- Trials with a EudraCT protocol (9)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
9 result(s) found for: Broken neck.
Displaying page 1 of 1.
EudraCT Number: 2009-013462-25 | Sponsor Protocol Number: MW001 | Start Date*: 2009-09-28 | |||||||||||
Sponsor Name:NHS Greater Glasgow and Clyde Health Board | |||||||||||||
Full Title: A dose finding study for ultrasound guided anterior psoas compartment blocks in patients with a fractured neck of femur | |||||||||||||
Medical condition: Proximal traumatic fractured neck of femur | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001857-22 | Sponsor Protocol Number: Methadone-010922 | Start Date*: 2022-09-06 | |||||||||||||||||||||||||||||||
Sponsor Name:Sygehus Sønderjylland, Orthopedic department | |||||||||||||||||||||||||||||||||
Full Title: Perioperative Methadone for ameliorating postoperative pain and reduction in postoperative opioid consumption in hip fracture patients – Dosage adjusting pilot-study | |||||||||||||||||||||||||||||||||
Medical condition: Hip fractures | |||||||||||||||||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-001543-13 | Sponsor Protocol Number: HIP-SAP | Start Date*: 2018-03-28 | ||||||||||||||||||||||||||
Sponsor Name:Morten Tange Kristensen/Hvidovre Hospital | ||||||||||||||||||||||||||||
Full Title: Preliminary effect and safety of physiotherapy with strength training and protein-dense nutritional supplement in combination with anabolic steroids in cross-continuum rehabilitation of patients wi... | ||||||||||||||||||||||||||||
Medical condition: Area of investigation is recovery of muscle strength and function following hip fracture surgery. | ||||||||||||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-003875-77 | Sponsor Protocol Number: 1870 | Start Date*: 2018-01-24 | |||||||||||
Sponsor Name:University Hospitals of North Midlands NHS Trust | |||||||||||||
Full Title: A Randomised, Controlled Double Blinded Non-inferiority Trial of intravenous Morphine compared with intravenous Paracetamol for pain relief in patients presenting to the Emergency Department with S... | |||||||||||||
Medical condition: Fractured Neck of Femur | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002170-36 | Sponsor Protocol Number: 2014-002170-36 | Start Date*: 2015-02-11 |
Sponsor Name:Karolinska University Hospital | ||
Full Title: Treatment of Cervical Spinal Cord Injury with Imatinib – a safety and feasibility study | ||
Medical condition: Cervical Spinal Cord Injury | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001832-34 | Sponsor Protocol Number: 3100N7-211-WW | Start Date*: 2007-01-11 | |||||||||||
Sponsor Name:Wyeth Pharmaceuticals Inc. | |||||||||||||
Full Title: A Phase 2, Multicenter, Single-Blind, Randomized, Stratified, Standard-of-Care Controlled, Feasibility and Safety Study of rhBMP-2/CPM as an Adjuvant Therapy for Fractures of the Proximal Femur | |||||||||||||
Medical condition: Closed fracture of the proximal femur | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FI (Completed) HU (Completed) FR (Completed) SE (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000428-36 | Sponsor Protocol Number: ADJUNCT-1-2021 | Start Date*: 2021-04-21 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Zealand University Hospital, Department of Anaesthesiology | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Oral dexamethasone as an adjunct to a brachial plexus block in patients undergoing orthopaedic surgery of the forearm and hand. A randomised, blinded, placebo-controlled, parallel, triple-arm clini... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Participants undergoing surgery of the bones in the hand or forearm with a lateral infraclavicular brachial plexus block as the means of providing anaesthesia and analgesia will be investigated. We... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-023871-25 | Sponsor Protocol Number: 2010-023871-25 | Start Date*: 2011-04-20 | |||||||||||||||||||||
Sponsor Name:Nottingham University Hospitals NHS Trust | |||||||||||||||||||||||
Full Title: The FINOF(Femoral Nerve-Block Intervention in Neck Of Femur Fracture) Study | |||||||||||||||||||||||
Medical condition: Pain and mobility following hip fracture in the elderly | |||||||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-000654-38 | Sponsor Protocol Number: AHUS2015-000654-38 | Start Date*: 2015-10-19 | |||||||||||
Sponsor Name:Akershus University Hospital, Norway | |||||||||||||
Full Title: Secondary prophylaxis after hip fracture. An evaluation og two organisational models based on choise of treatment: a comparison of efficacy and applicability of hospital based treatment with zoled... | |||||||||||||
Medical condition: Hip fracture | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Prematurely Ended) | |||||||||||||
Trial results: View results |
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