- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
8 result(s) found for: Subarachnoid space.
Displaying page 1 of 1.
| EudraCT Number: 2015-005033-53 | Sponsor Protocol Number: EG-01-1962-03 | Start Date*: 2017-02-01 | ||||||||||||||||
| Sponsor Name:Edge Therapeutics, Inc | ||||||||||||||||||
| Full Title: Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Efficacy and Safety Study Comparing EG-1962 to Standard of Care Oral Nimodipine in Adults with Aneurysmal Subarac... | ||||||||||||||||||
| Medical condition: Aneurysmal subarachnoid hemorrhage (aSAH) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) CZ (Completed) FI (Prematurely Ended) DK (Prematurely Ended) AT (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2014-003284-38 | Sponsor Protocol Number: EVG001SAH | Start Date*: 2016-02-15 | |||||||||||
| Sponsor Name:Evgen Pharma plc | |||||||||||||
| Full Title: SFX-01 AFTER SUBARACHNOID HAEMORRHAGE | |||||||||||||
| Medical condition: Subarachnoid Haemorrhage | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000241-39 | Sponsor Protocol Number: ID-054-304 | Start Date*: 2018-08-27 | ||||||||||||||||
| Sponsor Name:Idorsia Pharmaceuticals Ltd | ||||||||||||||||||
| Full Title: A prospective, multi-center, double-blind, randomized, placebo-controlled, parallel-group, Phase 3 study to assess the efficacy and safety of clazosentan in preventing clinical deterioration due to... | ||||||||||||||||||
| Medical condition: Aneurysmal Subarachnoid Hemorrhage | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FI (Completed) DE (Completed) SE (Completed) FR (Completed) CZ (Completed) BE (Completed) DK (Completed) HU (Completed) AT (Completed) PL (Completed) ES (Completed) IT (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: 2015-002383-16 | Sponsor Protocol Number: CME-LEM4 | Start Date*: 2016-01-19 |
| Sponsor Name:Fundación Investigación Biomédica Hospital Universitario Puerta de Hierro | ||
| Full Title: Evaluate the efficacy of the cell therapy with NC1 medication in patients with post-traumatic syringomyelia | ||
| Medical condition: Traumatic spinal cord injury, chronically established, associated with syringomyelia and neurological deficit 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: 2017-001824-23 | Sponsor Protocol Number: CME-LEC1 | Start Date*: 2017-11-29 |
| Sponsor Name:Fundación de Investigación Biomédica del Hospital Universitario Puerta de Hierro-Majadahonda (FIBM-HUPHM) | ||
| Full Title: Intrathecal administration of autologous adult bone marrow mesenchymal stem cells expanded in the diffuse axonal injury. | ||
| Medical condition: Traumatic cerebral injury, chronically established attributed to diffuse axonal injury. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-004132-22 | Sponsor Protocol Number: NPH-01 | Start Date*: 2021-01-20 | |||||||||||
| Sponsor Name:Uppsala University Hospital | |||||||||||||
| Full Title: Double-blind randomized acetazolamide trial in normal pressure hydrocephalus | |||||||||||||
| Medical condition: Normal pressure hydrocephalus | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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Query did not match any studies.