- Trials with a EudraCT protocol (133)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
133 result(s) found for: Impact of Event Scale - Revised.
Displaying page 1 of 7.
| EudraCT Number: 2017-002456-88 | Sponsor Protocol Number: Stroke34 | Start Date*: 2023-02-28 | |||||||||||
| Sponsor Name:CENTRO HOSPITALAR E UNIVERSITÁRIO DE COIMBRA, E.P.E | |||||||||||||
| Full Title: STROKE34: randomized controlled phase IIa trial of intra-arterial CD34+ cells in acute ischemic stroke. | |||||||||||||
| Medical condition: Acute ischemic stroke | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004263-84 | Sponsor Protocol Number: CHUBX2017/29 | Start Date*: 2021-02-24 |
| Sponsor Name:CHU de Bordeaux | ||
| Full Title: AntiPlatelet theraPy stratEgy followiNg left atrial appenDAGe closurE | ||
| Medical condition: Atrial Fibrillation, atrial appendage, anticoagulants, stroke, platelet aggregation inhibitors | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-000095-10 | Sponsor Protocol Number: 69HCL18_0235 | Start Date*: 2021-07-20 | |||||||||||
| Sponsor Name:Hospices Civils de Lyon | |||||||||||||
| Full Title: Evaluation of the long-term efficacy of the injection of botulinum toxin A into the salivary glands versus scopolamine patches in the treatment of drooling in children over 4 years old with cerebra... | |||||||||||||
| Medical condition: Children with cerebral palsy aged 4 years old and over, presenting a pathological drooling | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-003833-14 | Sponsor Protocol Number: GOIRC-05-2018 | Start Date*: 2019-03-21 | ||||||||||||||||
| Sponsor Name:GRUPPO ONCOLOGICO ITALIANO DI RICERCA CLINICA (GOIRC) | ||||||||||||||||||
| Full Title: A Phase IV study on impact of Edoxaban treatment in Italian cancer patients with venous thromboembolism (EDOI Cancer Study) during antineoplastic therapy | ||||||||||||||||||
| Medical condition: Venous thromboembolism event associated with cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2016-003888-19 | Sponsor Protocol Number: OSU6162DB003 | Start Date*: 2017-03-20 |
| Sponsor Name:A. Carlsson Research AB | ||
| Full Title: Double-blind, randomised, placebo-controlled study to evaluate the efficacy and safety of OSU6162 in the treatment of residual symptoms after stroke | ||
| Medical condition: Stroke | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-001054-96 | Sponsor Protocol Number: 000013/BT | Start Date*: 2020-03-19 | |||||||||||
| Sponsor Name:Bone Therapeutics S.A. | |||||||||||||
| Full Title: Phase IIb, Placebo-Controlled, Randomized, Double-blind, Multicenter Study to Assess the Efficacy and Safety of Allogeneic Osteoblastic Cells (ALLOB) Single Implantation in Tibial Fracture | |||||||||||||
| Medical condition: Tibial fracture considered at risk of DU/NU (based on the combination of risk factors documented to be associated with increased proportion of DU/NU). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) FR (Completed) DE (Prematurely Ended) HU (Prematurely Ended) PL (Prematurely Ended) ES (Ongoing) CZ (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-003646-33 | Sponsor Protocol Number: 20190008 | Start Date*: 2020-06-24 | |||||||||||
| Sponsor Name:Amgen, Inc. | |||||||||||||
| Full Title: Comprehensive Assessment of Erenumab Efficacy in Subjects With High Frequency Episodic Migraine With at Least 1 Previously Failed Preventive Treatment: a Global, Double-blind, Placebo-controlled Ph... | |||||||||||||
| Medical condition: High frequency episodic migraine | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) PT (Completed) HU (Completed) BG (Completed) CZ (Completed) IT (Completed) RO (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-000312-36 | Sponsor Protocol Number: PTSD-FMS | Start Date*: 2021-05-19 | ||||||||||||||||
| Sponsor Name:Henri Laborit Hospital | ||||||||||||||||||
| Full Title: Impact of Post-Traumatic Stress Disorder Treatment by Reconsolidation Therapy on Fibromyalgia Syndrome | ||||||||||||||||||
| Medical condition: Post-Traumatic Stress Disorder and fibromyalgia syndrome | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2007-004286-18 | Sponsor Protocol Number: HPA-PTSD-1 | Start Date*: 2008-08-05 |
| Sponsor Name:Central Institute of Mental Health | ||
| Full Title: Monocentric, Double-blind Placebo-Controlled, Randomized Cross-Sectional Clinical Trial of Hydrocortisone (10 and 30mg/d) in Outpatients with Posttraumatic-Stress- Disorder (PTSD) ... | ||
| Medical condition: Intrusions in patients with posttraumatic stress disorder | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-020886-26 | Sponsor Protocol Number: MRZ60201_3053_1 | Start Date*: 2011-12-15 | |||||||||||
| Sponsor Name:Merz Pharmaceuticals GmbH | |||||||||||||
| Full Title: Prospective, open-label, non-randomized, single-arm, multi-center dose titration study to investigate the safety and efficacy of NT 201 in subjects deemed to require total body doses of 800 U of NT... | |||||||||||||
| Medical condition: Spasticity of the upper and lower limb of the same body side due to cerebral causes | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Completed) PT (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-004191-22 | Sponsor Protocol Number: PH001Precycle | Start Date*: 2017-06-20 |
| Sponsor Name:Palleos healthcare GmbH | ||
| Full Title: PRECYCLE: Multicenter, randomized phase IV intergroup trial to evaluate the impact of e Health-based patient reported outcome (PRO) assessment on quality of life in patients with hormone receptor p... | ||
| Medical condition: advanced and or metastatic breast cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-000284-14 | Sponsor Protocol Number: | Start Date*: 2016-01-05 |
| Sponsor Name:University of Calgary | ||
| Full Title: Assessment of Metoprolol in the Prevention of Vasovagal Syncope in Aging Subjects | ||
| Medical condition: Vasovagal Syncope | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-003134-14 | Sponsor Protocol Number: PDY6045 | Start Date*: 2007-06-04 |
| Sponsor Name:Sanofi-aventis U.S. Inc. | ||
| Full Title: A randomized, multinational, double-blind, placebo-controlled, parallel-group design pilot study to estimate the tolerability, safety, pharmacokinetics, and pharmacodynamic effects of teriflunomide... | ||
| Medical condition: Multiple sclerosis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) IT (Completed) ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-004893-29 | Sponsor Protocol Number: PDY6046 | Start Date*: 2007-07-25 |
| Sponsor Name:Sanofi-aventis U.S. Inc. | ||
| Full Title: A randomized, multinational, double-blind, placebo-controlled, parallel-group design pilot study to estimate the tolerability, safety, pharmacokinetics, and pharmacodynamic effects of teriflunomide... | ||
| Medical condition: Multiple sclerosis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) DE (Completed) AT (Completed) IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-000756-17 | Sponsor Protocol Number: S61145 | Start Date*: 2018-05-30 | |||||||||||
| Sponsor Name:KU Leuven | |||||||||||||
| Full Title: Impact of Tight blood Glucose Control within normal fasting ranges with insulin titration prescribed by the Leuven algorithm in adult critically ill patients | |||||||||||||
| Medical condition: Hyperglycemia in critically ill patients (stress hyperglycemia) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-004456-42 | Sponsor Protocol Number: P2021/Anesth/MIDEXMRI | Start Date*: 2022-06-21 |
| Sponsor Name:Hôpital Universitaire Des Enfants Reine Fabiola | ||
| Full Title: Prospective, randomized, double-blind, double-dummy, active-controlled, phase 3 clinical trial comparing the safety and efficacy of intranasal dexmedetomidine to oral midazolam as premedication for... | ||
| Medical condition: pre-school pediatric population undergoing magnetic resonance imaging | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-004571-41 | Sponsor Protocol Number: RBMinCovid19 | Start Date*: 2021-02-23 | |||||||||||
| Sponsor Name:Cyxone AB | |||||||||||||
| Full Title: A Randomized, Placebo Controlled, Double Blind Study to Evaluate the Safety and Efficacy of Rabeximod Compared to Standard of Care in Patients With Moderate Coronavirus Disease (COVID-19) | |||||||||||||
| Medical condition: Coronavirus Disease (COVID-19) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) HU (Prematurely Ended) LV (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-006113-34 | Sponsor Protocol Number: XAMNPIOAP2011 | Start Date*: 2013-10-24 |
| Sponsor Name:AURORA PUJOL ONOFRE | ||
| Full Title: Effect of pioglitazone administred to patients with Adrenomyeloneuropathy: A phase II, Singlearm, Monocentric Trial. | ||
| Medical condition: X-linked adrenoleukodystrophy | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-001663-24 | Sponsor Protocol Number: INSIGHT012 | Start Date*: 2021-09-20 | |||||||||||
| Sponsor Name:Office of Sponsored Projects,University of Minnesota | |||||||||||||
| Full Title: An International Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial of the Safety and Efficacy of Anti-Coronavirus Hyperimmune Intravenous Immunoglobulin for the Treatment of Adult Out... | |||||||||||||
| Medical condition: We are investigating Coronavirus disease 2019 (COVID-19) which is predominantly a respiratory disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Trial now transitioned) DK (Trial now transitioned) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-018878-21 | Sponsor Protocol Number: SSAT036 | Start Date*: 2010-08-16 |
| Sponsor Name:St Stephen's AIDS Trust | ||
| Full Title: A phase III, open-label, single centre, single-arm, pilot study to assess the feasibility of switching, individuals receiving efavirenz with continuing Central Nervous System (CNS) toxicity, to ral... | ||
| Medical condition: HIV | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
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