- Trials with a EudraCT protocol (87)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
87 result(s) found for: Form perception.
Displaying page 1 of 5.
EudraCT Number: 2005-004452-13 | Sponsor Protocol Number: A6121127 | Start Date*: 2005-12-16 | |||||||||||
Sponsor Name:Pfizer Inc. | |||||||||||||
Full Title: A Randomized, Double Blind, Placebo Controlled Detrol La "Add-On" To Alpha-Blocker Study in men with persistent Overactive Bladder symptoms of urinary frequency and urgency with/without urgency inc... | |||||||||||||
Medical condition: Overactive Bladder in Men | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: SK (Completed) ES (Completed) DK (Completed) GB (Completed) SE (Completed) IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004711-23 | Sponsor Protocol Number: DT11/9936 | Start Date*: 2013-05-22 |
Sponsor Name:Leeds Dental Institute | ||
Full Title: Comparative studies of the anaesthetic efficacy of 4% Articaine used as mandibular infiltration versus 2% Lidocaine used as inferior dental nerve block, in extraction and pulpotomy of mandibular pr... | ||
Medical condition: Dental caries in primary molars | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-024181-22 | Sponsor Protocol Number: A0221095 | Start Date*: 2011-05-18 | |||||||||||
Sponsor Name:Pfizer Inc.235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A 12-WEEK, PHASE 4, RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED, PARALLEL GROUP, MULTICENTER TRIAL IN OVERACTIVE BLADDER SUBJECTS TO CONFIRM THE EFFICACY OF 8 MG FESOTERODINE COMPARED TO 4 MG F... | |||||||||||||
Medical condition: Overactive Bladder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) CZ (Completed) HU (Completed) DE (Completed) FI (Completed) GR (Completed) LT (Completed) AT (Completed) DK (Completed) SK (Completed) BG (Prematurely Ended) NO (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023175-26 | Sponsor Protocol Number: P_TPT_2010 | Start Date*: 2011-01-14 | |||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||
Full Title: Influence of Tapentadol on endogenous modulation of pain in chronic neuropathic pain patients and healthy volunteers | |||||||||||||
Medical condition: Chronic pain patients/ mhealthy volunteers | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000996-33 | Sponsor Protocol Number: A6121122 | Start Date*: 2004-08-04 |
Sponsor Name:Pfizer AB | ||
Full Title: A global phase IV, double-blind, placebo-controlled, randomized trial to evaluate the effectiveness of Detrusitol SR 4 mg on Patient's Perception of Bladder Condition (PPBC). | ||
Medical condition: Overactive bladder syndrome (OAB) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) GB (Completed) IT (Completed) DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-000129-76 | Sponsor Protocol Number: BTXSENS | Start Date*: 2007-04-27 | |||||||||||
Sponsor Name:Guy's & St Thomas' NHS Foundation Trust | |||||||||||||
Full Title: Botulinum toxin-A in Sensory Urgency | |||||||||||||
Medical condition: Sensory Urinary Urgency. This is a condition where patients have urinary urgency (sudden desire to urinate which cannot be deferred) /- urge incontinence (urine leakage) and usually is accompanied ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002979-17 | Sponsor Protocol Number: MANCOR | Start Date*: 2014-01-27 |
Sponsor Name:IVI Sevilla | ||
Full Title: Comparative study between the usage of corifollitropin alfa and daily recombinant FSH in the ovarian stimulation of low responders | ||
Medical condition: Low response to ovarian stimulation | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2004-002894-21 | Sponsor Protocol Number: CDAR328A2409 | Start Date*: 2005-06-21 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A 12-week, randomized, double-blind, placebo-controlled, parallel group, multicenter study to evaluate the efficacy, safety and tolerability of darifenacin (7.5 mg o.d. with voluntary up-titration... | ||
Medical condition: Overactive bladder (OAB) | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) SE (Completed) HU (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-000143-12 | Sponsor Protocol Number: ORBIS-DE-UNIBO001 | Start Date*: 2019-07-25 | |||||||||||
Sponsor Name:ALMA MATER STUDIORUM UNIVERSITà DI BOLOGNA | |||||||||||||
Full Title: OXYTOCIN RESEARCH FOR BEHAVIORAL IMPAIRMENT SYMPTOMS IN DEMENTIA: Potential clinical efficacy of intranasal oxytocin in the treatment of frontotemporal dementia. A randomized, double-blind, placebo... | |||||||||||||
Medical condition: Frontotemporal dementia (bvFTD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004249-16 | Sponsor Protocol Number: F02207GE204 | Start Date*: 2005-02-02 |
Sponsor Name:PIERRE FABRE MEDICAMENT | ||
Full Title: THE EFFECT OF MILNACIPRAN 100MG BID ON SENSITIVITY TO STIMULUS-EVOKED PAIN IN PATIENTS WITH FIBROMYALGIA: A FMRI NEUROIMAGING STUDY | ||
Medical condition: Fibromyalgia is a chronic disorder characterized by widespread musculoskeletal pain, widespread tenderness and fatigue. The disorder is well defined in the USA, where the current diagnosis of FMS i... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) SE (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-024179-18 | Sponsor Protocol Number: A0221094 | Start Date*: 2011-05-31 | |||||||||||
Sponsor Name:Pfizer Inc.235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A 14 WEEK RANDOMIZED PARALLEL GROUP PLACEBO-CONTROLLED DOUBLE-BLIND MULTICENTRE STUDY OF FESOTERODINE 8 MG IN OVERACTIVE BLADDER PATIENTS WITH SUB-OPTIMAL RESPONSE TO TOLTERODINE 4 MG ER | |||||||||||||
Medical condition: Overactive Bladder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) HU (Completed) DE (Completed) CZ (Completed) FI (Completed) GR (Completed) BG (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006957-29 | Sponsor Protocol Number: DUBAR01 | Start Date*: 2007-08-02 |
Sponsor Name:Department of Psychiatry and Psychotherapy, Friedrich-Schiller-University Jena | ||
Full Title: Influence of Duloxetin on C-fiber function and perception of deep somatic pain in major depression | ||
Medical condition: We aim to achieve a study population of 30 patients (male or female, 18 to 65 years of age) suffering from major depressive disorder (DSM IV criteria). Depressive symptoms should be present for at ... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-012393-12 | Sponsor Protocol Number: IPR-MET-7 | Start Date*: 2009-09-11 |
Sponsor Name:Laboratoires IPRAD | ||
Full Title: Essai comparatif, multicentrique, prospectif, randomisé, en double insu, d’efficacité et de tolérance de Météoxane® versus placebo dans la poussée douloureuse du syndrome de l'intestin irritable | ||
Medical condition: Irritable bowel syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005255-17 | Sponsor Protocol Number: | Start Date*: 2014-09-05 |
Sponsor Name:University of Leeds | ||
Full Title: Chronotherapeutic lifestyle intervention for diabetes and obesity to reset the circadian rhythm and improve cardiometabolic risk in the European population | ||
Medical condition: first-degree relatives of individuals with type 2 diabetes. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-001684-11 | Sponsor Protocol Number: mentholmarch08 | Start Date*: 2008-06-19 | |||||||||||
Sponsor Name:University of Edinburgh | |||||||||||||
Full Title: A Pilot Study into the Effect of Topical Menthol for Patients with Neuropathic-Type Pain. | |||||||||||||
Medical condition: The condition under investigation is neuropathic-type pain. This may be due to a variety of causes including malignant neuropathic-type pain (such as tumour-related nerve compression or cancer-rel... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013431-38 | Sponsor Protocol Number: UF 8546 | Start Date*: 2009-11-20 | |||||||||||
Sponsor Name:CHRU Montpellier | |||||||||||||
Full Title: Etude ouverte prospective randomisée sur l’utilisation du Flammacérium® dans les nécroses cutanées ischémiques du pied | |||||||||||||
Medical condition: Nécrose cutanée ischémique du pied | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000700-14 | Sponsor Protocol Number: 2 | Start Date*: 2019-07-08 |
Sponsor Name:Medical University Graz | ||
Full Title: Pilot-Study comparing analgosedation concepts during placement of regional anaesthesia with either fentanyl, remifentanil, clonidine, EMLA-Patch or placebo in regard of patient's wellbeing, pain an... | ||
Medical condition: Patient with elective orthopedic surgery that will be administered a regional anaesthesia will be subject of the investigation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-004994-25 | Sponsor Protocol Number: CSMS995A2101 | Start Date*: 2008-02-04 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multi-center, randomized, double-blind, placebo-controlled, crossover study in women with irritable bowel syndrome to evaluate feasibility and reproducibility of barostat assessments of colorecta... | |||||||||||||
Medical condition: Irritable Bowel Syndrom | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006176-30 | Sponsor Protocol Number: NW-1029/01-08 | Start Date*: 2009-03-13 | |||||||||||
Sponsor Name:Newron Pharmaceuticals S.p.A. | |||||||||||||
Full Title: EFFICACY AND SAFETY OF TWO FIXED DOSES (160 OR 320 MG/DAY) OF RALFINAMIDE IN PATIENTS WITH CHRONIC NEUROPATHIC LOW BACK PAIN. A MULTICENTER, DOUBLE-BLIND, RANDOMISED, PLACEBO-CONTROLLED 12- WEEK ST... | |||||||||||||
Medical condition: Chronic neuropathic low back pain. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) DE (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003436-74 | Sponsor Protocol Number: 01-18/629-15 | Start Date*: 2019-07-10 | |||||||||||
Sponsor Name:Intas Pharmaceuticals Ltd | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-controlled, Three-arm, Parallel Assignment, Multi-Centre, Therapeutic Equivalence Study of Two Fluorouracil 5% Topical Cream Formulations in Adult Pat... | |||||||||||||
Medical condition: Actinic Keratosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) RO (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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