- Trials with a EudraCT protocol (412)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
412 result(s) found for: Traumatic.
Displaying page 8 of 21.
EudraCT Number: 2005-000534-20 | Sponsor Protocol Number: THAM05 | Start Date*: 2005-03-15 |
Sponsor Name:Addenbrooke's Hospital NHS Foundation Trust | ||
Full Title: Influence of brain tissue pH regulation on cerebral oxygenation and metabolism in patients with severe traumatic brain injury. | ||
Medical condition: Severe traumatic brain injury | ||
Disease: | ||
Population Age: Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004250-15 | Sponsor Protocol Number: | Start Date*: 2018-06-08 | |||||||||||
Sponsor Name:University Hospitals Birmingham | |||||||||||||
Full Title: A prospective, phase II, single centre, cross-sectional, randomised trial investigating Dehydroepiandrosterone and it's Pharmacokinetics in Trauma | |||||||||||||
Medical condition: DHEA depletion in trauma and hip fracture patients. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000641-23 | Sponsor Protocol Number: CNWL/MC/AFT/01 | Start Date*: 2015-11-24 |
Sponsor Name:Central and North West London NHS Foundation Trust | ||
Full Title: Aggression Following TBI: Effectiveness of Risperidone (AFTER)-a feasibility RCT. | ||
Medical condition: aggression and agitation following on from a traumatic brain injury | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-000898-23 | Sponsor Protocol Number: 2019/KEP/218 | Start Date*: 2019-08-01 | |||||||||||
Sponsor Name:London School of Hygiene and Tropical Medicine | |||||||||||||
Full Title: Pharmacokinetics of intramuscular tranexamic acid in trauma patients: a clinical trial | |||||||||||||
Medical condition: Traumatic haemorrhage | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005613-24 | Sponsor Protocol Number: CME-LEM3 | Start Date*: 2015-06-19 |
Sponsor Name:Fundación Investigación Biomédica Hospital Universitario Puerta de Hierro | ||
Full Title: Intrathecal administration (pattern 100/3) of expanded autologous adult bone marrow mesenchymal troncal cells in established chronic spinal cord injuries | ||
Medical condition: Traumatic or ischemic spinal cord injury, chronically established and considered irreversible | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-000975-10 | Sponsor Protocol Number: CME-LEM5 | Start Date*: 2017-09-25 |
Sponsor Name:Fundación Investigación Biomédica Hospital Universitario Puerta de Hierro Majadahonda | ||
Full Title: Intrathecal administration of bone marrow adult autologous stem mesenchymal cells expanded in chronically established low injuries of the spinal cord | ||
Medical condition: Traumatic or ischemic spinal cord injury, chronically established and considered irreversible | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-005684-24 | Sponsor Protocol Number: CME-LEM2 | Start Date*: 2014-01-16 | |||||||||||
Sponsor Name:Fundación Investigación Biomédica Hospital Universitario Puerta de Hierro | |||||||||||||
Full Title: Subarachnoid administration of autologous bone marrow stromal cells in incomplete spinal cord injury. | |||||||||||||
Medical condition: Incomplete spinal cord injury, due to traumatical or ischemic cause. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004812-81 | Sponsor Protocol Number: 2019-48 | Start Date*: 2021-03-05 |
Sponsor Name:ASSISTANCE PUBLIQUE HOPITAUX DE MARSEILLE | ||
Full Title: Ketamine Low dOse Evaluation on morphine consumption in traumatic patient : a prospective randomized controlled double-blind study | ||
Medical condition: Traumatism | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002569-37 | Sponsor Protocol Number: APHP180584 | Start Date*: 2020-05-13 |
Sponsor Name:Assistance Publique Hôpitaux de Paris | ||
Full Title: Empirical steroids and/or antifungals in immunocompromised patients with acute respiratory failure from undetermined etiology: a multicenter double-blind randomized controlled trial | ||
Medical condition: immunocompromised patients with acute respiratory failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2022-001777-31 | Sponsor Protocol Number: IG2021370 | Start Date*: 2023-05-08 |
Sponsor Name:Hospital de Neurorrehabilitación Institut Guttmann | ||
Full Title: Pilot study on the effect of cannabinoids THC + CBD on resistant spasticity in patients with chronic spinal cord injury. | ||
Medical condition: Pilot study on the effect of THC+CBD cannabinoids on resistant spasticity in patients with chronic spinal cord injury. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023888-17 | Sponsor Protocol Number: OMS103-MEN-003 | Start Date*: 2011-05-11 | |||||||||||
Sponsor Name:Omeros Corporation | |||||||||||||
Full Title: A Randomized, Double-Blind, Parallel Group, Vehicle-Controlled Study to Evaluate the Safety and Efficacy of OMS103HP-S Administered in Joint Irrigation Solution to Subjects Undergoing Arthroscopic ... | |||||||||||||
Medical condition: Arthroscopic surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003891-20 | Sponsor Protocol Number: NL17389.091.07 | Start Date*: 2007-11-27 | |||||||||||
Sponsor Name:GGZ Nijmegen | |||||||||||||
Full Title: Een gerandomiseerde placebo gecontroleerde studie naar de toegevoegde waarde van D-cycloserine aan exposure therapie bij patiënten met een poststraumatische stress stoornis | |||||||||||||
Medical condition: Posttraumatic stress disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000030-39 | Sponsor Protocol Number: na | Start Date*: 2008-12-16 |
Sponsor Name:Ministery of Defense, Military Mental Health - Research Centre | ||
Full Title: Prazosin as add-on therapy in the pharmacological treatment of sleep disturbances in post traumatic stress disorder, a placebo-controlled study using polysomnography | ||
Medical condition: posttraumatic stress disorder (PTSD) | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000223-42 | Sponsor Protocol Number: ZiSe | Start Date*: 2005-10-31 |
Sponsor Name:University Hospital Hamburg-Eppendorf, Psychiatry | ||
Full Title: Effects of ziprasidone vs. placebo during the first four weeks of eight weeks sertraline treatment in patients with posttraumatic stress disorder (PTSD) | ||
Medical condition: Post-traumatic Stress Disorder (PTSD) according to DSM-IV criteria | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-004669-24 | Sponsor Protocol Number: 8103 | Start Date*: 2009-01-02 |
Sponsor Name:Research Innovation Services, University of Nottingham | ||
Full Title: Nitrous Oxide and Cerebral Autoregulation | ||
Medical condition: This study is being conducted to evaluate the effects of inhaled concentrations of 20%, 30% and 40% Nitrous Oxide on cerebral autoregulation in healthy volunteers using transcranial doppler ultraso... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-001353-41 | Sponsor Protocol Number: NL56714.029.16 | Start Date*: 2016-06-06 |
Sponsor Name:VU University medical center Amsterdam | ||
Full Title: Oxygenation of Affected Limbs in CRPS-I Patients | ||
Medical condition: Complex Regional Pain Syndrome, Neuropathic Pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003197-57 | Sponsor Protocol Number: A0081181 | Start Date*: 2012-11-09 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Pfizer Worldwide Research and Development | ||||||||||||||||||||||||||||||||||||||
Full Title: A MULTIPLE DOSE PHARMACOKINETIC OPEN-LABEL STUDY OF PREGABALIN (LYRICA) IN HEALTHY LACTATING WOMEN | ||||||||||||||||||||||||||||||||||||||
Medical condition: neuropathic pain associated with diabetic peripheral neuropathy postherpetic neuralgia neuropathic pain related to spinal cord injury (US), fibromyalgia (US, JP) treatment of central and periphe... | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
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: 2011-001650-29 | Sponsor Protocol Number: MF02/11 | Start Date*: 2011-12-19 |
Sponsor Name:A. Carlsson Research AB | ||
Full Title: TREATMENT OF MENTAL FATIGUE ("BRAIN FATIGUE") WITH THE DOPAMINERGIC STABILIZER OSU6162 AFTER STROKE AND MILD/MODERATE TRAUMATIC BRAIN INJURY– INCREASE OF PATIENT NUMBER | ||
Medical condition: Mental fatigue after stroke or mild to moderate head trauma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004373-80 | Sponsor Protocol Number: ASBI603 | Start Date*: 2013-06-21 | |||||||||||
Sponsor Name:Asubio Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of SUN13837 Injection in Adult Subjects with Acute Spinal Co... | |||||||||||||
Medical condition: Acute spinal cord injury | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) CZ (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
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