- Trials with a EudraCT protocol (10)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
10 result(s) found for: Excision repair.
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EudraCT Number: 2022-000077-57 | Sponsor Protocol Number: 2021-THORANE-Pharma-001 | Start Date*: 2022-06-25 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Rigshospitalet | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Methadone versus fentanil and oxycodone for post-operative pain reduction in patients undergoing coronary artery bypass grafting and/or valve surgery – a placebo-controlled, double-blind, randomiz... | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: We investigate the efficacy of methadonehydrochloride for reducing optoperative opioid requirements, pain scores and improving quality of recovery in patients undergoing heart surgery (i.e. corona... | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002344-99 | Sponsor Protocol Number: SKY0402-C-203 | Start Date*: 2005-03-03 | |||||||||||
Sponsor Name:SkyePharma, Inc. | |||||||||||||
Full Title: A Phase 2, Multicenter, Randomized, Double-Blind, Dose-Escalating/De-Escalating Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of Sustained-Release Encapsulated Bupivacaine (SKY0402) ... | |||||||||||||
Medical condition: Pain following bunionectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004237-21 | Sponsor Protocol Number: Metamizole003 | Start Date*: 2020-11-27 |
Sponsor Name:Jessa Hospital | ||
Full Title: Evaluation of the added value of Metamizole to standard postoperative treatment after ambulant shoulder surgery: a double-blind, randomized controlled trial | ||
Medical condition: Optimalisation of postoperative treatment after ambulant shoulder arthroscopy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001672-70 | Sponsor Protocol Number: 17.3.2008 | Start Date*: 2008-05-30 | ||||||||||||||||
Sponsor Name:Heli Leppikangas | ||||||||||||||||||
Full Title: The effects of levosimendan on haemodynamics in patients undergoing elective aortic valve replacement (AVR) together with coronary artery bypass grafting (CABG) surgry | ||||||||||||||||||
Medical condition: Aortic valve dysfunction and coronary artery disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-001777-33 | Sponsor Protocol Number: EARTH-TAVR01 | Start Date*: 2016-09-01 | |||||||||||
Sponsor Name:Charité Universitätsmedizin Berlin | |||||||||||||
Full Title: EVALUATION OF CEREBRAL THROMBOEMBOLISM AFTER TAVR | |||||||||||||
Medical condition: Patients with severe aortic stenosis that require Transcatheter aortic valve replacement are at risk for stroke. This study is to evaluate the occurrence and extent of cerebral embolization (total... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002801-23 | Sponsor Protocol Number: Metamizole002 | Start Date*: 2019-10-08 |
Sponsor Name:Jessa Hospital | ||
Full Title: Evaluation of the added value of Metamizole to standard post-operative treatment after ambulant surgery: a double-blind, randomized controlled trial | ||
Medical condition: Optimalization of post-operative treatment after ambulant surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000632-26 | Sponsor Protocol Number: TMC-BIV-11-02 | Start Date*: 2013-03-22 | |||||||||||
Sponsor Name:The Medicines Company | |||||||||||||
Full Title: Effect of Bivalirudin on Aortic Valve Intervention Outcomes 2/3 | |||||||||||||
Medical condition: Patients undergoing transcatheter aortic valve replacement (TAVR) procedures performed via the transfemoral approach. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) NL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004939-38 | Sponsor Protocol Number: IFCT-0801 | Start Date*: 2008-10-16 | ||||||||||||||||
Sponsor Name:IFCT | ||||||||||||||||||
Full Title: Essai randomisé de phase II/III évaluant une stratégie thérapeutique post-opératoire individualisée chez les patients opérés d’un carcinome bronchique non à petites cellules (CBNPC) non épidermoïde... | ||||||||||||||||||
Medical condition: L’hypothèse scientifique est que l’utilisation de marqueurs biologiques permettra d’optimiser le traitement adjuvant chez les patients opérés d’un cancer bronchique non à petites cellules. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-001975-30 | Sponsor Protocol Number: BAY59-7939/17938 | Start Date*: 2016-01-12 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: Global multicenter, open-label, randomized, event-driven, active-controlled study comparing a rivAroxaban-based antithrombotic strategy to an antipLatelet-based strategy after transcatheter aortIc ... | |||||||||||||
Medical condition: Patients with severe aortic stenosis that require Transcatheter aortic valve replacement are at risk of thrombus formation. Rivaroxaban (oral-anticoagulant) may reduce this risk, without increasing... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Prematurely Ended) BE (Prematurely Ended) NO (Prematurely Ended) AT (Prematurely Ended) DK (Prematurely Ended) SE (Prematurely Ended) NL (Prematurely Ended) GB (Prematurely Ended) FR (Prematurely Ended) CZ (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001764-36 | Sponsor Protocol Number: ITACA | Start Date*: 2008-08-13 | |||||||||||
Sponsor Name:Azienda Ospedaliero Universitaria ''San Luigi Gonzaga'' | |||||||||||||
Full Title: Phase III Multicenter Randomized Trial Comparing Adjuvant Pharmacogenomic-Driven Chemotherapy versus Standard Adjuvant Chemotherapy in Completely Resected Stage II-IIIA Non-Small Cell Lung Cancer. | |||||||||||||
Medical condition: patients with completely resected Stage II-IIIA non-small cell lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
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