- Trials with a EudraCT protocol (375)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (5)
375 result(s) found for: Perception.
Displaying page 1 of 19.
| EudraCT Number: 2009-014717-27 | Sponsor Protocol Number: 2009/4:7 | Start Date*: 2009-12-22 |
| Sponsor Name:Karolinska Institutet/Södersjukhuset | ||
| Full Title: Betametasone as postoperative pain treatment for knee arthroscopies at a day surgical center | ||
| Medical condition: Unspecified knee pain investigated by an arthroscopy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-004864-24 | Sponsor Protocol Number: COPD-1 | Start Date*: 2013-07-09 |
| Sponsor Name:Bionorica SE | ||
| Full Title: Randomized, placebo-controlled, double-blind, cross-over trial with Bronchipret and Sinupret to evaluate acceleration of mucociliary clearance (MCC) | ||
| Medical condition: PR1: Acceleration of mucociliary clearance as a therapeutic effect when treating inflammation of the nasal sinuses PR2: Acceleration of mucociliary clearance as a therapeutic effect when treating ... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-006561-32 | Sponsor Protocol Number: OxyCog-01 | Start Date*: 2009-11-05 |
| Sponsor Name:LWL University Hospital Bochum | ||
| Full Title: Effects of intranasal application of oxytocin on empathy and mentalising in patients with psychotic disorders and severe personality disorders | ||
| Medical condition: Schizophrenia, bipolar disorder, major depression, personality disorder | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-004600-35 | Sponsor Protocol Number: Modifast3 | Start Date*: 2012-12-19 |
| Sponsor Name:KULeuven | ||
| Full Title: Effect of diet-induced weight loss on motilin, ghrelin, bitter taste perception, hunger and the migrating motor complex: a prospective study | ||
| Medical condition: Gastrointestinal contractility and hormones will be studied in obese patients before and after weight loss induced by a diet | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-004369-16 | Sponsor Protocol Number: MJ/LPGB/12/2006 | Start Date*: 2007-11-29 |
| Sponsor Name:St Raphael's Hospice, Surrey | ||
| Full Title: ''Evaluation of the efficacy of 'TRANS-DERMAL NITRATE' in reducing the severity of 'death-rattle' (i.e 'terminal lung secretions' ) in patients dying from end stage malignancy'' | ||
| Medical condition: 'Death-rattle' (i.e 'terminal lung secretions') in adult patients dying from end-stage malignancy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-005334-22 | Sponsor Protocol Number: 347PUNCIOHEMODIALISIS | Start Date*: 2016-05-31 |
| Sponsor Name:HOSPITAL DE PALAMÓS | ||
| Full Title: CLINICAL TRIAL FOR THE TREATMENT OF PAIN IN HEMODIALYSIS PUNCTURE WITH LIDOCAINE / PRILOCAINE, VERSUS CHLOROETHYL, CROSSOVER RANDOMIZED STUDY | ||
| Medical condition: Hemodialysis is the most commonly used therapy for renal replacement being the arteriovenous fistula used for vascular access . Venipuncture in patients causes stress, pain and anxiety. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-019938-27 | Sponsor Protocol Number: OMEGA | Start Date*: 2010-04-27 |
| Sponsor Name:FONDAZIONE CENTRO S. RAFFAELE DEL MONTE TABOR | ||
| Full Title: Input of tact and kinestesia in strength perception. | ||
| Medical condition: healthy volunteers enrolled to study kinestesia with an psychophysical approach | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: IT (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-001318-39 | Sponsor Protocol Number: UNIHHSkinQuality202000401 | Start Date*: 2021-04-30 |
| Sponsor Name:Prof. Dr. Martina Kerscher, University of Hamburg | ||
| Full Title: Skin perception after intradermal application of IncobotulinumtoxinA within upper and midface (Interventional Phase II) | ||
| Medical condition: Skin perception after intradermal application of INCOBOTULINUMTOXIN A within upper and midface | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| 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: 2009-016641-26 | Sponsor Protocol Number: 2009-01-QST | Start Date*: 2010-09-27 |
| Sponsor Name:ZARI - Univeristätsmedizin Göttingen | ||
| Full Title: The influence of propofol and inhalational anesthetics on postoperative pain perception | ||
| Medical condition: ISensory and pain perception in the skin of patients who receive anesthesia with two different anesthetics for elective surgery will be analyzed. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-004227-31 | Sponsor Protocol Number: 1312/BP | Start Date*: 2016-06-10 |
| Sponsor Name:OA Dr. Philipp Becker c/o Abteilung für Wirbelsäulenchirurgie, Orthopädisches Spital Speising GmbH | ||
| Full Title: Clinical pilot study to review the impact of perioperative administration of the synthetic cannabinoid nabilone in the context of spinal fusion surgery on the coping with surgery and the pain perce... | ||
| Medical condition: Spine disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-003821-31 | Sponsor Protocol Number: Futurum-963747 | Start Date*: 2022-03-15 |
| Sponsor Name:Region Jönköping, Sweden [...] | ||
| Full Title: Patient-controlled Sedation in Port Implantation (PACSPI 2)- a randomized controlled trial | ||
| Medical condition: Patients ≥18 years with cancer in need of subcutaneous venous port will be offered to participate in the trial. The aim of the trial is to determine if patient-controlled sedation (PCS) with prop... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-022472-31 | Sponsor Protocol Number: Lidocaine1 | Start Date*: 2010-12-23 |
| Sponsor Name:University Hospital of South Manchester | ||
| Full Title: The effect of Lidocaine and its Delivery in Patients with Chronic Cough | ||
| Medical condition: Chronic Cough | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-003514-39 | Sponsor Protocol Number: GNCbumet | Start Date*: Information not available in EudraCT |
| Sponsor Name:Gillberg Neuropsychiatry Centre | ||
| Full Title: Testing E/I imbalance in autism with Bumetanide – a parallel group randomized waitlist-control trial in adolescents and adults | ||
| Medical condition: Autism Spectrum Disorder | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-002002-46 | Sponsor Protocol Number: 2012-BMP1-2 | Start Date*: 2013-05-07 | |||||||||||
| Sponsor Name:Universitätsklinik für Zahn-, Mund- und Kieferheilkunde, Med Uni Graz, Department für zahnärztliche Chirurgie | |||||||||||||
| Full Title: A phase III, randomized, controlled clinical pilot trial of lateral ridge augmentation using autogenous bone blocks or xenogenic bone block grafts loaded with recombinant human bone morphogenic pro... | |||||||||||||
| Medical condition: Difference of percepetion/acceptance in patients trated with autogonous bone blocks or xenogenic bone block loaded with BMP2 to create a sufficent bonesituation Difference in quantity and quality... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-003641-95 | Sponsor Protocol Number: SELECTI-CARFAP | Start Date*: 2015-02-13 | |||||||||||
| Sponsor Name:Nicasio Pérez Castellano | |||||||||||||
| Full Title: Randomized clinical trial to study effective pharmacological cardioversion of paroxysmal atrial fibrillation by blocking ionic currents atrioselectivas by treatment with vernakalant vs Flecainide | |||||||||||||
| Medical condition: Atrial fibrillation paroxysmal | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-000805-22 | Sponsor Protocol Number: A20175CI03 | Start Date*: 2021-09-28 |
| Sponsor Name:Neuroplast BV | ||
| Full Title: A multi-center, double-blind, randomized, placebo-controlled, delayed- start phase II/III study to assess the efficacy and safety of Neuro-Cells in (sub)acute spinal cord injury patients | ||
| Medical condition: Traumatic Spinal cord injury | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-001920-31 | Sponsor Protocol Number: DMID11-0069 | Start Date*: 2014-12-09 | ||||||||||||||||||||||||||
| Sponsor Name:University College London | ||||||||||||||||||||||||||||
| Full Title: A PHASE II RANDOMIZED AND CONTROLLED INVESTIGATION OF SIX WEEKS OF ORAL VALGANCICLOVIR THERAPY IN INFANTS AND CHILDREN WITH CONGENITAL CYTOMEGALOVIRUS INFECTION AND HEARING LOSS. | ||||||||||||||||||||||||||||
| Medical condition: Children born with congenital CMV infection may develop sequelae on follow-up, particularly sensorineural hearing loss. A recent systematic review reports that 13.5% of babies with congenital CMV ... | ||||||||||||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2008-000132-40 | Sponsor Protocol Number: AM-111-CL-08-01 | Start Date*: 2008-11-18 | |||||||||||
| Sponsor Name:Auris Medical AG | |||||||||||||
| Full Title: Efficacy of AM 111 in Patients with Acute Sensorineural Hearing Loss: A Multi-Centre, Double-Blind, Randomised, Placebo-Controlled, Dose-Escalation Phase II Study | |||||||||||||
| Medical condition: Acute sensorineural hearing loss (ASNHL), which may be triggered by acoustic trauma, middle or inner ear surgery, i.e. known or evident insults to the inner ear. ASNHL may also result from a variet... | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) CZ (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) | ||
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