- 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 7 of 292.
EudraCT Number: 2018-001305-82 | Sponsor Protocol Number: IC3627/18 | Start Date*: 2019-05-16 |
Sponsor Name:Laura Perelló Moreno | ||
Full Title: Study on the advantages of local post-operative infiltration in forefoot surgery. | ||
Medical condition: management of postoperative pain in ambulatory foot surgery that allows the realization of immediate rehabilitation and better functional results and personal satisfaction | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-006163-22 | Sponsor Protocol Number: PK-VIT-D | Start Date*: 2012-04-20 | |||||||||||
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | |||||||||||||
Full Title: Study to evaluate the pharmacokinetic of vitamin D (cholecalciferol) in patients with obesity after bariatric surgery in vitamin D deficiency and after normalization | |||||||||||||
Medical condition: Obese patients after bariatric surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002672-25 | Sponsor Protocol Number: STR001-201 | Start Date*: 2015-11-18 |
Sponsor Name:Strekin AG | ||
Full Title: A Phase II multicenter, placebo-controlled, proof-of-concept study evaluating the safety, and efficacy of intratympanic STR001 thermogel to preserve residual hearing in adults undergoing cochlear ... | ||
Medical condition: Prevention of Hearing Loss after Cochlear Implant Surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) ES (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-001646-10 | Sponsor Protocol Number: ANIMAL-523-2014-2569 | Start Date*: 2017-06-22 |
Sponsor Name:Uppsala University Hospital | ||
Full Title: Anesthesia Induced Hormonal Oliguria Trial | ||
Medical condition: Anaesthesia in adult patients undergoing general surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-004852-39 | Sponsor Protocol Number: ORTEGA-PHRCK-2017 | Start Date*: 2019-03-12 |
Sponsor Name:CHU Dijon Bourgogne | ||
Full Title: Benefit of a flash dose of corticosteroids in digestive surgical oncology: a randomized, double blind, placebo-controlled trial | ||
Medical condition: | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2022-003262-20 | Sponsor Protocol Number: PROPHYLOXITIN | Start Date*: 2023-02-23 |
Sponsor Name:CHU de Poitiers | ||
Full Title: Intermittent cefoxitin administration versus loading bolus followed by continuous infusion for the prevention of surgical site infection in colorectal surgery: a multicentre, double-blind, randomiz... | ||
Medical condition: colorectal surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003407-34 | Sponsor Protocol Number: pre-CIN | Start Date*: 2021-06-01 |
Sponsor Name:Oslo University Hospital | ||
Full Title: A randomized clinical three-arm trial comparing inflammation and cystoid macular edema for the medication regimens preoperative and postoperative topical NSAIDs to only postoperative topical NSAIDs... | ||
Medical condition: Cataract surgery, and the medical treatment is anti-inflammatory eye drops to treat (and prevent) intraocular inflammation and development og cystoid macular edema. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005534-19 | Sponsor Protocol Number: FRIA_FATSURG_1 | Start Date*: 2012-01-31 |
Sponsor Name:Vrije Universiteit Brussel | ||
Full Title: The effect of peri-operative anti-inflammatory treatment on postoperative muscle weakness and muscle fatigue in elderly elective surgery patients: a double blinded randomized placebo-controlled trial. | ||
Medical condition: Post-operative muscle weakness, fatigue and inflammation. | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-001252-41 | Sponsor Protocol Number: NA | Start Date*: 2022-07-08 |
Sponsor Name:CHU de Liège | ||
Full Title: Preventing postoperative anaemia in total knee arthroplasty and impact of intravenous iron supplementation on postoperative functional recovery : a randomized clinical trial | ||
Medical condition: Total Knee Arthroplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003300-14 | Sponsor Protocol Number: 74719 | Start Date*: 2020-10-07 |
Sponsor Name:Department of Cardiothoracic Surgery, Aalborg Universityhospital | ||
Full Title: Botulinum Toxin A as Treatment for Chronic Postsurgical Pain Following Lung Cancer Surgery: a Randomized Controlled Pilot Trial | ||
Medical condition: Post Thoracotomy Pain Syndrome (PTPS) | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2013-002217-36 | Sponsor Protocol Number: 20130021 | Start Date*: 2013-07-04 | ||||||||||||||||
Sponsor Name:Dept. of Anaesthesiology, Odense University Hospital | ||||||||||||||||||
Full Title: Crystalloid versus colloid for goal directed haemodynamic optimisation in major abdominal cancer surgery. | ||||||||||||||||||
Medical condition: Patients undergoing surgery for pancreatic, gastric or esophageal cancer. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-005701-43 | Sponsor Protocol Number: PROP-001-CP3 | Start Date*: 2013-04-11 | |||||||||||
Sponsor Name:Fresenius Kabi Deutschland GmbH | |||||||||||||
Full Title: Therapeutic Equivalence Study of Propofol Using Target-Controlled Infusion of Propofol 2% (20 mg/mL) MCT Fresenius Compared with Diprivan® 20 mg/mL (AstraZeneca) in Patients Undergoing Elective Sur... | |||||||||||||
Medical condition: Elective minor Surgery | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001124-31 | Sponsor Protocol Number: VDM 02/08 | Start Date*: 2008-04-11 |
Sponsor Name:UZ Leuven | ||
Full Title: Can the use of statin reduce the incidence of atrial flutter after major non-cardiac thoracic surgery ? A randomised double-blind study. | ||
Medical condition: Prevention of atrial flutter after major non-cardiac thoracic surgery. | ||
Disease: | ||
Population Age: | Gender: Male, Female | |
Trial protocol: BE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2019-002348-26 | Sponsor Protocol Number: HUS-PERFECT | Start Date*: 2020-02-18 |
Sponsor Name:Helsinki University Hospital | ||
Full Title: Role of delay and antibiotics on PERForation rate while waiting appendECTomy – Randomized non-inferiority trial (PERFECT) | ||
Medical condition: Acute appendicitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-005169-33 | Sponsor Protocol Number: CLEAN2 | Start Date*: 2018-02-23 | ||||||||||||||||
Sponsor Name:CHU DE POITIERS | ||||||||||||||||||
Full Title: An open label, multicenter, randomized trial of 2% chlorhexidine-70% isopropanol vs 5% povidone iodine-69% ethanol for skin antisepsis in reducing surgical-site infection after cardiac surgery | ||||||||||||||||||
Medical condition: surgery of the heart (valve, coronary or combined surgery) or of the aorta via a median sternotomy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004446-29 | Sponsor Protocol Number: LIBERAL-Trial | Start Date*: 2017-10-30 | |||||||||||
Sponsor Name:University Hospital Wuerzburg, Institution under public law, represented by the Medical Director | |||||||||||||
Full Title: Liberal transfusion strategy to prevent mortality and anaemia-associated, ischaemic events in elderly non-cardiac surgical patients | |||||||||||||
Medical condition: Elderly patients (>= 70 years) undergoing intermediate- or high-risk non-cardiac surgery | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005155-27 | Sponsor Protocol Number: KCT09/2015-SeptaNazal-Double | Start Date*: 2017-02-22 | |||||||||||
Sponsor Name:Krka, d.d., Novo mesto | |||||||||||||
Full Title: Comparison of the efficacy and safety of the fixed-dose combination of xylometazoline and dexpanthenol in SeptaNazal® and xylometazoline in nasal congestion in patients after surgery in the nose an... | |||||||||||||
Medical condition: Nasal congestion in patients after nasal surgery or nasal cavities surgery and in patients with acute rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SI (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019427-58 | Sponsor Protocol Number: 400-10-001 | Start Date*: 2010-09-08 | |||||||||||
Sponsor Name:Omrix Biopharmaceuticals Ltd | |||||||||||||
Full Title: A Phase III Randomized, Controlled, Superiority Study Evaluating the Fibrin Pad Versus Standard of Care Treatment in Controlling Parenchymal Bleeding During Elective Hepatic Surgery | |||||||||||||
Medical condition: Subjects undergoing elective, open, hepatic surgery during which a resection plane is created and wherein an appropriate Target Bleeding Site is identified. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005775-16 | Sponsor Protocol Number: SUBLIME1 | Start Date*: 2012-06-19 | |||||||||||
Sponsor Name:Research and Development Department | |||||||||||||
Full Title: A randomised, double blind, placebo-controlled trial of continuous subpectoral local anaesthetic infusion for pain and shoulder function following mastectomy. | |||||||||||||
Medical condition: Post-operative pain following mastectomy surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003638-10 | Sponsor Protocol Number: 2016_37 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:CHRU LILLE | |||||||||||||
Full Title: INTRANASAL CLONIDINE PREDICTION IN PEDIATRIC SURGERY: RANDOMIZED STUDY AGAINST PLACEBO | |||||||||||||
Medical condition: intra-nasal premedication instead of oral, intravenous or no premedication. | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
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