- Trials with a EudraCT protocol (37)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
37 result(s) found for: Ankle Injury.
Displaying page 1 of 2.
EudraCT Number: 2017-002185-51 | Sponsor Protocol Number: Poplitea2017 | Start Date*: 2017-10-18 | |||||||||||
Sponsor Name:Tampere University Hospital | |||||||||||||
Full Title: Effect of perineural dexamethasone on the duration of popliteal nerve block for analgesia after ankle surgery | |||||||||||||
Medical condition: Ankle arthrosis, situation after ankle injury or malposition of ankle/foot, arthrodesis as a curative therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (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: 2016-002620-92 | 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: 2011-004496-37 | Sponsor Protocol Number: 0028021 | Start Date*: 2011-11-25 | |||||||||||
Sponsor Name:Orion Pharma | |||||||||||||
Full Title: A RANDOMISED, MULTICENTRE, TWO-ARM, PARALLEL GROUP, DOUBLE-BLIND, PLACEBO-CONTROLLED, COMPARATIVE EFFICACY AND SAFETY CLINICAL STUDY OF IBUPROFEN 5% GEL IN ADULT HUMAN PATIENTS WITH PAIN RELATED TO... | |||||||||||||
Medical condition: Pain related to uncomplicated ankle injuries | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020935-38 | Sponsor Protocol Number: VOSG-P-318 | Start Date*: 2010-12-14 | |||||||||||
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 sodium topical gel 1% applied four times daily in subjects with ... | |||||||||||||
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: 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: 2011-004497-28 | Sponsor Protocol Number: 0028022 | Start Date*: 2011-12-13 | |||||||||||
Sponsor Name:Orion Pharma | |||||||||||||
Full Title: A RANDOMISED, MULTICENTRE, TWO-ARM, PARALLEL GROUP, DOUBLE-BLIND, PLACEBO-CONTROLLED, COMPARATIVE EFFICACY AND SAFETY CLINICAL STUDY OF IBUPROFEN 5% ROLL-ON GEL IN ADULT HUMAN PATIENTS WITH PAIN RE... | |||||||||||||
Medical condition: Pain related to uncomplicaated ankle injuries. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) LT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003797-25 | Sponsor Protocol Number: VOPO-PE-201 | Start Date*: 2007-10-24 | |||||||||||
Sponsor Name:Novartis Consumer Health SA | |||||||||||||
Full Title: A randomized, double-blind, multi-center, vehicle-controlled, parallel group study to evaluate the efficacy and safety of diclofenac diethylamine 2.32% gel applied once or twice daily in subjects w... | |||||||||||||
Medical condition: acute ankle sprain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006465-38 | Sponsor Protocol Number: 21EU-Fpf02 | Start Date*: 2022-06-06 | |||||||||||||||||||||
Sponsor Name:IBSA Institut Biochimique S.A. | |||||||||||||||||||||||
Full Title: A Randomized, Double-Blind, Multi-Centre, Placebo-Controlled, Active Comparator Study to Evaluate the Efficacy and Safety of a diclofenac epolamine (DHEP) 2.6% medicated plaster in the treatment of... | |||||||||||||||||||||||
Medical condition: Acute pain in mild/moderate ankle sprains | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PL (Completed) CZ (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001720-30 | Sponsor Protocol Number: DRO-200/II/14/1 | Start Date*: 2014-09-23 |
Sponsor Name:Drossapharm AG | ||
Full Title: A randomized, double-blind, multi-center, placebo-controlled, parallel group study to evaluate the efficacy and safety of an etofenamate 5% (EFM) cutaneous patch applied twice daily in patients wit... | ||
Medical condition: Ankle sprain, Grade I or II | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-001874-16 | Sponsor Protocol Number: B3491009 | Start Date*: 2015-07-29 |
Sponsor Name:Pfizer | ||
Full Title: Placebo Controlled, Double Blind Evaluation of the Efficacy and Safety of Ibuprofen 5% Topical Gel for the Treatment of Ankle Sprain | ||
Medical condition: First or second degree ankle sprain | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
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: 2016-000252-99 | Sponsor Protocol Number: DRO-200/III/15/1 | Start Date*: 2016-06-08 |
Sponsor Name:Drossapharm AG | ||
Full Title: A randomized, double-blind, multi-center, placebo-controlled, parallel group study to evaluate the efficacy and safety of an etofenamate 5% cutaneous patch applied twice daily in subjects with acut... | ||
Medical condition: Ankle sprain, grade I or II | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001639-35 | Sponsor Protocol Number: M602011014 | Start Date*: 2019-11-26 | |||||||||||
Sponsor Name:Merz Pharmaceuticals GmbH | |||||||||||||
Full Title: Prospective, randomized, double-blind, placebo-controlled, multicenter study to investigate the efficacy and safety of NT 201 in the treatment of lower limb spasticity caused by stroke or traumatic... | |||||||||||||
Medical condition: Diagnosis of lower limb spasticity with or without upper limb spasticity of the same body side caused by stroke or traumatic brain injury | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Ongoing) DE (Restarted) NO (Completed) CZ (Ongoing) GB (GB - no longer in EU/EEA) ES (Ongoing) IT (Restarted) HU (Ongoing) SK (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004792-50 | Sponsor Protocol Number: C1502 | Start Date*: 2017-08-22 |
Sponsor Name:Biologische Heilmittel Heel GmbH | ||
Full Title: Multi-centre, Double-blind, Randomised, Active- and Placebo-Controlled, Confirmatory Trial to Demonstrate Efficacy and Safety of Traumed® Gel in Patients having Acute Ankle Sprain | ||
Medical condition: Acute Ankle Sprain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-011571-71 | Sponsor Protocol Number: VOPO-P-307 | Start Date*: 2009-07-20 |
Sponsor Name:Novartis Consumer Health SA | ||
Full Title: A randomized, double-blind, multi-center, placebo-controlled, 3-treatment arm, parallel group study to evaluate the efficacy and safety of diclofenac diethylamine 2.32% gel applied twice or three t... | ||
Medical condition: ankle sprain Grade I or II | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-001032-99 | Sponsor Protocol Number: DRO-200-III-20-1 | Start Date*: 2020-09-03 |
Sponsor Name:Drossapharm AG | ||
Full Title: Randomized, controlled, double-blind, multi-center trial to evaluate the efficacy and safety of “Lixim 70 mg wirkstoffhaltiges Pflaster” (etofenamate 70 mg medicated plaster) applied once daily (ev... | ||
Medical condition: Acute ankle sprain, Grade I | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-003647-29 | Sponsor Protocol Number: SN-SPAS-202 | Start Date*: 2020-03-23 | |||||||||||
Sponsor Name:Solstice Neurosciences a wholly-owned subsidiary of US WorldMeds, LLC | |||||||||||||
Full Title: A Phase 2/3, Multicenter, Randomized, Double-Blind, Placebo Controlled, Single-Treatment Efficacy and Safety Study of MYOBLOC® in the Treatment of Adult Lower Limb Spasticity Followed by an Open-La... | |||||||||||||
Medical condition: Lower Limb Spasticity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) CZ (Ongoing) PL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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 (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000992-33 | Sponsor Protocol Number: RH01805 | Start Date*: 2013-10-10 | |||||||||||||||||||||
Sponsor Name:GlaxoSmithKline Consumer Healthcare | |||||||||||||||||||||||
Full Title: A Clinical Study to Assess the Efficacy and Onset of Pain Relief of Topical MFC51123 Diclofenac-Menthol Gel versus Controls in Ankle Sprain | |||||||||||||||||||||||
Medical condition: Pain and inflammation due to Grade I or Grade II acute sprain of the lateral ankle | |||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
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