- Trials with a EudraCT protocol (688)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
688 result(s) found for: Musculoskeletal pain.
Displaying page 1 of 35.
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: 2008-003596-46 | Sponsor Protocol Number: 942/08 | Start Date*: 2009-02-25 | ||||||||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | ||||||||||||||||||
Full Title: Multicenter, not-for-profit clinical study, in a open, controlled, randomized fashion to compare tolerability, safety and efficacy of two different treatment strategies for non malignant, persisten... | ||||||||||||||||||
Medical condition: non neoplastic cronic pain | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004682-32 | Sponsor Protocol Number: 2011-09 | Start Date*: 2012-02-07 | |||||||||||
Sponsor Name:FONDAZIONE ISTITUTO SAN RAFFAELE-G.GIGLIO | |||||||||||||
Full Title: Intra-articular injection of botulinum toxin type A in hemiplegic shoulder pain: a multicentric, double blind randomised, versus steroid study. | |||||||||||||
Medical condition: hemiplegic shoulder pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (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: 2013-002928-16 | Sponsor Protocol Number: 811700 | Start Date*: 2013-12-24 |
Sponsor Name:F.Schreuder | ||
Full Title: vitamin D and nonspecific musculoskeletal pain in non-Wesren immigrants | ||
Medical condition: nonspecific musculoskeletal complaints | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-018975-13 | Sponsor Protocol Number: ROSA_10 | Start Date*: 2010-02-24 | |||||||||||
Sponsor Name:ISTITUTO ORTOPEDICO RIZZOLI | |||||||||||||
Full Title: EFFICACY OF ROSE HIP IN TREATMENT OF PAIN IN PATIENTS WITH COXARTHROSIS | |||||||||||||
Medical condition: PATIENTS TO BE IMPLANTED WITH HIP PROSTHESIS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005357-23 | Sponsor Protocol Number: 01 | Start Date*: 2013-01-27 | |||||||||||
Sponsor Name:AUSL VITERBO | |||||||||||||
Full Title: Preventing injection pain by Clostridium Histolyticum Collagenase Administration for teatment of Dupuytrens contracture | |||||||||||||
Medical condition: Dupuytren s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003185-33 | Sponsor Protocol Number: INRCA-02-2011 | Start Date*: 2011-10-13 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE DI RICOVERO E CURA PER ANZIANI IRCCS | |||||||||||||
Full Title: Prospective, controlled, randomized, blind study to evaluate the effects of intramuscular-paravertebral injections of an oxygen-ozone (O2-O3) mixture in patients with lumbar pain aged 65 or older | |||||||||||||
Medical condition: subjects aged 65 or older with lumbar pain and discopathy for at least 6 weeks | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2007-003372-18 | Sponsor Protocol Number: NERI-AS001-07 | Start Date*: 2007-12-03 | |||||||||||
Sponsor Name:ABIOGEN PHARMA | |||||||||||||
Full Title: A randomised, double-blind, placebo controlled study to assess the safety and the efficacy of neridronate 100 mg - 4 i.v. infusions in a course of 10 days treatment - in patients with algodystrophi... | |||||||||||||
Medical condition: Algodystrophic Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003513-40 | Sponsor Protocol Number: Bupi-Cata-TYKS-version 1.0. | Start Date*: 2006-08-21 | |||||||||||
Sponsor Name:Kalevi Pihlajamäki | |||||||||||||
Full Title: Intrathecal bupivacaine and clonidine for ambulatory knee arthroscopy | |||||||||||||
Medical condition: Patients are submitted for ambulatory knee arthroscopy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001064-27 | Sponsor Protocol Number: s55283 | Start Date*: 2013-06-25 |
Sponsor Name:University Hospitals Leuven | ||
Full Title: Placebo-controlled trial with vitamin D to prevent worsening/relieve aromatase inhibitor-induced musculoskeletal symptoms in breast cancer patients | ||
Medical condition: aromatase inhibitor-induced musculoskeletal symptoms in postmenopausal breast cancer patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: BE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-004258-24 | Sponsor Protocol Number: FBA | Start Date*: 2011-09-19 | |||||||||||
Sponsor Name:UNIVERSITA' CAMPUS BIOMEDICO | |||||||||||||
Full Title: Clinical trial to study application of MESNA for infiltration into the epidural ''Failed Back Syndrome'' (FBS) | |||||||||||||
Medical condition: Failed Back Syndrome | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004890-25 | Sponsor Protocol Number: BOLD01 | Start Date*: 2013-01-14 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA S. MARIA DELLA MISERICORDIA DI UDINE | |||||||||||||
Full Title: Botulinum Toxin Serotype A randomized double-blind, placebo controlled multicentre study for degenerative coxarthrosis. | |||||||||||||
Medical condition: coxarthrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022794-34 | Sponsor Protocol Number: 862-P-201 | Start Date*: 2011-03-04 | |||||||||||
Sponsor Name:Novartis Consumer Health | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multi-center parallel group phase IV study to evaluate the efficacy and safety of Voltaren® Schmerzgel 1.16% gel in subjects with acute neck pain | |||||||||||||
Medical condition: Acute neck pain, present for at least 12 hours. An acute condition is defined as pain shorter than 3 months [CPMP, 2002]. Neck pain is defined as stiffness and/or pain felt dorsally in the cervical... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018600-87 | Sponsor Protocol Number: Peri-Trauma | Start Date*: 2010-02-24 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA` DI NOVARA | |||||||||||||
Full Title: POST-OPERATIVE PAIN CONTROL OF PEDIATRIC PATIENTS UNDERWENT ORTHOPEDIC SURGERY: COMPARISON OF INTRAVENOUS ANALGESIA AND ONE-SHOT EPIDURAL LUMBAR NERVE BLOCK. | |||||||||||||
Medical condition: POST-OPERATIVE PAIN CONTROL OF PEDIATRIC PATIENTS UNDERWENT ORTHOPEDIC SURGERY | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000487-27 | Sponsor Protocol Number: 0663-806 | Start Date*: 2004-08-10 | |||||||||||
Sponsor Name:Merck Sharp & Dohme (Sweden) AB | |||||||||||||
Full Title: A Double-Blind, Parallel-Group, 4-week Trial to Assess the Efficacy and Safety of Etoricoxib 60mg and Diclofenac 150mg in Patients with Chronic Low Back Pain | |||||||||||||
Medical condition: Chronic Low Back Pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) HU (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003082-15 | Sponsor Protocol Number: KTB-002 | Start Date*: 2011-09-08 | ||||||||||||||||
Sponsor Name:Karen Toftdahl Bjørnholdt | ||||||||||||||||||
Full Title: High dose dexamethasone for pain following arthroscopic shoulder surgery: A randomised blinded clinical trial. | ||||||||||||||||||
Medical condition: Pain following arthroscopic shoulder surgery. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000147-27 | Sponsor Protocol Number: TH/RCT2/0001 | Start Date*: 2012-07-30 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: A Single-Blind Randomised Controlled Pilot trial of Corticosteroid Injection for Shoulder Pain | |||||||||||||
Medical condition: Rotator cuff tendinopathy Adhesive capsulitis of the shoulder joint | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019109-40 | Sponsor Protocol Number: XC0409 | Start Date*: 2011-03-25 | |||||||||||
Sponsor Name:Xenome Ltd | |||||||||||||
Full Title: A multicenter, randomized, observer-blinded, single-dose, placebo-controlled, sequential cohort study of the efficacy and safety of Xen2174 in subjects following bunionectomy surgery | |||||||||||||
Medical condition: Moderate to severe acute post-operative pain in subjects following primary unilateral first metatarsal bunionectomy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: (No results available) |
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