- Trials with a EudraCT protocol (7)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
7 result(s) found for: ankle fusion.
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EudraCT Number: 2017-002185-51 | Sponsor Protocol Number: Poplitea2017 | Start Date*: 2017-10-18 | |||||||||||
Sponsor Name:Tampere University Hospital | |||||||||||||
Full Title: Effect of perineural dexamethasone on the duration of popliteal nerve block for analgesia after ankle surgery | |||||||||||||
Medical condition: Ankle arthrosis, situation after ankle injury or malposition of ankle/foot, arthrodesis as a curative therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000608-27 | Sponsor Protocol Number: ProtokolSB2 | Start Date*: 2016-04-05 | |||||||||||||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||||||||||||
Full Title: The effect of subsartorial saphenous block on postoperative pain following major ankle and hind foot surgery | |||||||||||||||||||||||
Medical condition: Post-operative pain after four types of major ankle and hind foot surgery: (1) total ankle arthroplasty, (2) ankle arthrodesis, (3) subtalar arthrodesis or (4) triple arthrodesis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-004207-78 | Sponsor Protocol Number: ProtokolSB1 | Start Date*: 2015-01-07 | |||||||||||||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||||||||||||
Full Title: Comparison of the effect of saphenous block with plain bupivacaine vs. protracted bupivacaine mixture as a supplement to continuos sciatic catheter after major ankle and foot surgery: a randomized ... | |||||||||||||||||||||||
Medical condition: Post-operative pain after three types of major ankle and hind foot surgery: (1) total ankle arthroplasty, (2) ankle arthrodesis or (3) subtalar arthrodesis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-004779-36 | Sponsor Protocol Number: BMTI-2006-03-EU | Start Date*: 2007-01-22 | |||||||||||
Sponsor Name:BioMimetic Therapeutic Inc | |||||||||||||
Full Title: A Human Clinical Trial to Evaluate the Safety and Clinical Utility of GEM OS1 as a Bone Regeneration System in Foot and Ankle Arthrodesis Procedures | |||||||||||||
Medical condition: For use as a bone void filler for voids or gaps that are not intrinsic to the stability of bony structure. Treatment of surgically created osseous defects or osseous defects resulting from patholo... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FR (Completed) AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000707-28 | Sponsor Protocol Number: FODANKEL01 | Start Date*: 2014-07-04 | ||||||||||||||||
Sponsor Name:Aarhus University Hospital | ||||||||||||||||||
Full Title: Displacement of popliteal sciatic nerve catheters after major foot and ankle surgery. Long axis (LAX) compared with short axis (SAX), a MR/US image fusion study | ||||||||||||||||||
Medical condition: The medical condition to be examined in this study, is postoperative pain after major foot and ankle surgery. Which way to insert a sciatic nerve catheter to treat postoperative pain is the most ef... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-021435-14 | Sponsor Protocol Number: n.a. | Start Date*: 2010-12-06 |
Sponsor Name:Academisch Medisch Centrum Amsterdam | ||
Full Title: Effects of abatacept (Orencia®) on biomarkers in synovial tissue in patients with rheumatoid arthritis | ||
Medical condition: rheumatoid arthritis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-003768-67 | Sponsor Protocol Number: IM101119 | Start Date*: 2007-03-23 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase III Multicenter, Randomized, Double-Blind, placebo-controlled Study to Assess short-term changes in synovitis and structural damage outcomes in subjects with active Rheumatoid Arthritis and... | |||||||||||||
Medical condition: RHEUMATOID ARTHRITIS,NOS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GB (Completed) DE (Completed) NL (Completed) BE (Completed) AT (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: Removed from public view |
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