- Trials with a EudraCT protocol (97)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
97 result(s) found for: Musculoskeletal Injury.
Displaying page 1 of 5.
EudraCT Number: 2013-004140-32 | Sponsor Protocol Number: PRP-MUSCULO-2014-01 | Start Date*: 2014-04-28 | |||||||||||
Sponsor Name:Unidad de Cirugia Artroscópica | |||||||||||||
Full Title: CLINICAL STUDY TO ASSES THERAPEUTIC USE OF PLATELET RICH PLASMA IN ACUTE MUSCLE INJURIES IN ELITE ATHLETES" | |||||||||||||
Medical condition: Acute Muscle Injury Type 3A-3B (Munich classification) or type II (Classification of Otto Chan), confirmed by radiological diagnosis and clinical agreement. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000788-30 | Sponsor Protocol Number: 1.2022 | Start Date*: 2023-04-13 |
Sponsor Name:Uzdrowisko Kamień Pomorski S.A. | ||
Full Title: Evaluation of the effectiveness of Methocarbamol in the treatment of spasticity in people with spinal cord injury. | ||
Medical condition: | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-024641-71 | Sponsor Protocol Number: 071(D)SC10102 | Start Date*: 2011-05-12 | |||||||||||
Sponsor Name:ANGELINI | |||||||||||||
Full Title: A randomized, multicenter, double-blind study assessing the efficacy and safety of two topical 10% naproxen gel formulations in the treatment of benign soft-tissue injuries. | |||||||||||||
Medical condition: Benign soft-tissue injuries. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (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: 2011-006270-13 | Sponsor Protocol Number: XCEL-MEN-01 | Start Date*: 2013-01-08 | |||||||||||
Sponsor Name:Banc de Sang i Teixits | |||||||||||||
Full Title: A phase I-IIa safety and efficacy pilot clinical trial of intraarticular administration of autologous mesenchymal stem cells in meniscus injury | |||||||||||||
Medical condition: Degenerative meniscal lesion | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004886-15 | Sponsor Protocol Number: MTA:CT4-09-18--Sponsor:18I-Fsg08 | Start Date*: 2019-05-17 | |||||||||||
Sponsor Name:IBSA INSTITUT BIOCHIMIQUE SA | |||||||||||||
Full Title: Evaluation of Treatment Satisfaction, Effectiveness and Tolerability in Subjects treated with Low-dose Diclofenac Epolamine Soft Capsules for Acute, Mild or Moderate Musculoskeletal Pain | |||||||||||||
Medical condition: Patients with acute, mild or moderate musculoskeletal pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-005165-49 | Sponsor Protocol Number: PLX-HF-01 | Start Date*: 2018-09-24 | |||||||||||
Sponsor Name:Pluristem Ltd. | |||||||||||||
Full Title: A Phase III, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study, Designed to Determine the Efficacy, Safety, and Tolerability of Intramuscular Administration of Allogeneic PLX-PAD Cell... | |||||||||||||
Medical condition: Muscle Injury Following Arthroplasty for Hip Fracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (GB - no longer in EU/EEA) DK (Completed) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001056-19 | Sponsor Protocol Number: HUPA-EC-02-2012 | Start Date*: 2013-12-01 | |||||||||||
Sponsor Name:FUNDACIÓN PARA LA INVESTIGACIÓN BIOMÉDICA DEL HOSPITAL UNIVERSITARIO PRÍNCIPE DE ASTURIAS | |||||||||||||
Full Title: ROLE OF BIOLOGICAL THERAPY IN ROTATOR CUFF TENDINOPATHY. EFFECTIVENESS OF PLASMA RICH IN GROWTH FACTOR (PRGF-ENDORET)REGARDING TO FUNCTIONAL CAPACITY AND PAIN COMPARED WITH THE CONVENTIONAL TREATME... | |||||||||||||
Medical condition: ROTATOR CUFF TENDINOPATHY | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005574-11 | Sponsor Protocol Number: Pennsaid-2014/P-3-01 | Start Date*: 2015-06-18 | |||||||||||
Sponsor Name:Nuvo Research GmbH | |||||||||||||
Full Title: A randomized, double-blind, multi-center, placebo-controlled, parallel group study to evaluate the efficacy and safety of an Diclofenac 2% (w/w) cutaneous solution applied twice daily in patients w... | |||||||||||||
Medical condition: Treatment of pain and Inflammation associated Acute Soft Tissue Injury/Ankle Sprain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002991-28 | Sponsor Protocol Number: N/A | Start Date*: 2016-10-24 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: GRASP: Getting it Right: Addressing Shoulder Pain. Clinical and cost effectiveness of progressive exercise compared to best practice advice, with or without corticosteroid injection, for the treat... | |||||||||||||
Medical condition: Rotator Cuff Partial Tear (not full tear) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002620-92 | Sponsor Protocol Number: Pennsaid-C-2016/P-3-02 | Start Date*: 2016-10-07 | |||||||||||
Sponsor Name:Nuvo Pharmaceuticals Inc. | |||||||||||||
Full Title: A multi-centre, randomised, controlled, double-blind, parallel-group study on the efficacy and safety of Pennsaid-2% topical skin solution in patients with Grade I-II ankle sprain | |||||||||||||
Medical condition: Treatment of pain and Inflammation associated Acute Soft Tissue Injury/Ankle Sprain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (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: 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: 2011-005368-55 | Sponsor Protocol Number: SM1-UG-11 | Start Date*: 2012-01-26 | |||||||||||
Sponsor Name:Professor Joergen Berg Dahl | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2013-000381-11 | Sponsor Protocol Number: NL42823.018.13 | Start Date*: 2013-05-17 | ||||||||||||||||||||||||||
Sponsor Name:Academisch Medisch Centrum | ||||||||||||||||||||||||||||
Full Title: Paracetamol or NSAID's in acute musculoskeletal syndromes | ||||||||||||||||||||||||||||
Medical condition: acute musculoskeletal syndromes | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-005577-23 | Sponsor Protocol Number: 853-P-401 | Start Date*: 2012-07-09 | |||||||||||
Sponsor Name:Novartis Consumer Health | |||||||||||||
Full Title: A randomized, double-blind, multi-center, placebo-controlled, parallel group study to evaluate the efficacy and safety of diclofenac potassium 25 mg in subjects with acute joint pain | |||||||||||||
Medical condition: ankle sprain, grade I - II | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002129-39 | Sponsor Protocol Number: XC.ROD.2017 | Start Date*: 2017-08-02 | |||||||||||
Sponsor Name:XCELL Medical Solutions | |||||||||||||
Full Title: Phase II Clinical Trial to Know the effectiviness and safety with a a treatment based in a therapy with serical autologous white cells versus the use of Platelet Rich Plasma in patients with rotu... | |||||||||||||
Medical condition: Patients with Rotulian Tendinopathy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004057-25 | Sponsor Protocol Number: RC21/18 | Start Date*: 2019-10-02 | |||||||||||
Sponsor Name:IRCCS MATERNO INFANTILE BURLO GAROFOLO | |||||||||||||
Full Title: Oral Ibuprofene versus oral kethorolac for children with musculoskeletal injury: a double blind randomized controlled study. | |||||||||||||
Medical condition: Pain is present in 78% of overall accesses in pediatric emergency rooms and, in most cases, it is acute and secondary to musculoskeletal trauma. Fifthy percent of patients report moderate to severe... | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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 (Ongoing) DE (Completed) IT (Completed) | ||
Trial results: (No results available) |
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