon Richter Plc. | |||||||||||||
Full Title: A randomized, multicenter, double-blind, parallel study to compare the efficacy and safety profile of RGH-507 (tolperisone-containing) gel versus a ketoprofen-containing gel in the treatment of pat... | |||||||||||||
Medical condition: acute soft tissue injury minor traumatism (such as: sprain, strain, dislocation,...etc.) or contusion | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-018017-40 | Sponsor Protocol Number: NL0919 | Start Date*: 2010-06-09 | |||||||||||
Sponsor Name:Reckitt Benckiser Healthcare UK Ltd | |||||||||||||
Full Title: A randomised, double-blind, multi-centre, placebo controlled parallel group study to evaluate the efficacy and tolerability of a new Ibuprofen gel in patients with acute sports-related traumatic bl... | |||||||||||||
Medical condition: Acute sports-related traumatic blunt soft tissue injury/contusion | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003829-31 | Sponsor Protocol Number: 05DCz/FHp11 | Start Date*: 2006-01-18 |
Sponsor Name:IBSA Institut Biochimique S.A. | ||
Full Title: A multicentre, prospective, double-blind, in parallel groups randomised, versus placebo and versus reference product controlled, confirmatory clinical trial of the efficacy and tolerance of Flector... | ||
Medical condition: mild-to-moderate contusions | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-012338-56 | Sponsor Protocol Number: VAS203/II/1/03 | Start Date*: 2009-07-10 | |||||||||||
Sponsor Name:vasopharm GmbH | |||||||||||||
Full Title: AN EXPLORATIVE PHASE IIa STUDY TO ASSESS SAFETY, TOLERABILITY, PHARMACODYNAMICS AND PHARMACOKINETICS OF VAS203 IN PATIENTS WITH MODERATE AND SEVERE TRAUMATIC BRAIN INJURY | |||||||||||||
Medical condition: Moderate and severe traumatic brain injury | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FR (Completed) ES (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003778-30 | Sponsor Protocol Number: DRO-200/III/21/1 | Start Date*: 2021-12-29 |
Sponsor Name:Drossapharm AG | ||
Full Title: Randomized, controlled, multi-center trial to evaluate the efficacy and safety of Lixim 70 mg wirkstoffhaltiges Pflaster (etofenamate 70 mg medicated plaster) vs. placebo in the local symptomatic a... | ||
Medical condition: Acute strains, sprains or bruises of soft tissues following blunt trauma, e.g. sports injuries | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001038-32 | Sponsor Protocol Number: 48-03LXPU | Start Date*: 2019-10-15 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Lead Chemical Company Ltd | ||||||||||||||||||||||||||||||||||||||
Full Title: Randomized, controlled, double-blind, multi-center trial to evaluate the efficacy and safety of a Loxoprofen sodium 60 mg tape medicated plaster vs. placebo in the local symptomatic and short-term ... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Acute blunt, soft tissue injuries of the limbs | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
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