- Trials with a EudraCT protocol (42)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (75)
42 result(s) found for: Heel.
Displaying page 1 of 3.
EudraCT Number: 2006-002749-35 | Sponsor Protocol Number: 0881A3-404 | Start Date*: 2007-04-13 | |||||||||||
Sponsor Name:Wyeth Pharmaceuticals France | |||||||||||||
Full Title: A Multicentre, Double-Blind, Placebo-Controlled, Randomized Study of Etanercept in the Treatment of Adults Patients with Refractory Heel Enthesitis in Spondylarthropathy | |||||||||||||
Medical condition: Refractory heel enthesitis in spondylarthropathy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) FR (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000972-91 | Sponsor Protocol Number: CAIN457F3301 | Start Date*: 2016-07-05 | ||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
Full Title: A randomized, double-blind, placebo-controlled multicenter study of subcutaneous secukinumab to demonstrate efficacy in the treatment of enthesitis at the Achilles tendon up to 1 year in adult pati... | ||||||||||||||||||
Medical condition: Psoriatic arthritis Axial spondyloarthritis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) GB (Completed) ES (Completed) SK (Completed) CZ (Completed) GR (Completed) BG (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003237-25 | Sponsor Protocol Number: POPPIV4.022.07.16 | Start Date*: 2015-08-21 |
Sponsor Name:University of Oxford | ||
Full Title: A blinded randomised placebo-controlled trial investigating the efficacy of morphine analgesia for procedural pain in infants | ||
Medical condition: Screening for Retinopathy of Prematurity is an essential yet painful routine test that is performed multiple times in infants who are born prematurely. Premature infants also regularly require heel... | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2008-003666-26 | Sponsor Protocol Number: AREM07 | Start Date*: 2010-01-12 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE NIGUARDA CA` GRANDA (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: A double-blind, randomized trial of ARNICA comp.-Heel treatment in patients undergoing hemorrhoidectomy in day surgery: evaluation of postoperative pain | |||||||||||||
Medical condition: patients undergoing hemorrhoidectomy in day surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
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: 2005-003942-32 | Sponsor Protocol Number: NXEEG-05/01 | Start Date*: 2005-12-12 |
Sponsor Name:Biologische Heilmittel Heel GmbH | ||
Full Title: | ||
Medical condition: Sleep disturbances and nervous states of restlessness | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-000575-32 | Sponsor Protocol Number: 1 | Start Date*: 2018-12-18 | |||||||||||
Sponsor Name:Isabel Maria Ruiz | |||||||||||||
Full Title: Results of the injection of botulinum toxin vs platelet rich plasma for the treatment of plantar fasciitis | |||||||||||||
Medical condition: Plantar fasciitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007939-41 | Sponsor Protocol Number: TRS-ESP | Start Date*: 2009-04-13 |
Sponsor Name:Biologische Heilmittel Heel GmbH, | ||
Full Title: ESTUDIO DOBLE CIEGO, ALEATORIZADO, MULTICÉNTRICO SOBRE LA EFICACIA DE TRAUMEEL® S (POMADA Y GEL), EN TÉRMINOS DE DOLOR Y FUNCIÓN, COMPARADO CON UN AINE TÓPICO EN DEPORTISTAS CON ESGUINCE DE TOBILLO... | ||
Medical condition: Analgesia y antinflamatorio en esguince de tobillo | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-001802-32 | Sponsor Protocol Number: C1501 | Start Date*: 2015-08-14 | |||||||||||
Sponsor Name:Biologische Heilmittel Heel GmbH | |||||||||||||
Full Title: Neuronal correlates of Neurexan® action in mildly to moderately stressed probands - a randomized, placebo-controlled, double-blind, cross-over trial of mode of action and response prediction by fun... | |||||||||||||
Medical condition: mildly to moderately stressed probands | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005421-40 | Sponsor Protocol Number: RCSI-1764 | Start Date*: 2016-06-14 | |||||||||||||||||||||||||||||||
Sponsor Name:Royal College of Surgeons in Ireland | |||||||||||||||||||||||||||||||||
Full Title: The use of topical Glyceryl Trinitrate (GTN) and eccentric exercises in the treatment of mid portion Achilles Tendinopathy: a randomised placebo controlled trial | |||||||||||||||||||||||||||||||||
Medical condition: Achilles tendinopathy | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: IE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-002896-17 | Sponsor Protocol Number: V1.17.05.2013 | Start Date*: Information not available in EudraCT |
Sponsor Name:Orthopädisches Spital Speising | ||
Full Title: Functional evaluation of two therapy concepts: dynamic orthoses and BoNT | ||
Medical condition: Infantile cerebral palsy | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001257-18 | Sponsor Protocol Number: 16400076 | Start Date*: 2008-07-14 |
Sponsor Name:Biomet Nederland BV | ||
Full Title: Use of PRP to treat plantar fasciitis, blinded and randomized as a multi center study | ||
Medical condition: Patients with plantar fasciitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-002358-22 | Sponsor Protocol Number: C1201 | Start Date*: 2012-08-06 | |||||||||||
Sponsor Name:Biologische Heilmittel Heel GmbH | |||||||||||||
Full Title: NEUPRO DB, efficacy profile of Neurexan in an experimental acute stress setting – an explorative double blind study in healthy probands | |||||||||||||
Medical condition: Neurexan to be effective in fostering mental balance by reducing tension and nervousness during acute stress setting in healthy probands | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002359-40 | Sponsor Protocol Number: C1202 | Start Date*: 2012-07-18 | |||||||||||
Sponsor Name:Biologische Heilmittel Heel GmbH | |||||||||||||
Full Title: NEUPRO OL, Efficacy profile of Neurexan® in an experimental acute stress setting – an explorative open-label study in healthy probands | |||||||||||||
Medical condition: Neurexan to be effective in fostering mental balance by reducing tension and nervousness during acute stress setting in healthy probands | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003087-20 | Sponsor Protocol Number: 800_OPBG_2014 | Start Date*: 2014-11-12 | |||||||||||||||||||||
Sponsor Name:IRCCS Ospedale Pediatrico Bambino Gesù | |||||||||||||||||||||||
Full Title: Determination of Plasmatic and CSF Levels Of High Doses Of Micafungin in Neonates Suffering from Systemic Candidiasis and/or Candida meningitis. | |||||||||||||||||||||||
Medical condition: Systemic Candidiasis and/or Candida Meningitis | |||||||||||||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-000821-74 | Sponsor Protocol Number: KKS-MS-006KMT-01/06 | Start Date*: 2006-12-08 | |||||||||||
Sponsor Name:University Hospital of Muenster | |||||||||||||
Full Title: A randomized. double-blind, placebo-controlled, phase III trial for the efficacy of Traumeel S in the prevention and treatment of chemotherapie-induced Mucositis in Patients undergoing allogeneic s... | |||||||||||||
Medical condition: Treatment of chemotherapie-induced oral mucositis | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003393-12 | Sponsor Protocol Number: TRARO | Start Date*: 2013-03-19 | |||||||||||||||||||||
Sponsor Name:Biologische Heilmittel Heel GmbH | |||||||||||||||||||||||
Full Title: Treatment of rotator cuff syndrome and bursitis: A double blind, controlled trial to assess the efficacy and safety of Traumeel® S injection versus corticosteroid injections and versus placebo | |||||||||||||||||||||||
Medical condition: rotator cuff syndrome and bursitis | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) BE (Completed) ES (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-005197-78 | Sponsor Protocol Number: 1 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Queen's Medical Centre, Nottingham, University Hospital NHS Trust, | |||||||||||||
Full Title: A multi-centre, randomised, parallel group, cross-over study comparing the efficacy and safety of double versus multiple injections of Botulinum Toxin type-A (Dysport®), into the gastrocnemius musc... | |||||||||||||
Medical condition: Spasticity of the Gastrocnemius Muscle due to Cerebral Palsy | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005043-86 | Sponsor Protocol Number: 1308143 | Start Date*: 2014-03-21 | |||||||||||
Sponsor Name:CHU de Saint-Etienne | |||||||||||||
Full Title: Reactivity of the autonomic nervous system after a nociceptive stress in the newborn: Interest of sucrose and non-nutritive sucking. | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Newborns, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005128-18 | Sponsor Protocol Number: CS I – 020201/01 | Start Date*: 2009-03-20 | |||||||||||
Sponsor Name:Kuros Biosurgery AG | |||||||||||||
Full Title: A randomized, multi-center, controlled, parallel group, dose finding study of the efficacy and safety of topically applied I-020201 as an adjunct to good standard-of-care versus good standard-of-ca... | |||||||||||||
Medical condition: Chronic diabetic foot ulcers | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) CZ (Completed) | |||||||||||||
Trial results: (No results available) |
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