- Trials with a EudraCT protocol (85)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (10)
85 result(s) found for: Hernia.
Displaying page 1 of 5.
EudraCT Number: 2007-006707-21 | Sponsor Protocol Number: arti2008 | Start Date*: 2008-01-30 | |||||||||||
Sponsor Name:Martina Bachmann | |||||||||||||
Full Title: Päiväkirurginen spinaalipuudutus artikaiinilla verrattuna bupivakaiini-fentanyyliin | |||||||||||||
Medical condition: Päiväkirurgiaan tuleva potilas, jolla on kirurgin arvioima tarve nivustyräleikkauksesta | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011322-34 | Sponsor Protocol Number: 0000 | Start Date*: 2009-06-25 | |||||||||||
Sponsor Name:Martina Bachmann | |||||||||||||
Full Title: Päiväkirurginen spinaalipuudutus artikaiinilla verrattuna artikaiini-fentanyyliin | |||||||||||||
Medical condition: Päiväkirurgiaan tuleva potilas, jolla on kirurgin arvioima tarve nivustyräleikkauksesta | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004522-85 | Sponsor Protocol Number: 4271055 | Start Date*: 2006-05-30 | |||||||||||
Sponsor Name:Hyks | |||||||||||||
Full Title: Paravertebraalipuudutuksen merkitys päiväkirurgisten potilaiden spinaalipuudutuksessa tehdyn nivustyräleikkauksen jälkeiseen kipuun | |||||||||||||
Medical condition: nivustyräleikkauksen jälkeinen postoperatiivinen kipu | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002878-35 | Sponsor Protocol Number: GAS study | Start Date*: 2008-07-15 | |||||||||||
Sponsor Name:ISTITUTO GIANNINA GASLINI | |||||||||||||
Full Title: The GAS study. A multi-site RCT comparing regional and general anaesthesia for effects on neurodevelopmental outcome and apnoea in infants | |||||||||||||
Medical condition: Inguinal Hernia | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011856-23 | Sponsor Protocol Number: ERNPL | Start Date*: 2009-09-16 | |||||||||||
Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | |||||||||||||
Full Title: Evaluation of acute postsurgery pain management in patients who undergo inguen hernia surgery | |||||||||||||
Medical condition: Acute post surgery pain in patients who undergo inguen hernia surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004916-39 | Sponsor Protocol Number: 2015-806 | Start Date*: 2016-01-19 | |||||||||||
Sponsor Name:Digestive Disease Center, Bispebjerg Hospital | |||||||||||||
Full Title: PreOperative Steroid in Abdominal Wall Reconstruction: A Double-blinded Randomized Clinical Trial | |||||||||||||
Medical condition: Patients who undergo abdominal wall reconstruction for repair of a giant ventral hernia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005494-21 | Sponsor Protocol Number: MARIA | Start Date*: 2006-11-23 | |||||||||||
Sponsor Name:HYKS Marian sairaala | |||||||||||||
Full Title: Hyperbaarisen artikaiini-glukoosiliuoksen ja pelkän artikaiinin vertailu spinaalipuudutuksessa nivustyräpotilailla | |||||||||||||
Medical condition: nivustyrä | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021851-23 | Sponsor Protocol Number: ARHSG032010 | Start Date*: 2011-04-19 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA S. GERARDO DI MONZA | |||||||||||||
Full Title: analgesic effectiveness of ultrasound-guided ilioinguinal iliohypogastric and genitofemoral nerve block after inguinal herniorrhaphy | |||||||||||||
Medical condition: Inguinal hernia elective surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019899-77 | Sponsor Protocol Number: dx3 | Start Date*: 2010-06-21 | ||||||||||||||||||||||||||
Sponsor Name:Mette Astrup Madsen | ||||||||||||||||||||||||||||
Full Title: Can preoperative Dexamethasone optimise surgical outcomes after laparoscopic inguinal hernia repair. | ||||||||||||||||||||||||||||
Medical condition: Postoperative pain, nausea, vomiting, general well-being and convalescence after laparoscopic groin hernia repair. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002802-19 | Sponsor Protocol Number: NMBDKHernia2014 | Start Date*: 2014-09-19 | |||||||||||
Sponsor Name:Department of Anaesthesiology | |||||||||||||
Full Title: Optimizing surgical conditions during laparoscopic umbilical, incisional –and linea alba herniotomy with deep neuromuscular blockade (The hernia study) | |||||||||||||
Medical condition: The purpose of this study is to investigate surgical work space and surgical conditions in patients scheduled for laparoscopic umbilical, -linea alba and incisional herniotomy. The patients will ac... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002741-39 | Sponsor Protocol Number: TIMELI001 | Start Date*: 2005-12-07 | |||||||||||
Sponsor Name:Prof. Giampiero CAMPANELLI | |||||||||||||
Full Title: A prospective, controlled, randomized, patient and evaluator blinded study to evaluate pain and further disabling complications in patients undergoing Lichtenstein technique for primary inguinal he... | |||||||||||||
Medical condition: Unilateral, uncomplicated primary inguinal hernia repair | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) ES (Completed) DK (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018403-29 | Sponsor Protocol Number: SM1-plp-10 | Start Date*: 2010-03-01 | |||||||||||
Sponsor Name:Jørgen B. Dahl | |||||||||||||
Full Title: Effekten af Transversus abdominis plane (TAP) block versus sårinfiltration versus placebo på patienter, der får foretaget åben operation for lyskebrok i dagkirurgisk regi | |||||||||||||
Medical condition: Inguinal hernia repair | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006295-37 | Sponsor Protocol Number: 06/AN/04 | Start Date*: 2007-04-05 | |||||||||||
Sponsor Name:NHS Greater Glasgow & Clyde | |||||||||||||
Full Title: A multi-site RCT comparing regional and general anaesthesia for effects on neurodevelopmental outcome and apnoea in infants. | |||||||||||||
Medical condition: Inguinal hernia in neonates and infants | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005469-58 | Sponsor Protocol Number: AGO/2014/007 | Start Date*: 2015-01-14 | |||||||||||
Sponsor Name:Ghent University Hospital | |||||||||||||
Full Title: Determination of the minimum local anesthetic dose (MLAD) of spinal chloroprocaine for inguinal herniorrhaphy in ambulatory surgery. | |||||||||||||
Medical condition: Inguinal herniorrhaphy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002945-41 | Sponsor Protocol Number: 78464317 | Start Date*: 2020-09-24 | ||||||||||||||||||||||||||
Sponsor Name:Lone Nikolajsen | ||||||||||||||||||||||||||||
Full Title: The use of intraoperative methadone in children undergoing open urological surgery | ||||||||||||||||||||||||||||
Medical condition: Postoperative pain in children undergoing open urological surgery | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male | |||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-013080-19 | Sponsor Protocol Number: 27538 | Start Date*: 2010-03-31 | |||||||||||||||||||||||||||||||
Sponsor Name:AMC | |||||||||||||||||||||||||||||||||
Full Title: Prokinetics to alter the position of the gastric acid pocket in Gastro Esophageal Reflux Disease | |||||||||||||||||||||||||||||||||
Medical condition: gastro-esophageal reflux disease (GERD) | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001860-45 | Sponsor Protocol Number: hospitalplato1 | Start Date*: 2020-01-14 |
Sponsor Name:Hospital Plató | ||
Full Title: Impact of topical antibiotic prophylaxis with Gentamicin on SSI rate on elective incisional hernia surgery: a randomised clinical trial. | ||
Medical condition: Surgical site infection on incisional hernia remains still high (8-14%). Its apperance is related to long and costfull treatments (daily cures, antibiotics and hospital readmission) and it is also ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-004670-88 | Sponsor Protocol Number: 4975-2-007-2 | Start Date*: 2005-05-23 | |||||||||||
Sponsor Name:AlgoRx Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Analgesic Efficacy, Safety and Tolerability of ALGRX 4975 in Subjects after Inguinal Hernia Repair | |||||||||||||
Medical condition: Inguinal Hernia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004280-30 | Sponsor Protocol Number: 20031209-2 | Start Date*: 2004-12-30 |
Sponsor Name:Landstinget Dalarna | ||
Full Title: Injestion of the steroid betamethasone during operation for inguinal hernia repair for purpose to optimize treatment of postoperative pain, reduction of postoperative discomfort like nausea and pos... | ||
Medical condition: Betamethasone will be studied for treatment of postoperative pain and discomfort after operations for inguinal hernia. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-002342-35 | Sponsor Protocol Number: SKY0402-C-201 | Start Date*: 2005-04-20 | |||||||||||
Sponsor Name:SkyePharma, Inc. | |||||||||||||
Full Title: A Phase 2, Multicenter, Randomized, Double-Blind, Dose-Escalating/De-Escalating Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of a Single Dose of Sustained-Release Encapsulated Bupiv... | |||||||||||||
Medical condition: Pain following inguinal hernia repair | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
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