- Trials with a EudraCT protocol (9)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
9 result(s) found for: Interventional pain management.
Displaying page 1 of 1.
| EudraCT Number: 2010-019694-15 | Sponsor Protocol Number: ML25252 | Start Date*: 2010-09-28 | |||||||||||
| Sponsor Name:N.V. Roche S.A. | |||||||||||||
| Full Title: Act-Alone : An open-label, single-arm study to describe glucocorticoid use in rheumatoid arthritis patients treated with Tocilizumab in daily clinical practice and to evaluate systematic glucocorti... | |||||||||||||
| Medical condition: Rheumatoid Arthritis in adult | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-007987-40 | Sponsor Protocol Number: KetaminaEsse | Start Date*: 2008-12-29 | ||||||||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA` DI NOVARA | ||||||||||||||||||
| Full Title: Low dose intravenous ketamine (S) associated to thoracic epidural analgesia: effects on the post-thoracotomy pain syndrome (PTPS) | ||||||||||||||||||
| Medical condition: All patients that will undergo to an elective thoracotomic surgery in the Hospital Maggiore della Carita` of Novara for a 12 months period. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2013-004711-50 | Sponsor Protocol Number: 9785-MA-1001 | Start Date*: 2014-11-24 | |||||||||||
| Sponsor Name:Astellas Pharma Europe Ltd | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase IIIb Study of the Efficacy and Safety of Continuing Enzalutamide in Chemotherapy Naïve Metastatic Castration Resistant Prostate Cancer Patients... | |||||||||||||
| Medical condition: Metastatic Castrate Resistant Prostate Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: CZ (Completed) IT (Completed) GB (GB - no longer in EU/EEA) DE (Completed) SE (Prematurely Ended) ES (Prematurely Ended) GR (Completed) BE (Completed) FR (Completed) AT (Ongoing) PL (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-003544-37 | Sponsor Protocol Number: ABUHB/01/0816/1 | Start Date*: 2016-11-30 | ||||||||||||||||||||||||||
| Sponsor Name:Aneurin Bevan University Health Board | ||||||||||||||||||||||||||||
| Full Title: Perineural Local Anaesthetic Catheter aftEr Major lowEr limb amputatioN Trial (PLACEMENT) | ||||||||||||||||||||||||||||
| Medical condition: Analgesia for lower limb amputation for peripheral vascular disease (PVD) | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2015-000730-30 | Sponsor Protocol Number: R1788 | Start Date*: 2015-05-21 |
| Sponsor Name:Hull and East Yorkshire Hospitals NHS Trust | ||
| Full Title: A randomised clinical trial comparing endovenous laser ablation and mechanochemical ablation (ClariVein®) in the management of superficial venous insufficiency. | ||
| Medical condition: Varicose veins (VVs) or Superficial Venous Insufficiency (SVI) of the legs results from inflammation mediated damage to vein structure, allowing reverse flow. SVI affects 30% of adults and is assoc... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-000411-10 | Sponsor Protocol Number: 4478944789 | Start Date*: Information not available in EudraCT | |||||||||||||||||||||||||||||||
| Sponsor Name:BG-Kliniken Bergmannsheil, Dept. of Pain Management | |||||||||||||||||||||||||||||||||
| Full Title: Effects of Pregabalin on mechanical hyperalgesia - EPOM | |||||||||||||||||||||||||||||||||
| Medical condition: patients with pain for at least 6 months and hyperalgesia with one of the following diagnoses: peripheral nerve lesion, plexus lesion, radicular lesion, spinal lesion, polyneuropathy, postzosteric ... | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: DE (Ongoing) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2016-004820-41 | Sponsor Protocol Number: MK-7625A-035 | Start Date*: 2017-08-23 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
| Full Title: A Phase 2, Randomized, Active Comparator-Controlled, Multicenter, Double-Blind Clinical Trial to Study the Safety and Efficacy of Ceftolozane/Tazobactam (MK-7625A) Plus Metronidazole Versus Meropen... | |||||||||||||
| Medical condition: Complicated intra-abdominal infection (cIAI) | |||||||||||||
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| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: LT (Completed) ES (Completed) HU (Completed) Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-023211-34 | Sponsor Protocol Number: | Start Date*: 2011-04-27 | ||||||||||||||||
| Sponsor Name:University Hospitals of Leicester NHS Trust | ||||||||||||||||||
| Full Title: Randomized Controlled Trial Comparing Intracoronary Administration of Adenosine or Sodium Nitroprusside to Control for Attenuation of Microvascular Obstruction During Primary Percutaneous Coronary ... | ||||||||||||||||||
| Medical condition: Acute ST-segment Elevation Myocardial Infarction | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2014-005079-10 | Sponsor Protocol Number: TOK-200-15 | Start Date*: 2015-07-14 | |||||||||||
| Sponsor Name:Tokai Pharmaceuticals Inc | |||||||||||||
| Full Title: ARMOR3-SV: A Phase 3, Randomized, Open-Label, Multi-Center, Controlled Study of Galeterone Compared with Enzalutamide in Men Expressing Androgen Receptor Splice Variant-7 mRNA with Metastatic Cast... | |||||||||||||
| Medical condition: Androgen receptor (AR) splice variant-7 (ARV7), metastatic (M1) castration resistant prostate cancer (CRPC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: BE (Completed) GB (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
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Query did not match any studies.