- Trials with a EudraCT protocol (228)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
228 result(s) found for: Osteoarthritis, Knee AND Pain.
Displaying page 12 of 12.
EudraCT Number: 2005-002691-15 | Sponsor Protocol Number: Jointcare/Fe/1/DK | Start Date*: 2006-02-16 |
Sponsor Name:Ferrosan A/S | ||
Full Title: Ginger, ginger-avokado-soy, glucosamine sulfate and ginger-ibuprofen in relation to chronic low back pain - a randomised double-blind, placebo-controlled clinical trial with parallel groups for 3 m... | ||
Medical condition: Chronic low back pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-003482-14 | Sponsor Protocol Number: KF5503/24-R331333-PAI-3007 | Start Date*: 2007-02-23 | |||||||||||
Sponsor Name:Johnson & Johnson Pharamceutical Resarch & Development, L.L.C | |||||||||||||
Full Title: A One-Year, Randomized, Open-Label, Parallel-Arm, Phase III Long-Term Safety Trial, with Controlled Adjustment of Dose, of Multiple Doses of CG5503 PR* and Oxycodone CR in Subjects with Chronic Pain | |||||||||||||
Medical condition: Chronic pain due to knee or hip osteoarthritis or low back pain of benign origin | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) NL (Completed) AT (Completed) BE (Completed) GB (Completed) SK (Completed) SI (Prematurely Ended) FR (Completed) CZ (Completed) DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001691-21 | Sponsor Protocol Number: GR-OG-279239-02 | Start Date*: 2016-05-17 | |||||||||||
Sponsor Name:Genera Research Ltd | |||||||||||||
Full Title: SAFETY, TOLERABILITY, rhBMP6 PHARMACOKINETICS AND BONE HEALING EFFECT OF A SINGLE DOSE OF OSTEOGROW (rhBMP6 IN AUTOLOGOUS WHOLE BLOOD COAGULUM DERIVED [WBCD] CARRIER) IN ADULT PATIENTS TREATED BY H... | |||||||||||||
Medical condition: Osteoarthritis of the medial knee joint compartment and/or symptomatic varus deformity. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000503-33 | Sponsor Protocol Number: 01-05 | Start Date*: 2005-09-02 |
Sponsor Name:Department Integrative Medicine, Kliniken Essen Mitte | ||
Full Title: Effectiveness of leech therapy in osteoarthritis of the thumb joint (rhizarthrosis) - a randomized controlled trial | ||
Medical condition: Leeches therapy has been successully evaluated in symptomatic knee osteoarthrits for pain relief. In the planned study patients with painful rhizarthrosis (arthrosis of the thumb joint) will be rec... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-016816-20 | Sponsor Protocol Number: cod16HS14 | Start Date*: 2010-05-24 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:co.don AG | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Prospective, randomised, open label, multicentre Phase II clinical trial to investigate the efficacy and safety of the treatment of large defects (4-10 cm2) with 3 different doses of the autologous... | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Cartilage defects of knee joints, osteochondral defects | |||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-002581-35 | Sponsor Protocol Number: CL-033-II-02 | Start Date*: 2007-09-25 | |||||||||||
Sponsor Name:IDEA AG | |||||||||||||
Full Title: Multiple dose, double-blind, double-dummy, placebo and active controlled study of pharmacokinetics of Diractin® as well as safety and efficacy for the treatment of muscle soreness from exercise | |||||||||||||
Medical condition: The study population is a healthy population who are voluntarily participating in this clinical trial. This study will compare the PK profile after e.c. and oral application of the same dosage of ... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004469-11 | Sponsor Protocol Number: PP-SA-001 | Start Date*: 2022-01-11 |
Sponsor Name:PHERECYDES PHARMA | ||
Full Title: PhagoDAIR I: A Phase I/II Multicenter, Randomized, Double-Blind Study to Evaluate Efficacy and Safety of Phage Therapy in Patients with Hip or Knee Prosthetic Joint Infection due to Staphylococcus ... | ||
Medical condition: knee or hip prosthetic joint infection (PJI) due to Staphylococcus aureus, with the indication of DAIR and Suppressive Antibiotics Therapy (SAT | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001633-41 | Sponsor Protocol Number: SONIA2 | Start Date*: 2013-09-17 | |||||||||||
Sponsor Name:University of Liverpool (UniLiv) | |||||||||||||
Full Title: An international, multicenter, randomized, evaluator-blinded, no-treatment controlled, parallel-group study to assess the efficacy and safety of once daily nitisinone in patients with alkaptonuria ... | |||||||||||||
Medical condition: Alkaptonuria (AKU) - a serious, autosomal recessive, multisystem disorder. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) SK (Completed) | |||||||||||||
Trial results: (No results available) |
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