- Trials with a EudraCT protocol (43)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
43 result(s) found for: Hernia repair.
Displaying page 1 of 3.
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: 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: 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: 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: 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: 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: 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: 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) |
EudraCT Number: 2005-000538-19 | Sponsor Protocol Number: CLIN004-0009 | Start Date*: 2005-04-21 | |||||||||||
Sponsor Name:DURECT Corporation | |||||||||||||
Full Title: Protocol CLIN004−0009 (February 02, 2005): A Pharmacodynamic/Pharmacokinetic Study of SABER−Bupivacaine and/or Bupivacaine HCl Administered Intra−operatively During Open Inguinal Hernia Repair unde... | |||||||||||||
Medical condition: Inguinal hernia repair | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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: 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: 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: 2004-001789-42 | Sponsor Protocol Number: IC01/04/DKP | Start Date*: 2004-12-07 | |||||||||||
Sponsor Name:Laboratorios Menarini, S.A. | |||||||||||||
Full Title: A MULTICENTRE CLINICAL TRIAL EVALUATING THE ANALGESIC EFFICACY AND SAFETY OF DEXKETOPROFEN TROMETAMOL (50 mg i.v. FOLLOWED BY AN ORAL DOSAGE OF 25 mg t.i.d.) VERSUS METAMIZOL (2 g i.v. and 575 mg t... | |||||||||||||
Medical condition: Patients who underwent ambulatory surgery consisting in unilateral inguinal mesh hernioplasty | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004113-96 | Sponsor Protocol Number: AGO/2008/008 | Start Date*: 2008-09-17 |
Sponsor Name:University Hospital Ghent | ||
Full Title: DRainage versus sEAlant in prospective, Monocentric, double blinded randomized trial to evaluate the effect of fibrin glue in surgical repair of incisional hernias (DREAM-trial) | ||
Medical condition: Open incisional hernia mesh repair | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002880-33 | Sponsor Protocol Number: PINDEX | Start Date*: 2016-10-28 |
Sponsor Name:University of Turku | ||
Full Title: Bioavailability and pharmacokinetics of intranasal dexmedetomidine in children | ||
Medical condition: Paediatric patients scheduled for minor procedures such as intra-articular drug injections, hernia repair, bronchoscopy or magnetic resonance imaging. | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-015716-18 | Sponsor Protocol Number: AT08/09 | Start Date*: 2009-09-18 | |||||||||||
Sponsor Name:University Hospitals Leuven | |||||||||||||
Full Title: A comparative trial between the analgesic efficacy of a standard postoperative analgesic regimen and TAP- block in addition to a standard postoperative regimen after inguinal hernia repair in a su... | |||||||||||||
Medical condition: Pain treatment after laparascopic ingiunal hernia repair. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002595-82 | Sponsor Protocol Number: NL49853.094.14 | Start Date*: 2014-10-23 | |||||||||||
Sponsor Name:Westfriesgasthuis | |||||||||||||
Full Title: A randomised, double blind clinical trial comparison the effect of a ultrasound-guided transversus abdominis plane (TAP) block and wound infiltration on postoperative pain (48h) for open inguinal h... | |||||||||||||
Medical condition: Postoperative pain after hernia inguinalis repair surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006930-17 | Sponsor Protocol Number: 01/2006 | Start Date*: 2007-03-20 | ||||||||||||||||
Sponsor Name:HOSPITAL GENERAL DE VIC | ||||||||||||||||||
Full Title: ANESTESIA SUBARACNOIDEA SELECTIVA. COMPARACIÓN DE BUPIVACAINA HIPERBÁRICA CON PRILOCAINA HIPERBÁRICA PARA ARTROSCOPIA DE RODILLA O HERNIOPLASTIA INGUINAL EN CIRUGIA MAYOR AMBULATORIA | ||||||||||||||||||
Medical condition: Pacientes que se sometan a una artroplastia de rodilla ya sea diagnóstica o terapéutica y pacientes que se sometan a una hernioplastia inguinal | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003144-36 | Sponsor Protocol Number: NAC.TEP16 | Start Date*: 2020-11-18 |
Sponsor Name:Radboud University Medical Centre | ||
Full Title: Pilot study: postoperative pain reduction by pre emptive N-Acetylcysteine | ||
Medical condition: postoperative pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-000793-36 | Sponsor Protocol Number: HighNxGHR | Start Date*: 2015-04-28 | |||||||||||
Sponsor Name:Rigshospitalet, Copenhagen University Hospitals | |||||||||||||
Full Title: Effect of High-dose Target-controlled Naloxone Infusion on Pain and Hyperalgesia in Patients following Groin-Hernia-Repair. A companion study to: Pharmacokinetics of High-dose Target-controlled Nal... | |||||||||||||
Medical condition: Groin hernia repair | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
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