- Trials with a EudraCT protocol (48)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
		
	   		
	   		    
                    
                   	
                   	    48 result(s) found for: Arthroscopy.
                    
                
			
   			
		
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	| EudraCT Number: 2022-000093-25 | Sponsor Protocol Number: 01_20012022 | Start Date*: 2022-05-05 | |||||||||||
| Sponsor Name:Aarhus University Hospital | |||||||||||||
| Full Title: The effect of lateral pectoral nerve block in combination with interscalene nerve block on opioid consumption and pain on awake shoulder arthroscopy patients - A feasibility study | |||||||||||||
| Medical condition: Peri- and postoperative pain after shoulder arthroscopy | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-005710-34 | Sponsor Protocol Number: Acide_Tranexamique | Start Date*: 2022-02-21 | |||||||||||
| Sponsor Name:Polyclinique Jean Villar - Bruges | |||||||||||||
| Full Title: Benefits on post-operative pain of intraoperative tranexamic acid administration during shoulder arthroscopy. | |||||||||||||
| Medical condition: Shoulder arthroscopy. | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-005838-15 | Sponsor Protocol Number: 01-10122020 | Start Date*: 2021-03-22 | |||||||||||
| Sponsor Name:Aarhus University Hospiotal | |||||||||||||
| Full Title: The effect of iliopsoas plane block on opioid consumption and pain after hip arthroscopy A double-blind randomized, controlled trial | |||||||||||||
| Medical condition: Postoperative pain after hip arthroscopy | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-006575-42 | Sponsor Protocol Number: 01_29112021 | Start Date*: 2022-03-08 | |||||||||||
| Sponsor Name:Aarhus University Hospital | |||||||||||||
| Full Title: The effect of subpectineal obturator nerve block on opioid consumption and pain after hip arthroscopy A double blind randomized controlled trial | |||||||||||||
| Medical condition: Postoperative pain after hip arthroscopy | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-001728-10 | Sponsor Protocol Number: 0890/WASH/2007 | Start Date*: 2007-09-12 | |||||||||||
| Sponsor Name:Sussex NHS Research Consortium | |||||||||||||
| Full Title: Post-operative analgesia for day-case ankle arthroscopy: Comparison of intra-articular racemic (RS)-bupivicaine with S(-)-bupivicaine. | |||||||||||||
| Medical condition: ankle arthroscopy | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001215-24 | Sponsor Protocol Number: 7-190320 | Start Date*: 2020-05-12 | |||||||||||
| Sponsor Name:Aarhus University Hospital | |||||||||||||
| Full Title: The effect of subpectineal obturator nerve block on opioid consumption and pain after hip arthroscopy A double-blind randomized, controlled trial | |||||||||||||
| Medical condition: Postoperative pain after hip arthroscopy | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-002559-27 | Sponsor Protocol Number: 2017-03 | Start Date*: 2018-03-29 | 
| Sponsor Name:Zaans Medisch Centrum | ||
| Full Title: ED50 and ED90 of intrathecal 1% chloroprocaine in day-case knee arthroscopy | ||
| Medical condition: Patients scheduled for ambulatory knee arthroscopy surgery receive intrathecal chloroprocaine | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-002208-32 | Sponsor Protocol Number: PAR06 | Start Date*: 2006-08-14 | 
| Sponsor Name:York Hospital NHS Trust | ||
| Full Title: A comparison of the analgesic efficacy of oral and intravenous paracetamol (perfalgan) in a day case setting | ||
| Medical condition: We will perform a double blind randomised comparison of oral paracetamol versus intravenous paracetamol (Perfalgan) in patients undergoing knee arthroscopy in a day surgery setting. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-001944-13 | Sponsor Protocol Number: ZAA15CPP | Start Date*: 2016-07-27 | 
| Sponsor Name:Zaans Medisch Centrum | ||
| Full Title: Chloroprocaine vs prilocaine for spinal anaesthesia in day-case surgery: a double-blind randomized trial | ||
| Medical condition: Patients scheduled for ambulatory knee arthroscopy surgery receive one of the two spinal anaesthetics | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-006125-28 | Sponsor Protocol Number: AT 15/10/07 | Start Date*: 2007-12-17 | 
| Sponsor Name:University Hospitals Leuven | ||
| Full Title: Comparison of intrathecal low-dose ropivacaine, bupivacaine and lidocaine for knee arthroscopy in ambulatory setting. a randomised, double-blind trial; | ||
| Medical condition: Male and female patients, scheduled for an elective knee arthroscopy. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-003675-11 | Sponsor Protocol Number: AT06/2011 | Start Date*: 2011-09-21 | 
| Sponsor Name:University Hospitals Leuven | ||
| Full Title: Comparison of 2-chloroprocaïne, bupivacaïne and lidocaïne for spinal anesthesia in knee artroscopy in an outpatient setting: a double blind randomised trial | ||
| Medical condition: spinal anesthesia in knee arthroscopy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-004817-16 | Sponsor Protocol Number: MACI00206 | Start Date*: 2008-01-23 | ||||||||||||||||
| Sponsor Name:Genzyme Europe B.V. | ||||||||||||||||||
| Full Title: A Prospective, Randomized, Open-Label, Parallel-Group, Multicenter Study to Demonstrate the Superiority of Matrix-induced Autologous Chondrocyte Implantation (MACI® implant) versus Arthroscopic Mi... | ||||||||||||||||||
| Medical condition: Symptomatic Articular Cartilage Defects of the Femoral Condyle including the Trochlea. osteochondritis dissecans lesions that do not require a bone graft. | ||||||||||||||||||
| 
 | ||||||||||||||||||
| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) CZ (Completed) SE (Completed) NL (Completed) PL (Completed) DE (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2006-003513-40 | Sponsor Protocol Number: Bupi-Cata-TYKS-version 1.0. | Start Date*: 2006-08-21 | |||||||||||
| Sponsor Name:Kalevi Pihlajamäki | |||||||||||||
| Full Title: Intrathecal bupivacaine and clonidine for ambulatory knee arthroscopy | |||||||||||||
| Medical condition: Patients are submitted for ambulatory knee arthroscopy | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-000098-35 | Sponsor Protocol Number: ANEPRO_2016_78 | Start Date*: 2017-07-31 | 
| Sponsor Name:SERVICIO DE ANESTESIOLOGÍA Y REANIMACIÓN HOSPITAL UNIVERSITARIO LA PAZ | ||
| Full Title: COMPARATIVE STUDY OF NAUTICS AND VOMITING IN THREE ANESTHETICAL REGIMENS: INTRAVENOUS, INHALATORY AND MIXED. | ||
| Medical condition: Arthroscopy for Temporomandibular | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-005613-14 | Sponsor Protocol Number: REUM-2021-01 | Start Date*: 2023-03-13 | 
| Sponsor Name: | ||
| Full Title: Immune-Related Rheumatological Adverse Events study. Data collection from patients with cancer to evaluate rheumatological adverse events in patients treated with immune-checkpoint inhibitors. | ||
| Medical condition: Any cancer patients starting immune checkpoint inhibitor therapy (ICI-therapy). Any patient exhibiting a rheumatological immune-related adverse event (R-irAE). Patients with newly developed rheum... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-000062-35 | Sponsor Protocol Number: ThereIsNoSponsorInvolved | Start Date*: 2011-04-05 | |||||||||||
| Sponsor Name:Mikko Pitkänen, MD, PhD | |||||||||||||
| Full Title: Artikaiini 40mg ja kloroprokaiini 40 mg päiväkirurgisina spinaalipuudutteina (Lyhenne: A40C40) | |||||||||||||
| Medical condition: Knee arthroscopy performed as day case surgery | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-002123-41 | Sponsor Protocol Number: anakinrapain1 | Start Date*: 2013-10-21 | |||||||||||
| Sponsor Name:Lovisenberg Diaconal Hospital | |||||||||||||
| Full Title: Effects of intraarticular IL1-Ra on pain and inflammatory mediators after knee arthroscopy –a double blind, placebo controlled study using microdialysis technique | |||||||||||||
| Medical condition: Post operative pain after diagnostic or therapeutic knee arthroscopy | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-000379-18 | Sponsor Protocol Number: 1.0 | Start Date*: 2012-05-04 | 
| Sponsor Name:Medizinische Universität Wien, Universitätsklinik für Klinische Pharmakologie | ||
| Full Title: Plasma and synovial fluid pharmacokinetics of cefuroxime and linezolid in patients undergoing elective knee arthroscopy after a single intravenous dose of cefuroxime and linezolid: an exploratory m... | ||
| Medical condition: Subjects under general anaesthesia after a knee surgery get a microdialysis probe insertio into the operated knee and a probe insertion into the thigh on the contralateral side. After the operation... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-014717-27 | Sponsor Protocol Number: 2009/4:7 | Start Date*: 2009-12-22 | 
| Sponsor Name:Karolinska Institutet/Södersjukhuset | ||
| Full Title: Betametasone as postoperative pain treatment for knee arthroscopies at a day surgical center | ||
| Medical condition: Unspecified knee pain investigated by an arthroscopy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-004087-30 | Sponsor Protocol Number: 1007612/30.04.2010 | Start Date*: 2011-08-25 | |||||||||||
| Sponsor Name:Tartu University Department of Sports Medicine and Rehabilitation | |||||||||||||
| Full Title: Effect of 12 weeks rehabilitation (aspect of neuromuscular physical therapy) in middle-aged patients in post-atroscopic period | |||||||||||||
| Medical condition: Cartilage Lesion of the Knee Joint | |||||||||||||
| 
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: EE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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