- Trials with a EudraCT protocol (41)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (16)
41 result(s) found for: Ketorolac.
Displaying page 2 of 3.
EudraCT Number: 2014-002215-42 | Sponsor Protocol Number: 22/13 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:IRCCS Burlo Garofolo | |||||||||||||
Full Title: Single-blind randomized controlled trial for acute abdomen analgesia in Pediatric Emergency department | |||||||||||||
Medical condition: Analgesia in pediatric acute abdominal pain | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001373-26 | Sponsor Protocol Number: IC01/03/DKP(12-Kef) | Start Date*: 2004-11-15 | |||||||||||
Sponsor Name:Laboratorios Menarini, S.A | |||||||||||||
Full Title: Multicentre clinical trial to evaluate the efficacy and safety of dexketoprofen trometamol (50 mg t.i.d.) versus ketorolac (30 mg t.i.d.) and placebo by intravenous route, as part of balanced analg... | |||||||||||||
Medical condition: elective orthopedic surgery (hip arthroplasty) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004890-21 | Sponsor Protocol Number: NL72427.068.19 | Start Date*: 2021-01-18 |
Sponsor Name:Academic Hospital Maastricht (azM) | ||
Full Title: Effectiveness of Periocular drug Injection in CATaract surgery | ||
Medical condition: cystoid macular edema (CME) | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) DE (Prematurely Ended) AT (Prematurely Ended) PT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2013-002439-10 | Sponsor Protocol Number: PAKA-33601-AS117013 | Start Date*: 2013-10-23 | |||||||||||
Sponsor Name:University of Warwick
[...]
1. University of Warwick
2. University Hospitals Coventry & Warwickshire NHS Trust |
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Full Title: Perioperative Analgesia for Knee Arthroplasty: A prospective randomised controlled trial | |||||||||||||
Medical condition: Osteoarthritis of the knee is a common problem; it causes inability to walk without pain and a reduction in activity levels. Total knee replacements are performed for relief of this disabilitating ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005110-30 | Sponsor Protocol Number: FASTRELIEF | Start Date*: 2017-02-23 | ||||||||||||||||
Sponsor Name:FONDAZIONE IRCCS "ISTITUTO NAZIONALE DEI TUMORI" | ||||||||||||||||||
Full Title: A multicenter randomized trial to evaluate the efficacy of fentanyl pectin nasal spray (FPNS) versus Physician Choice (PC) - Usual Care (UC), in reducing incidental predictable breakthrough pain (I... | ||||||||||||||||||
Medical condition: Patients with head and neck cancer . | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-008723-15 | Sponsor Protocol Number: 2009-01 | Start Date*: 2009-04-22 |
Sponsor Name:Örebro University Hospital | ||
Full Title: Postoperative Pain Relief following Total Hip Arthroplasty. A comparison between Intrathecal morphine (IM) and Local Infiltration Analgesia (LIA). | ||
Medical condition: Postoperative pain following total hip arthroplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-013645-29 | Sponsor Protocol Number: 120609 | Start Date*: 2009-08-07 |
Sponsor Name:Epsom & St Helier's University Hospital NHS Trust | ||
Full Title: A Two Phase Prospective Randomized Control Trial of Infiltrated Periarticular Multimodal Analgesia following Primary Total Hip Replacement | ||
Medical condition: Pain relief after total hip replacement | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003885-15 | Sponsor Protocol Number: OMS302-ILR-006 | Start Date*: 2014-01-06 | |||||||||||
Sponsor Name:Omeros Corporation | |||||||||||||
Full Title: A Phase 3 Randomised, Double-Masked, Placebo-Controlled Study of the Effect of OMS302 on Intraoperative Pupil Diameter in Subjects at High Risk of Intraoperative Floppy Iris Syndrome Undergoing Int... | |||||||||||||
Medical condition: Intraocular Lens Replacement (ILR) in subject at high risk for Intraoperative Floppy Iris Syndrome (IFIS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Prematurely Ended) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000867-25 | Sponsor Protocol Number: OMS302-ILR-004 | Start Date*: 2012-07-23 | |||||||||||
Sponsor Name:Omeros Corporation | |||||||||||||
Full Title: A Phase 3 Randomised, Double-Masked, Placebo-Controlled Study of the Pharmacokinetics of OMS302 and the Effect of OMS302 on Intraoperative Pupil Diameter and Early Postoperative Pain in Subjects Un... | |||||||||||||
Medical condition: Intraocular Lens Replacement with Pharmacoemulsification | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005263-31 | Sponsor Protocol Number: LEVOKETO_02-2020 | Start Date*: 2021-06-02 | |||||||||||
Sponsor Name:NTC SRL | |||||||||||||
Full Title: Assessment of the effects and tolerability of RD03/2016 (Levofloxacin; Ketorolac Trometamol 0.5+0.5% w/v eye drops solution) for the treatment of bacterial conjunctivitis in adults: a multicentre, ... | |||||||||||||
Medical condition: Bacterial conjunctivitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) IT (Completed) DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000432-27 | Sponsor Protocol Number: 5/2006/O/Sper | Start Date*: 2006-03-16 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Epidural analgesia vs systemic intravenous analgesia in the major gynecological surgery | |||||||||||||
Medical condition: increased isteroannessiectomia, isteroannessiectomia with linfoadenectomia, annessiectomia with linfoadenectomia with omentectomia, removal focus of endometriosis 4 stage | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000938-35 | Sponsor Protocol Number: 1SPR11001 | Start Date*: 2013-06-22 | |||||||||||
Sponsor Name:Luitpold Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Single Arm, Open Label Study to compare the Pharmacokinetics, Safety, and Efficacy of SPRIX® (intranasal ketorolac tromethamine) in 12 to 17 Year-Old Patients vs. Adult Patients (18 - 64 Years) U... | |||||||||||||
Medical condition: post open surgery pain (incuding but not limited to orthopedic, abdominal, thoracic, plastic/reconstructive, neurologic [spine], or urologic procedures) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003875-20 | Sponsor Protocol Number: 2012-09 | Start Date*: 2013-01-02 | |||||||||||
Sponsor Name:Universitetssjukhuset Örebro | |||||||||||||
Full Title: Postoperative pain relief following total hip arthroplasty. A comparison between 3-in-1 blockade (single shot) with ultrasound placement and local infiltration analgesia. | |||||||||||||
Medical condition: Postoperative pain relief after total hip arthroplasty | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018600-87 | Sponsor Protocol Number: Peri-Trauma | Start Date*: 2010-02-24 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA` DI NOVARA | |||||||||||||
Full Title: POST-OPERATIVE PAIN CONTROL OF PEDIATRIC PATIENTS UNDERWENT ORTHOPEDIC SURGERY: COMPARISON OF INTRAVENOUS ANALGESIA AND ONE-SHOT EPIDURAL LUMBAR NERVE BLOCK. | |||||||||||||
Medical condition: POST-OPERATIVE PAIN CONTROL OF PEDIATRIC PATIENTS UNDERWENT ORTHOPEDIC SURGERY | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000736-26 | Sponsor Protocol Number: 206207-014 | Start Date*: 2006-05-17 |
Sponsor Name:Allergan Limited | ||
Full Title: An 8-Week, Multicenter, Masked, Randomized Trial (with an 18-Week Masked Extension) to Assess the Safety and Efficacy of 700 µg and 350 µg Dexamethasone Posterior Segment Drug Delivery System (DEX ... | ||
Medical condition: Non-infectious ocular inflammation of the posterior segment in intermediate or posterior uveitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) AT (Completed) IT (Completed) PT (Completed) BE (Completed) CZ (Completed) DE (Completed) GR (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-002170-39 | Sponsor Protocol Number: Knemo01 | Start Date*: 2017-09-14 | |||||||||||
Sponsor Name:Eksote | |||||||||||||
Full Title: Combination of intrathecal morphine and local infiltration analgesia in treatment postoperative pain of total knee arthroplasty | |||||||||||||
Medical condition: Postoperative pain after total knee arthroplasty | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003343-35 | Sponsor Protocol Number: CR-TFB-2014/502 | Start Date*: 2014-10-01 | |||||||||||
Sponsor Name:Thomas Fichtner Bendtsen | |||||||||||||
Full Title: The effect of saphenous nerve and obturator nerve block combined with systemic high dose glucocorticoid versus local infiltration analgesia combined with a systemic high dose glucocorticoid on opi... | |||||||||||||
Medical condition: The medical condition to be examined in this study is the first postoperative period after total knee replacement with a view to pain management. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002666-47 | Sponsor Protocol Number: SOAP1 | Start Date*: 2017-11-02 | |||||||||||
Sponsor Name:Dpt. of Ophthalmology, Rigshospitalet-Glostrup | |||||||||||||
Full Title: Effect of drop-less surgery compared to topical NSAID alone and combination of steroid and NSAID on central macular thickness after cataract surgery, a randomized controlled trial | |||||||||||||
Medical condition: Postoperative cystoid macular edema following cataract surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024315-14 | Sponsor Protocol Number: 95609379 | Start Date*: 2011-01-04 | |||||||||||
Sponsor Name:Tekonivelsairaala Coxa | |||||||||||||
Full Title: Paikallispuudutus polven tekonivelleikkauksen yhteydessä - vähentynyt opiaattien kulutus leikkauksen jälkeen ja nopeampi liikeharjoituksen aloitus - kaksoissokkotutkimus | |||||||||||||
Medical condition: Polven nivelrikko. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016445-25 | Sponsor Protocol Number: 2010-KVA | Start Date*: 2010-01-07 | ||||||||||||||||
Sponsor Name:Ortopædkirurgisk Afd. E, Århus Universitetshospital | ||||||||||||||||||
Full Title: Undersøgelse af postoperative bolus infusioner ved primær hoftealloplastik | ||||||||||||||||||
Medical condition: Patienter med hofteartrose der indlægges til primær total hoftealloplastik | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
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