- Trials with a EudraCT protocol (31)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
31 result(s) found for: Osteophytes.
Displaying page 1 of 2.
EudraCT Number: 2005-002735-27 | Sponsor Protocol Number: R30-05-01 | Start Date*: 2005-09-19 |
Sponsor Name:Fidia Farmaceutici SpA | ||
Full Title: A multicentre study to assess the safety and efficacy of sodium hyaluronate (Hyalgan-F) produced by fermentation in knee psteoarthritis. | ||
Medical condition: Knee oasteoarthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: | |
Trial protocol: LV (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-002127-10 | Sponsor Protocol Number: 19-AOI-11 | Start Date*: 2020-09-01 | |||||||||||
Sponsor Name:CHU de Nice | |||||||||||||
Full Title: Evaluation of pain after intra-articular injections of botulinum toxin in carpometacarpal osteoarthritis of the thumb | |||||||||||||
Medical condition: Rhizarthrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005329-11 | Sponsor Protocol Number: FX006-2014-008 | Start Date*: 2015-02-26 | |||||||||||
Sponsor Name:Flexion Therapeutics | |||||||||||||
Full Title: A Double-Blind, Randomized, Single-Dose Study to Assess the Safety and Efficacy of FX006 for the Treatment of Pain in Patients with Osteoarthritis of the Knee | |||||||||||||
Medical condition: Osteoarthritis of the knee | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) LT (Completed) EE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011785-28 | Sponsor Protocol Number: CEN BIOTECH 150309 | Start Date*: 2009-10-12 | |||||||||||
Sponsor Name:SUBSTIPHARM DEVELOPPEMENT | |||||||||||||
Full Title: Multicenter randomized, double blind, 3 parallel arms, controlled trial of the clinical efficacy of topical 'Diclofenac 1%, gel' (diclofenac diethylamine 1.16%) for the treatment of osteoarthritis ... | |||||||||||||
Medical condition: Patient présentant une ostéorthrose douloureuse d'au moins un des genoux. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001028-23 | Sponsor Protocol Number: T1010-01 | Start Date*: 2017-08-02 | ||||||||||||||||
Sponsor Name:Tools4Patient | ||||||||||||||||||
Full Title: Validation Study to Investigate the Effect of T4P1010 treatment in Patients with Osteoarthritic Pain of Knee or Hip. | ||||||||||||||||||
Medical condition: Osteoarthritic pain of knee or hip. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-001151-19 | Sponsor Protocol Number: DKOA21 | Start Date*: 2007-08-21 | |||||||||||
Sponsor Name:Sint Maartenskliniek | |||||||||||||
Full Title: Placebo controlled trial to evaluate the effect on pain and function of six months treatment doxycycline in established knee osteoarthritis | |||||||||||||
Medical condition: Osteoarthritis of the knee, mild to severe pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003939-38 | Sponsor Protocol Number: P160404J | Start Date*: 2017-12-19 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Short-term efficacy of a single ultrasound-guided intra-articular injection of botulinum toxin A associated with splinting for base-of-thumb osteoarthritis on pain at 3 months: A randomized placebo... | |||||||||||||
Medical condition: Patients referred to our Physical Medicine Rehabilitation Department of a tertiary care center in Paris, France, for the management of Base-of-thumb osteoarthritis (BTOA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001096-73 | Sponsor Protocol Number: MIV-711-202 | Start Date*: 2016-09-13 | |||||||||||
Sponsor Name:Medivir AB | |||||||||||||
Full Title: An Open-Label, One-Arm Phase II Extension Study to Evaluate Safety and Tolerability of MIV-711 in Patients with Knee Joint Osteoarthritis | |||||||||||||
Medical condition: Knee Join Osteoarthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002590-44 | Sponsor Protocol Number: 3175A1-202-WW | Start Date*: 2007-01-25 |
Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc, Clinical Research and Development | ||
Full Title: A MULTICENTER, RANDOMIZED, DOUBLE-BLIND COMPARISON OF 4 DOSE REGIMENS OF PLA-695, NAPROXEN, AND PLACEBO ADMINISTERED DAILY FOR 6 WEEKS IN SUBJECTS WITH ACTIVE OSTEOARTHRITIS OF THE KNEE | ||
Medical condition: ACTIVE OSTEOARTHRITIS OF THE KNEE | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) NL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-000515-95 | Sponsor Protocol Number: B3D-EW-GHCX | Start Date*: 2005-06-16 |
Sponsor Name:Eli Lilly and Company Limited | ||
Full Title: Differential Effects of Teriparatide and Strontium Ranelate on Bone Remodeling and Formation in Postmenopausal Women with Osteoporosis: A Histomorphometric Study | ||
Medical condition: Osteoporosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: CZ (Completed) ES (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-001136-37 | Sponsor Protocol Number: CR4056-2-01 | Start Date*: 2015-08-19 | |||||||||||
Sponsor Name:Rottapharm Biotech S.r.l. | |||||||||||||
Full Title: A randomized, double-blind, parallel group, placebo-controlled study to evaluate the efficacy, safety and tolerability of CR4056 administered for 2 weeks in patients with osteoarthritis of the knee... | |||||||||||||
Medical condition: Moderate to severe chronic pain due to knee osteoarthritis with or without neuropathic component. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004805-34 | Sponsor Protocol Number: TDU13828-ACT13830 | Start Date*: 2015-04-02 | |||||||||||
Sponsor Name:Sanofi-aventis Research & Development | |||||||||||||
Full Title: A Two Part Protocol Using Double Blind Placebo Control to Assess the Safety, Tolerability, and Pharmacokinetics of Single Escalating Intra-articular Doses Followed by Assessment of Efficacy, Safety... | |||||||||||||
Medical condition: Osteoarthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023830-22 | Sponsor Protocol Number: AAG-G-H-1102 | Start Date*: 2012-05-23 | |||||||||||
Sponsor Name:TETEC AG | |||||||||||||
Full Title: NDisc Study: A Prospective Randomized Multicentre Phase I / II Clinical Trial to Evaluate Safety and Efficacy of NOVOCART® Disc plus Autologous Disc Chondrocyte Transplantation (ADCT) in the Treatm... | |||||||||||||
Medical condition: The subject has a disc herniation with back and /or leg pain (radicular pain) and an identification for sequestrectomy according to the guidelines of DGNC and DGOOC. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003875-35 | Sponsor Protocol Number: GO-ON-01 | Start Date*: 2009-03-24 | |||||||||||
Sponsor Name:Rottapharm SpA | |||||||||||||
Full Title: Comparative study of efficacy and safety of GO-ON and Hyalgan in patients with symptomatic osteoarthritis of the knee. | |||||||||||||
Medical condition: Patients with symptomatic osteoarthritis of the knee. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002638-19 | Sponsor Protocol Number: 2012GR03 | Start Date*: 2013-10-21 | |||||||||||
Sponsor Name:University of Dundee & NHS Tayside | |||||||||||||
Full Title: The Effect of Spironolactone on Pain in Older People with Osteoarthris | |||||||||||||
Medical condition: Knee osteoarthritis | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003602-26 | Sponsor Protocol Number: CBA106191 | Start Date*: 2007-05-04 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A double-blind, two-period, placebo controlled cross-over study of the effects of the CB2 agonist GW842166 on pain and sensitisation in patients with osteoarthritis. | |||||||||||||
Medical condition: Osteoarthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024320-23 | Sponsor Protocol Number: I4F-EW-CCAC | Start Date*: 2011-03-08 | |||||||||||
Sponsor Name:Chorus, Eli Lilly and Company | |||||||||||||
Full Title: A Proof-of-Concept Study of the Effects of LY2828360 in the Treatment of Patients with Osteoarthritic Knee Pain | |||||||||||||
Medical condition: Pain in osteoarthritic knee. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001970-33 | Sponsor Protocol Number: 167700-002CL | Start Date*: 2013-07-19 | |||||||||||
Sponsor Name:Proximagen Limited | |||||||||||||
Full Title: A Double-Blind, Randomised, Exploratory Study to Investigate the Safety, Efficacy and Pharmacokinetics of PRX167700 in Subjects with Knee Osteoarthritis. | |||||||||||||
Medical condition: Osteoarthritis of the knee | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004641-33 | Sponsor Protocol Number: DIA2020-01 | Start Date*: 2021-02-16 | |||||||||||||||||||||
Sponsor Name:Diakonhjemmet Hospital | |||||||||||||||||||||||
Full Title: The Methotrexate in ERosive INflammatory Osteoarthritis (MERINO) trial | |||||||||||||||||||||||
Medical condition: Norwegian adult males and females with symptomatic erosive inflammatory hand osteoarthritis. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NO (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002793-39 | Sponsor Protocol Number: 0451 | Start Date*: 2018-03-13 | |||||||||||
Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
Full Title: Abatacept Bone Effects in Psoriatic Arthritis with Bone Biomarker – ABEPSA_BB | |||||||||||||
Medical condition: Psoriatic arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
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