- Trials with a EudraCT protocol (68)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
68 result(s) found for: Hand surgery.
Displaying page 1 of 4.
EudraCT Number: 2017-002130-23 | Sponsor Protocol Number: TQLnephrectomi_v_1 | Start Date*: 2017-07-28 |
Sponsor Name:Zealand university hospital Roskilde | ||
Full Title: Ultrasoundguided Transmuscular Quadratus Lumborum(TQL) block for hand assisted laparoscopic nephrectomy - a randomized controlled trial | ||
Medical condition: The postoperative pain after Hand assisted lap.nephrectomy operation.Our one year retrospective study of patients with Kidney cancer treated with Hand assisted lap.nephrectomy revealed that, 71% of... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-001221-13 | Sponsor Protocol Number: 2639063 | Start Date*: 2013-10-10 | |||||||||||
Sponsor Name:Akershus university hospital | |||||||||||||
Full Title: Dupytren’s disease study A randomized controlled trial comparing clostridium histolyticum with needle aponeurotomy. | |||||||||||||
Medical condition: Dupytren’s disease, primary MCP joint contractures of the third, forth and fifth finger of the hand. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002630-22 | Sponsor Protocol Number: RC31/17/0041 | Start Date*: 2018-01-18 | |||||||||||
Sponsor Name:University Hospital of Toulouse | |||||||||||||
Full Title: Pain prevention during propofol infusion in pediatric: hypnoanalgesia of the hand versus lidocaine. | |||||||||||||
Medical condition: surgery under general anaesthetic | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004251-76 | Sponsor Protocol Number: 87230 | Start Date*: 2017-05-22 | ||||||||||||||||
Sponsor Name:University Hospitals of Leicester NHS Trust | ||||||||||||||||||
Full Title: A pragmatic multi-centre randomised controlled non-inferiority, cost effectiveness trial comparing injections of collagenase into the cord to surgical correction in the treatment of moderate Dupuyt... | ||||||||||||||||||
Medical condition: Dupuytren's contracture | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001780-40 | Sponsor Protocol Number: 11069 | Start Date*: 2015-05-21 | |||||||||||
Sponsor Name:University of Oxford, Clinical Trials and Research Governance | |||||||||||||
Full Title: A multi-centre, double blind, randomised, placebo-controlled, parallel group, phase II trial to determine the efficacy of intra-nodular injection of anti-TNF to control disease progression in early... | |||||||||||||
Medical condition: Dupuytren's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
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: 2016-002325-11 | Sponsor Protocol Number: AT052016 | Start Date*: 2016-07-27 |
Sponsor Name:Univerity Hospital Leuven | ||
Full Title: Intravenous regional anesthesia versus axillar block for hand surgery in day-care hospitall: A prospective, randomised, comparative trial | ||
Medical condition: intra and post operative pain management | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-000537-69 | Sponsor Protocol Number: PROP2% | Start Date*: 2015-09-21 |
Sponsor Name:Universitair Ziekenhuis Brussel | ||
Full Title: Real time monitoring of blood propofol concentration | ||
Medical condition: - General anaesthesia - Pharmacokinetics and Pharmacodynamics of Propofol - Inflammatory parameters - Elective thyroid, oncologic breast,ENT or cervical arthrodesis surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001704-38 | Sponsor Protocol Number: NL40000.072.012 | Start Date*: 2012-06-14 | |||||||||||
Sponsor Name:Sint Maartenskliniek | |||||||||||||
Full Title: Effect of local anesthetic dose versus volume on block duration of single shot ultrasound-guided axillary brachial plexus block with mepivacaine | |||||||||||||
Medical condition: Patients scheduled for single shot axillary brachial plexus block for hand, wrist, or forearm orthopedic surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006652-22 | Sponsor Protocol Number: AN08/8751 | Start Date*: 2009-06-03 |
Sponsor Name:Leeds Teaching Hospital NHS Trust | ||
Full Title: A multicentre, randomised, double blind, evaluative comparison trial of Rapydan® patch and Ametop® gel for topical anaesthesia during venous cannulation in adults admitted to hospital for day-case ... | ||
Medical condition: ASA 1 and 2 patients admitted for Day case surgery- assessment of cannulation pain after topical anaesthetic applications. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-003087-40 | Sponsor Protocol Number: PHRC-N-2015 | Start Date*: 2017-01-17 |
Sponsor Name:UHangers | ||
Full Title: Interest of intraveinous iron and tranexamic acid to reduce transfusion in hip fracture patients - HIFIT Study | ||
Medical condition: Hip fracture | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-005758-39 | Sponsor Protocol Number: 9812/A | Start Date*: 2006-08-16 |
Sponsor Name:Greater Glasgow Health Board | ||
Full Title: Effect site controlled, reaction time safeguarded, patient maintained sedation with Propofol A) in oral surgery patients B) in general dentistry patients C) in colonoscopy patients | ||
Medical condition: No specific medical condition. IMP will be used to provide conscious sedation for patients undergoing potentially unpleasant procedures including dentistry and colonoscopy. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-000717-31 | Sponsor Protocol Number: WI187847 | Start Date*: 2015-06-09 | |||||||||||
Sponsor Name:UZ Leuven | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled study of celecoxib after collagenase injection for adults with Dupuytren’s disease at high risk of recurrence | |||||||||||||
Medical condition: Dupuytren's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003694-34 | Sponsor Protocol Number: 2-HIT | Start Date*: 2017-10-25 | ||||||||||||||||
Sponsor Name:Ziekenhuis Oost-Limburg | ||||||||||||||||||
Full Title: Onset and duration of Forearm nerve blockade performed with a single distal injection versus sequential injections at distal and proximal locations alongside the nerves: a blinded randomized contro... | ||||||||||||||||||
Medical condition: Dupuytren contrature and Carpal Tunnel syndrome | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000516-28 | Sponsor Protocol Number: 39032 | Start Date*: 2012-06-14 |
Sponsor Name:University Medical Centre Groningen | ||
Full Title: A prospective clinical study on the efficacy of collagenase clostridium histolyticum (CCH) injections in the thumb and first web space contractures in Dupuytren's Disease | ||
Medical condition: Dupuytren's Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-011829-13 | Sponsor Protocol Number: AN09/8905 | Start Date*: 2009-11-02 |
Sponsor Name:University of Leeds | ||
Full Title: What is the ED95 dose for bupivacaine for supraclavicular brachial plexus block using ultrasound? | ||
Medical condition: Patients presenting for routine upper limb surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-022971-79 | Sponsor Protocol Number: PALO-10-14 | Start Date*: 2011-05-23 | ||||||||||||||||
Sponsor Name:Helsinn Healthcare SA | ||||||||||||||||||
Full Title: A Multicenter, Double-blind, Double-dummy, Randomized, Parallel Group, Stratified Study to Evaluate the Efficacy and Safety of a Single IV Dose of Palonosetron Compared to a Single IV Dose of Ondan... | ||||||||||||||||||
Medical condition: Postoperative nausea and vomiting (PONV) | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Completed) PL (Completed) HU (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-000604-25 | Sponsor Protocol Number: R96-A6604-14-S22 | Start Date*: 2015-05-02 |
Sponsor Name:Danish Cancer Society Research Center | ||
Full Title: HBOT LYCA: Hyperbaric Oxygen Therapy to reduce Lymphoedema after Breast Cancer - an explorative clinical trial | ||
Medical condition: breast cancer related lymphedema | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-005006-31 | Sponsor Protocol Number: EML053774_002 | Start Date*: 2007-04-03 |
Sponsor Name:Merck Sante France | ||
Full Title: A randomized, stratified on age, parallel group design study to investigate the safety, tolerability and pharmacokinetics after a 60 minutes application of 4% lidocaine cream compared to EMLA® crea... | ||
Medical condition: Topical anesthesia of healthy skin before venous or subcutaneous puncture, before superficial cutaneous instrumental surgery or laser beam (tattoo or cutaneousangioma) | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-006143-31 | Sponsor Protocol Number: AUX-CC-854.01 | Start Date*: 2007-10-19 | |||||||||||
Sponsor Name:Auxilium UK Limited | |||||||||||||
Full Title: A Phase 3, Open Label Study of Safety and Efficacy of AA4500 in the Treatment of Subjects With Dupuytren's Contracture | |||||||||||||
Medical condition: Dupuytren's Contracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) DK (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
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