- Trials with a EudraCT protocol (38,831)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
38,831 result(s) found for: $1.
Displaying page 1,491 of 1,942.
| EudraCT Number: 2004-003853-13 | Sponsor Protocol Number: HPEPA-01 | Start Date*: 2005-01-13 |
| Sponsor Name:Hela Pharma AB | ||
| Full Title: Placebo controlled, randomised, double-blind, multicentre study of PlusEPA (a PUFA, Polyunsaturated Fatty Acids, supplement) as treatment for ADHD (combined type) with co-morbidity in Swedish child... | ||
| Medical condition: ADHD (combined type) and co-morbidity in children | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-002887-41 | Sponsor Protocol Number: OV-W05 | Start Date*: 2004-12-01 |
| Sponsor Name:OmniVision GmbH | ||
| Full Title: Randomisierte, kontrollierte, für den Prüfer verblindete klinische Prüfung (Pilotstudie) zur Untersuchung der Wirksamkeit von Spersadex® Augentropfen im Vergleich zu Isopto®-Dex Augentropfen bei Pa... | ||
| Medical condition: Nicht-infektiöse Conjunctivitis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-005020-41 | Sponsor Protocol Number: AMG 001 | Start Date*: 2005-06-06 |
| Sponsor Name:Heinrich Heine Universität Düsseldorf | ||
| Full Title: Topische Anwendung von Tacrolimus (Protopic) bei verschiedenen Formen des kutanen Lupus erythe-matodes im Rahmen einer klinischen Untersuchung an mehreren nationalen Zentren | ||
| Medical condition: kutaner Lupus erythematodes Die Patienten zeigen meist an der Haut erythematöse Plaques im Rahmen dieser Erkrankung, welche häufig im Gesicht auftreten, schmerzempfindlich sind und zentral vernarb... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-003740-22 | Sponsor Protocol Number: A25/04-ZKSD | Start Date*: 2005-04-08 |
| Sponsor Name:PKH-Pharmazeutische Kontroll- und Herstellungslabor GmbH | ||
| Full Title: Doppelblinder, randomisierter, vehikel- und referenzkontrollierter Nachweis der antibakteriellen Wirksamkeit von Kaliumpermanganat(0,001%)-enthaltenden topischen Präparationen zur epikutanen Applik... | ||
| Medical condition: Objective of the trial is the testing of the antibacterial efficacy of a Kaliumpermanaganat (0.001%)-containing topical preparation for cutaneous application in healthy volunteers | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-000558-60 | Sponsor Protocol Number: PX104.1.7-202 | Start Date*: 2005-06-02 |
| Sponsor Name:Pharmexa A/S | ||
| Full Title: A Phase II trial evaluating the immunological and clinical efficacy and safety of HER-2 Protein AutoVac(TM) and Stimulon® Adjuvant QS-21 monotherapy in patients with metastatic breast cancer | ||
| Medical condition: Female patients with histologically proven metastatic or locally advanced breast cancer who have HER-2 overexpression in the primary tumour and/or a metastatic lesion. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: HU (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-002110-38 | Sponsor Protocol Number: 20050506 | Start Date*: 2007-09-12 |
| Sponsor Name:Dept of ped hem/onc | ||
| Full Title: RCT of oral paracetamol for procedural anxiety, distress and pain in children with cancer | ||
| Medical condition: Pain relif before needle insertion in a subcoutanously implanted iv port in children with cancer | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-001363-58 | Sponsor Protocol Number: PPAPR0202 | Start Date*: 2006-11-14 |
| Sponsor Name:Photopharmica Ltd | ||
| Full Title: Phase IIa randomised, placebo controlled trial to investiagte antimicrobial photodynamic therapy in chronic leg ulcers and diabetic foot ulcers. | ||
| Medical condition: Chronic leg ulcers and chronic diabetic foot ulcers | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-004822-29 | Sponsor Protocol Number: CHL1/02-2004 | Start Date*: 2005-03-09 | |||||||||||
| Sponsor Name:SINTETICA SA | |||||||||||||
| Full Title: Spinal anaesthesia with 2 -chlopoprocaine 1% for lower limb procedures of short duration: a prospective randomized, blind, dose-finding study. | |||||||||||||
| Medical condition: Spinal anaesthesia for short therm surgical procedures | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-002850-69 | Sponsor Protocol Number: IGPM01 | Start Date*: 2006-01-06 |
| Sponsor Name:Swansea NHS Trust | ||
| Full Title: Role of High dose insulin and glucose-potassium-magnesium (HDI-GKM) for Myocardial protection in cardiac surgery | ||
| Medical condition: We propose to recruit 90 patients (based on the power calculation) undergoing first time urgent in-house CABG at Morriston Hospital. The decision to operate on an urgent basis will be based on the ... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-001700-39 | Sponsor Protocol Number: IP-REM-PK-01-EU | Start Date*: 2005-09-14 | |||||||||||
| Sponsor Name:Fresenius Biotech GmbH | |||||||||||||
| Full Title: Determination of systemic exposure and characterization of pharmacokinetics of the tri-functional antibody catumaxomab (anti-EpCAM X anti-CD3) administered intraperitoneally in EpCAM positive cance... | |||||||||||||
| Medical condition: epithelial cell adhesion molecule (EpCAM) expressing tumors in patients with malignant ascites requiring therapeutic ascites puncture | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-005222-41 | Sponsor Protocol Number: 04/Q2803/72 | Start Date*: 2005-08-26 |
| Sponsor Name:UHCW NHS Trust | ||
| Full Title: Intrathecal Morphine for pain management in patients undergoing major abdominal surgery: The optimal dose? | ||
| Medical condition: The use of intrathecal morphine for post-operative pain relief following major abdominal surgery - the comparison of two doses (10 micrograms/kg and 20 micrograms/kg) medical condition = post-oper... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-005046-12 | Sponsor Protocol Number: Final protocol | Start Date*: 2005-09-22 |
| Sponsor Name:Ulster Community & Hospitals Trust | ||
| Full Title: A double blind prospective randomised controlled trial to evaluate the effect of topical phenytoin on the healing of venous leg ulcers | ||
| Medical condition: Venous Leg Ulceration | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-002832-93 | Sponsor Protocol Number: TaxAlim01 | Start Date*: 2006-11-16 |
| Sponsor Name:Städt. Krankenhaus Martha Maria Halle | ||
| Full Title: Phase I/II-Studie Kombinationschemotherapie mit Docetaxel und Pemetrexed in der 2nd line-Therapie bei Patienten mit NSCLC, Stadium IIIB und IV | ||
| Medical condition: Nichtkleinzelliges Bronchialkarzinom, Stadium IIIB und IV | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-003806-27 | Sponsor Protocol Number: None avaliable | Start Date*: 2005-10-13 |
| Sponsor Name:Princess Alexandra Hospital | ||
| Full Title: Is potent topical corticosteroid ointment covered by a plastic film dressing more effective than using potent corticosteroid ointment alone in children with atopic dermatitis? | ||
| Medical condition: Children aged 1-15 years with Atopic Dermatitis | ||
| Disease: | ||
| 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: 2005-005469-12 | Sponsor Protocol Number: NEO-012 | Start Date*: 2006-01-06 |
| Sponsor Name:Neolab Limited | ||
| Full Title: A Phase III, randomised, double-blind, double-dummy cross-over study to compare two dry powder inhaled formulations of budesonide on methacholine hyper-reactivity in patients with stable, persisten... | ||
| Medical condition: Stable, persistent, moderate asthma | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-005263-29 | Sponsor Protocol Number: 25-01 | Start Date*: 2006-01-31 |
| Sponsor Name:Gesellschaft fuer klinische Forschung e.V. (Society for Clinical Research) [...] | ||
| Full Title: Multiple Sclerosis and Extract of Cannabis (MUSEC): A randomised, double-blind, placebo-controlled phase III trial to determine the efficacy and safety of a standardised oral extract of Cannabis sa... | ||
| Medical condition: Multiple Sclerosis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-001696-19 | Sponsor Protocol Number: TTD 04-01 | Start Date*: 2005-01-26 |
| Sponsor Name:Spanish Cooperative Group for Gastrointestinal Tomour therapy | ||
| Full Title: Open-label, phase II, multicentre study on cetuximab treatment as first-line monotherapy in elderly patients with metastatic colorectal cancer expressing EGFR | ||
| Medical condition: Epidermal Growth Factor Receptor-expressing in metatstatic colorrectal cancer in first line treatment. | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-001210-33 | Sponsor Protocol Number: UHL 10054 | Start Date*: 2006-06-20 |
| Sponsor Name:University Hospitals of Leicester NHS Trust | ||
| Full Title: A cohort study of anticholinergic drugs in South Asian women with detrusor overactivity | ||
| Medical condition: The medical condidtion is overactive bladder . A wide range of different anticholinergic agents is available to treat overactive bladder (OAB) symptoms. Within the last 15 years, ethno-pharmacologi... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-000785-39 | Sponsor Protocol Number: KETO 02/04 | Start Date*: 2005-09-21 | |||||||||||
| Sponsor Name:MIPHARM | |||||||||||||
| Full Title: Efficacy and Tolerability of Ketomousse, Ketoconazole 1 , Salicilic Acid and Zinc phyritione thermolabile foam in the treatment of Pityriasis Versicolor in comparison with Ketoconazole 2 cream ... | |||||||||||||
| Medical condition: PITYRIASIS VERSICOLOR | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-005645-19 | Sponsor Protocol Number: 20051130 | Start Date*: 2007-09-12 |
| Sponsor Name:Dept of ped hem/onc | ||
| Full Title: RCT of oral ibuprofen for procedural anxiety, distress and pain in children with cancer | ||
| Medical condition: Pain and anxiety relief before needle insertion in a subcutanously implanted iv port in children with cancer. | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
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