- Trials with a EudraCT protocol (5,833)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (321)
5,833 result(s) found for: Surgery.
Displaying page 9 of 292.
EudraCT Number: 2018-001430-18 | Sponsor Protocol Number: 5101127 | Start Date*: 2019-08-12 |
Sponsor Name:Kuopio University Hospital | ||
Full Title: Does postoperative intravenous corticosteroid and intravenous beta blocker management prevent atrial fibrillation after cardiac surgery? | ||
Medical condition: new onset atrial fibrillation and paroxysmal atrial fibrillation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001761-42 | Sponsor Protocol Number: 0869-131 | Start Date*: 2006-06-12 | |||||||||||
Sponsor Name:Merck & Co., Inc | |||||||||||||
Full Title: A Randomized, Double-Blind, Active Comparator-Controlled, Parallel-Group Study Conducted Under In-House Blinding Conditions, to Examine the Safety, Tolerability, and Efficacy of Aprepitant for the ... | |||||||||||||
Medical condition: Postoperative Nausea and Vomiting | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-005287-24 | Sponsor Protocol Number: BAR104 | Start Date*: 2005-06-28 |
Sponsor Name:Univ.-Kl. f.Augenheilkunde und Optometrie Wien | ||
Full Title: Effect of diclofenac-sodium, unpreserved diclofenac-sodium or ketorolac on the inflammatory response after cataract surgery | ||
Medical condition: intraocular inflammatory reaction after cataract-surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-002309-39 | Sponsor Protocol Number: 60/2011 | Start Date*: 2016-07-08 |
Sponsor Name:Osakidetza | ||
Full Title: EFFECTIVENESS OF ROPIVACAINE 0.1% INTRAPERITONEAL IN POSTOPERATIVE PAIN CONTROL IN GYNECOLOGIC LAPAROSCOPIC SURGERY " | ||
Medical condition: EFECTIVENESS OF ROPIVACAINE 0,1% FOR PAIN CONTROL AFTER LAPAROSCOPIC GYNECOLOGICAL SURGERY | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001852-11 | Sponsor Protocol Number: ARG1 | Start Date*: 2006-10-13 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Influence of L-Arginine on perfusion in patients receiving peripheral bypass surgery (Einfluss von L-Arginin auf die Perfusion bei Patienten mit peripheren Bypassoperationen) | ||
Medical condition: In general, ischemia and reperfusion are main causes for tissue damage and consequently for organ damage after surgery. Particularily, patients suffering from a peripheral occlusive disease show a ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-000135-47 | Sponsor Protocol Number: 21/103 | Start Date*: 2021-11-02 |
Sponsor Name:Hospital Universitario Fundación Alcorcón | ||
Full Title: Analgesic efficacy of erector spinae plane block in lumbar spine surgery: a prospective, randomized and double blind study. | ||
Medical condition: The analgesic efficacy of erector spinae plane block in lumbar spine surgery. Infiltration of local anesthetic in this plane may lower postoperative pain. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001079-35 | Sponsor Protocol Number: PRPK | Start Date*: 2019-08-29 |
Sponsor Name:Cliniques universitaires Saint-Luc | ||
Full Title: A prospective randomized study in ambulatory patients undergoing upper limb bone surgery under single shot axillary plexus block. | ||
Medical condition: Do patients who are very painful when the axillary block wears off after bone surgery of the upper limb have a pre-existing central sensitization? Could this “rebound pain” be prevented by pre-inc... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-002494-19 | Sponsor Protocol Number: NL61864.041.17 | Start Date*: 2017-12-21 |
Sponsor Name:UMC Utrecht | ||
Full Title: Dexamethasone for Cardiac Surgery trial: a novel 'Standard Practice Preference-Randomised Consent' Design. A PILOT STUDY | ||
Medical condition: Inflammatory response to cardiac surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2020-000638-17 | Sponsor Protocol Number: 44107 | Start Date*: 2021-03-30 |
Sponsor Name:Oslo University Hospital | ||
Full Title: ZOLEDRONATE EARLY TO HIP FRACTURE PATIENTS – SAFE AND EFFECTIVE? A DOUBLE-BLINDED RANDOMIZED CONTROLLED TREATMENT STRATEGY TRIAL ON ZOLEDRONATE IN HIP FRACTURE PATIENTS THE ZEBRA TRIAL | ||
Medical condition: Osteoporosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001714-29 | Sponsor Protocol Number: 290975 | Start Date*: 2017-08-09 |
Sponsor Name:Helsinki University hospital | ||
Full Title: Influence of epidural analgesia on opioid consumption and patients recovery after laparoskopic colorectal surgery. | ||
Medical condition: Compare epidural and conventional pain treatment after laparoskopic colorectal surgery. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004514-10 | Sponsor Protocol Number: 00173 | Start Date*: 2017-03-08 |
Sponsor Name:Raimo Tuuminen | ||
Full Title: Pre and post-operative corticosteroid and NSAID combination treatment in cataract surgery of diabetic patient | ||
Medical condition: Cataract senilis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004784-40 | Sponsor Protocol Number: 00176 | Start Date*: 2017-03-03 |
Sponsor Name:Raimo Tuuminen | ||
Full Title: Anti-inflammatory medication in cataract surgery of pseudoexfoliation eyes | ||
Medical condition: Cataract senilis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-000992-12 | Sponsor Protocol Number: HIPP-CABG | Start Date*: 2008-03-27 |
Sponsor Name:Academic Medical Center | ||
Full Title: Organ protection by noble gases – A clinical study to investigate Helium induced Pre- and Postconditioning in patients undergoing coronary artery bypass surgery (HIPP-CABG). | ||
Medical condition: patients undergoing coronary artery bypass surgery, helium induced pre- and postconditioning | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004083-62 | Sponsor Protocol Number: steroid3848 | Start Date*: 2019-09-06 |
Sponsor Name:Semmelweis University, Oro-Maxillofacial Surgery and Stomatology | ||
Full Title: Effect of preoperative intramasseteric methylprednisolone injection on the post-operative sequelae of lower third molar surgery: a placebo controlled, randomized, double-blinded study | ||
Medical condition: post-operative swelling, trismus, pain | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004713-91 | Sponsor Protocol Number: ROPISPINE | Start Date*: 2015-02-09 |
Sponsor Name:Universitair Ziekenhuis Brussel | ||
Full Title: Epidural ropivacaine as part of a multimodal postoperative pain treatment following thoracolumbar spinal fusion surgery. | ||
Medical condition: Spine Surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-004038-28 | Sponsor Protocol Number: Zalviso | Start Date*: 2018-02-21 |
Sponsor Name:Universitair Ziekenhuis Brussel | ||
Full Title: Comparative Prospective Randomized Study in Postoperative Cardiac Surgery Patients on Analgesia with Morphine Continuous Infusion or Sublingual Sufentanil (Zalviso®). | ||
Medical condition: -Postoperative pain treatment after cardiac surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-004465-32 | Sponsor Protocol Number: 2011/386 | Start Date*: 2011-12-12 | |||||||||||
Sponsor Name:Dept. of Cardiothoracic & Vascular Surgery, Aarhus University Hospital, Skejby | |||||||||||||
Full Title: Can post-operative treatment with parathyroid hormone enhance bone healing and quality of newly formed bone after sternotomy in cardiac surgery patients? | |||||||||||||
Medical condition: Sternotomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004990-24 | Sponsor Protocol Number: ZKS000529 | Start Date*: 2008-05-05 | |||||||||||
Sponsor Name:University Medical Center Freiburg | |||||||||||||
Full Title: Comparison of the concentrations of the antibiotic compound Daptomycin in serum, cartilage-, muscle and subcutaneous tissue after a preoperative intravenous administration (Klinische Studie zum ... | |||||||||||||
Medical condition: Elective orthopedic surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002096-29 | Sponsor Protocol Number: iVRCT | Start Date*: 2015-07-20 | ||||||||||||||||
Sponsor Name:Speising Orthopaedic Hospital Vienna | ||||||||||||||||||
Full Title: Application of Intrawound Vancomycin Powder in Spinal Fusion Surgery to Reduce Postoperative Surgical Site Infections - A Prospective Randomized Controlled Trial | ||||||||||||||||||
Medical condition: Postoperative surgical site infections (deep and superficial) after spinal fusion surgery | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005124-14 | Sponsor Protocol Number: 2005DICPAED | Start Date*: 2007-07-12 | |||||||||||
Sponsor Name:Joint Sponsor: University of Glasgow with NHS greater Glasgow and Clyde [...] | |||||||||||||
Full Title: The unlicensed and off-label use of diclofenac in paediatric patients: Pharmacokinetic, pharmacodynamic and pharmacogenomic evlauations | |||||||||||||
Medical condition: Children undergoing surgery for orthapaedic, ENT, renal or abdominal conditions | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
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