- Trials with a EudraCT protocol (188)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
188 result(s) found for: Shoulder.
Displaying page 1 of 10.
EudraCT Number: 2007-001709-85 | Sponsor Protocol Number: 10.05.7 | Start Date*: 2007-11-13 | |||||||||||
Sponsor Name:South Eastern Health and Social Care Trust | |||||||||||||
Full Title: Treatment of Shoulder Capsulitis by single or Multiple Corticosteroid Injections | |||||||||||||
Medical condition: Capsulitis of the Shoulder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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 (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000147-27 | Sponsor Protocol Number: TH/RCT2/0001 | Start Date*: 2012-07-30 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: A Single-Blind Randomised Controlled Pilot trial of Corticosteroid Injection for Shoulder Pain | |||||||||||||
Medical condition: Rotator cuff tendinopathy Adhesive capsulitis of the shoulder joint | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000335-25 | Sponsor Protocol Number: TYKS Bupi-Fenta version 1 | Start Date*: 2007-05-16 | |||||||||||
Sponsor Name:Riika Merivirta | |||||||||||||
Full Title: Treatment of postoperative pain after arthroscopic shoulder surgery, a comparison between a fentanyl patch and local anaesthetic | |||||||||||||
Medical condition: Healthy patients who need arthroscopic shoulder surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004612-19 | Sponsor Protocol Number: IIBSP-COR-2017-98 | Start Date*: 2018-03-20 |
Sponsor Name:Institut de Recerca Hospital de la Santa Creu i Sant Pau | ||
Full Title: EFFICACY OF THE SUPRAESCAPULAR NERVE APPROACH WITH CORTICOIDS ADMINISTRATION VERSUS PULSED RADIOFREQUENCY IN CHRONIC SHOULDER PAIN. DOUBLE BLIND RANDOMIZED CLINICAL TRIAL | ||
Medical condition: Chronic shoulder pain | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000235-27 | Sponsor Protocol Number: S-20120216 | Start Date*: 2013-02-19 | |||||||||||
Sponsor Name:Odense universitets Hospital | |||||||||||||
Full Title: Interscalener blockade for surgery on the shoulder, a comparison of two dosing regimens: Fixed intermittent bolus with the possibility of PCA (Patient controlled administration) Vs. continuous infu... | |||||||||||||
Medical condition: Shoulder frcture Rotator cuff leasion Shoulder alluplastic | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021224-10 | Sponsor Protocol Number: interscalaenus block 1.0 | Start Date*: 2010-09-02 |
Sponsor Name:Universitätsklinik für Anästhesie,Intesivmedizin und Schmerztherapie,Mediniz.Universität Wien | ||
Full Title: The Impact of Interscalene Brachial Plexus Blockade on Postoperative Function after Shoulder Surgery | ||
Medical condition: The impact of interscalene brachial plexus blockade on postoperative function after shoulder surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-002991-28 | Sponsor Protocol Number: N/A | Start Date*: 2016-10-24 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: GRASP: Getting it Right: Addressing Shoulder Pain. Clinical and cost effectiveness of progressive exercise compared to best practice advice, with or without corticosteroid injection, for the treat... | |||||||||||||
Medical condition: Rotator Cuff Partial Tear (not full tear) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003082-15 | Sponsor Protocol Number: KTB-002 | Start Date*: 2011-09-08 | ||||||||||||||||
Sponsor Name:Karen Toftdahl Bjørnholdt | ||||||||||||||||||
Full Title: High dose dexamethasone for pain following arthroscopic shoulder surgery: A randomised blinded clinical trial. | ||||||||||||||||||
Medical condition: Pain following arthroscopic shoulder surgery. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003709-25 | Sponsor Protocol Number: PRPVol | Start Date*: 2019-06-11 |
Sponsor Name:Hospital Son Llatzer | ||
Full Title: Value of ultrasound-guided treatment with Platelet Rich Plasma or high volume injection in the rotator cuff tendon: Prospective randomized clinical trial. EudraCT number 2018-003709-25 | ||
Medical condition: Shoulder pain due to rotator cuff tendinopathy or partial tears of the supraspinatus tendon | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-000622-67 | Sponsor Protocol Number: 3147K2-101WW | Start Date*: 2005-06-03 |
Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc. | ||
Full Title: A Double-Blind, Placebo-Controlled, Randomized, Multiple Ascending Dose, Safety Study of MYO-029 Administered to Adult Patients with Becker, Facioscapulohumeral and Limb-Girdle Muscular Dystrophy. | ||
Medical condition: Becker Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Limb-Girdle Muscular Dystrophy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-003628-20 | Sponsor Protocol Number: 0705/789 | Start Date*: 2005-11-10 |
Sponsor Name:West Yorkshire Primary Care R&D Unit | ||
Full Title: The Shoulder Window of Opportunity Study (SWOP) - A pragmatic randomised trial comparing corticosteroid injection with timely physiotherapy with physiotherapy alone for older subjects with subacrom... | ||
Medical condition: Subacromial impingement syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002402-36 | Sponsor Protocol Number: 651 | Start Date*: 2015-08-27 |
Sponsor Name:Sint Maartenskliniek | ||
Full Title: Pharmacokinetic Profile of Liposome Bupivacaine (Exparel®) after Perineural Admission in the Interscalene Groove for Primary Total Shoulder Arthroplasty. | ||
Medical condition: patients receiving a primary total shoulder arthroplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004219-36 | Sponsor Protocol Number: MR-ISB-1 | Start Date*: 2013-12-02 |
Sponsor Name:Paracelsus Mediznische Privatuniversität, Universitätsklinik für Anästhesiologie, perioperative Medizin und Intensiv | ||
Full Title: Magnetic Resonance Imaging of Local Anesthetic Distribution: A Comparison of 5 and 15 milliliters of ropivacaine 0.75% for ultrasound guided interscalene plexus blockade | ||
Medical condition: Surgery of the shoulder and/or upper extremity using interscalene brachial plexus block | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001419-21 | Sponsor Protocol Number: RC19_0042 | Start Date*: 2019-09-16 |
Sponsor Name:CHU de Nantes | ||
Full Title: Optimization of skin preparation to reduce Cutibacterium acnes colonization in superficial and deep samples during prosthetic shoulder surgery in male patients | ||
Medical condition: Cutibacterium acnes infection in shoulder arthroplasty with males | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003855-12 | Sponsor Protocol Number: REDOLEV-2019 | Start Date*: 2020-01-07 |
Sponsor Name:Fundación Instituto de Investigación Sanitaria Aragón | ||
Full Title: Phase III Clinical Trial, single-center, randomized, double-blind, to demonstrate a lower incidence of acute diaphragmatic paralysis of the brachial plexus block with interscalene approach in arthr... | ||
Medical condition: Patients who will undergo surgery for arthroscopic shoulder surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002343-34 | Sponsor Protocol Number: KALK1183 | Start Date*: 2015-10-15 |
Sponsor Name:Martina Hansens Hospital | ||
Full Title: Treatment of calcific tendinitis of the Rotator Cuff A randomized, double blinded, sham controlled, international, multicenter study | ||
Medical condition: Calcific tendinitis of the shoulder | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003238-29 | Sponsor Protocol Number: BRN-C-2015-03 | Start Date*: 2016-04-06 |
Sponsor Name:Fundación Sociedad Española de Médicos de Atención Primaria (SEMERGEN) | ||
Full Title: Pilot phase II clinical trial, randomized, double-blind, controlled, single-center study to evaluate the efficacy and safety of Solanum malacoxylon 9CH in patients with calcific tendinitis of shoulder | ||
Medical condition: Calcific tendinitis of shoulder | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
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 (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002176-25 | Sponsor Protocol Number: 1510150 | Start Date*: 2016-04-01 |
Sponsor Name:Royal Devon and Exeter NHS Foundation Trust | ||
Full Title: Do ultrasound guided botulinum A injections relieve pain in rotator cuff arthropathy? | ||
Medical condition: Rotator Cuff Tear Arthropathy | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
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