- Trials with a EudraCT protocol (85)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (5)
85 result(s) found for: Pathophysiology.
Displaying page 1 of 5.
| EudraCT Number: 2011-000626-29 | Sponsor Protocol Number: KS001 | Start Date*: 2011-12-13 |
| Sponsor Name:QUEEN MARY UNIVERSITY OF LONDON | ||
| Full Title: Keloid Scars: A randomised clinical and laboratory based study on the treatment and differentiation factors of the local disease | ||
| Medical condition: Keloid scarring | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-003617-33 | Sponsor Protocol Number: 03-2005 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Charité | ||
| Full Title: A Randomised Cross-Over Study to Explore the Pathophysiological Mechanisms Involved in the Treatment of Actinic Keratoses with Solaraze | ||
| Medical condition: actinic keratosis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-001384-12 | Sponsor Protocol Number: PancolonicPressurization | Start Date*: 2014-07-16 |
| Sponsor Name:KULEUVEN | ||
| Full Title: IS THE ABSENCE OF PAN-COLONIC PRESSURIZATIONS A RELEVANT PATHOPHYSIOLOGICAL MECHANISM IN A SUBGROUP OF PATIENTS WITH CHRONIC IDIOPHATIC CONSTIPATION? | ||
| Medical condition: COLONIC MOTILITY WILL BE STUDIED BOTH IN HEALTHY SUBJECTS AND IN PATIENTS WITH CHRONIC CONSTIPATION | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-003022-89 | Sponsor Protocol Number: 1.1 | Start Date*: 2019-10-18 | |||||||||||
| Sponsor Name:HELLENIC INSTITUTE FOR THE STUDY OF SEPSIS | |||||||||||||
| Full Title: GUT-DERIVED INCRETIN HORMONES IN THE PATHOPHYSIOLOGY OF TYPE 1 DIABETES MELLITUS; EFFECT OF METFORMIN TREATMENT (THE INCREDIBLE-ME TRIAL) | |||||||||||||
| Medical condition: GUT-DERIVED INCRETIN HORMONES IN THE PATHOPHYSIOLOGY OF TYPE 1 DIABETES MELLITUS; EFFECT OF METFORMIN TREATMENT | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-000197-35 | Sponsor Protocol Number: IR-HP-14-01 | Start Date*: 2015-06-09 | ||||||||||||||||
| Sponsor Name:AOU DI BOLOGNA POLICLINICO S.ORSOLA-MALPIGHI | ||||||||||||||||||
| Full Title: insulin resistance, obesity and gastrointestinal bacteria | ||||||||||||||||||
| Medical condition: Helicobacter pylori infection | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-004115-27 | Sponsor Protocol Number: IIBSP-OXI-2020-102 | Start Date*: 2021-05-10 |
| Sponsor Name:Institut de Recerca Hospital de la Santa Creu i Sant Pau - IIB Sant Pau | ||
| Full Title: Identification and clinical relevance of oxytocin deficient status: randomized, crossover, placebo-controlled pathophysiological pilot study: GLP1 study | ||
| Medical condition: Hypopituitarism | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-000396-20 | Sponsor Protocol Number: Dropizol_2020 | Start Date*: 2021-01-02 | |||||||||||
| Sponsor Name:Mech-Sense, Aalborg University Hospital | |||||||||||||
| Full Title: Opium tincture against chronic diarrhea - Patients: An investigator initiated, randomized placebo-controlled, clinical trial | |||||||||||||
| Medical condition: Chronic diarrhea | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-003116-22 | Sponsor Protocol Number: RBK091 | Start Date*: 2006-12-21 |
| Sponsor Name:Prof. Sechtem, Department of Cardiology, Robert Bosch Hospital | ||
| Full Title: Application of Sildenafil in patients with documented coronary vasospasm in order to explore the pathophysiology of coronary vasospasm and the therapeutic effects of Sildenafil in patients sufferin... | ||
| Medical condition: Coronary vasospasm is an abrupt severe vasoconstriction of coronary arteries leading to myocardial ischemia and angina pectoris. The reason for the occurrence of coronary spasm and the cellular mec... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-019891-54 | Sponsor Protocol Number: WC2010-022 | Start Date*: 2010-08-10 |
| Sponsor Name:VU University Medical Center | ||
| Full Title: Effects of oral corticosteroids and DMSO on inflammatory signs and symptoms in Complex Regional Pain Syndrome type 1 | ||
| Medical condition: Complex regional pain syndrome type 1. This condition is a pain syndrome with unknown pathophysiology. Research shows that inflammation plays a role in the development and course of the disease. Ev... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-016924-30 | Sponsor Protocol Number: NorCAPITAL | Start Date*: Information not available in EudraCT |
| Sponsor Name:Division of Paediatrics, Rikshospitalet University Hospital | ||
| Full Title: NorCAPITAL The Norwegian Study of Chronic Fatigue Syndrome in Adolescents: Pathophysiology and Intervention Trial | ||
| Medical condition: Chronic fatigue syndrom/myalgic encephalomyelitis (CFS/ME) in adolescents | ||
| Disease: | ||
| Population Age: Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: NO (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-000746-32 | Sponsor Protocol Number: 5-HT_CFM | Start Date*: 2008-04-23 |
| Sponsor Name:Karolinska Institutet | ||
| Full Title: Validation of experimental pain models as translational for craniofacial myalgia with respect to the influence of 5-HT, glutamate, cortisol and estradiol level | ||
| Medical condition: Patients with craniomandibular myalgia (CM), i.e. with pain in the masster muscle and a diagnosis of myofascial pain according to the RDC/TMD criteria, and healthy subjects of both sexes, over 18 y... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-004629-18 | Sponsor Protocol Number: helmich-veni-2019 | Start Date*: 2017-04-13 |
| Sponsor Name:Radboud University Nijmegen | ||
| Full Title: The noradrenergic basis of Parkinson’s tremor: a systems-level fMRI approach | ||
| Medical condition: Tremor in Parkinson's disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-002567-24 | Sponsor Protocol Number: M120204-063 | Start Date*: 2005-04-04 |
| Sponsor Name:Millennium Pharmaceuticals, Inc. | ||
| Full Title: A Phase 2a Magnetic Resonance Imaging Study of the Safety and Efficacy of MLN1202 in patients with Multiple Sclerosis | ||
| Medical condition: The purpose of this study is to investigate the safety, PK parameters, PD responses, and clinical responses of multiple dose administration of MLN1202 in patients with relapsing remitting multiple ... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Completed) GB (Completed) HU (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-001176-30 | Sponsor Protocol Number: 20167169 | Start Date*: 2016-06-15 |
| Sponsor Name:Clinical Research Institute, HUCH Ltd. | ||
| Full Title: Effects of PCSK9 inhibition by Evolocumab on postprandial lipid metabolism in type 2 diabetes | ||
| Medical condition: type 2 diabetes | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-002970-36 | Sponsor Protocol Number: 54508 | Start Date*: 2016-06-06 |
| Sponsor Name:Maastricht University Medical Center | ||
| Full Title: Human intestinal ischemia and reperfusion | ||
| Medical condition: The participants enrolled in this study will all undergo major upper abdominal surgery (i.e. mostly Pylorus Preserving Pancreatico Duodenectomy or whipple procedure) mostly for pancreatic cancer, p... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-001611-20 | Sponsor Protocol Number: 357-0-0 | Start Date*: 2018-07-24 |
| Sponsor Name:University of Tübingen | ||
| Full Title: Pathophysiology-based therapy of epileptic encephalopathies | ||
| Medical condition: patients with epileptic encephalopathies | ||
| Disease: | ||
| Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-002007-97 | Sponsor Protocol Number: 2017/24JUL/374 | Start Date*: 2017-12-07 |
| Sponsor Name:Cliniques universitaires Saint-Luc | ||
| Full Title: Does LOW Dose DEXmedetomidine After Cardiopulmonary Bypass Separation Decrease the Incidence of DELirium: A Double-blind Randomized Placebocontrolled Study (LOWDEXDEL Study) | ||
| Medical condition: To find if Dexmedetomidine in cardiac surgery would have any neuroprotective effects by stimulating the alpha 2A-receptors and as such would decrease the incidence of postoperative delirium. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-002634-20 | Sponsor Protocol Number: NBF_HK_01_2018 | Start Date*: 2018-10-23 | ||||||||||||||||
| Sponsor Name:Anaesthesia Department, Hvidovre Hospital, Capital Region of Denmark | ||||||||||||||||||
| Full Title: Highdose steroid for total knee arthroplasty - A randomized doubleblindet controlled trial. | ||||||||||||||||||
| Medical condition: Perioperative management of total knee-arthroplasty because of knee-osteoarthritis | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2018-002636-25 | Sponsor Protocol Number: NBF_HK_03_2018 | Start Date*: 2018-10-23 | |||||||||||||||||||||
| Sponsor Name:Anaesthesia Department, Hvidovre Hospital, Capital Region of Denmark. | |||||||||||||||||||||||
| Full Title: Highdose Steroid for High Pain Responders undergoing Total Hip-arthroplasty - A randomized doubleblindet controlled trial. | |||||||||||||||||||||||
| Medical condition: Perioperative management of total hip-arthroplasty because of hip-osteoarthritis | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2018-003286-34 | Sponsor Protocol Number: CHUBX2017/22 | Start Date*: 2019-03-05 | ||||||||||||||||
| Sponsor Name:CHU de Bordeaux | ||||||||||||||||||
| Full Title: In vivo involvement of the cholinergic and dopaminergic systems in the pathophysiology of apathy. | ||||||||||||||||||
| Medical condition: Apathy | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
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