- Trials with a EudraCT protocol (11)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
11 result(s) found for: Incisional hernia.
Displaying page 1 of 1.
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: 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: 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: 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: 2019-002240-24 | Sponsor Protocol Number: SIMASPK01b | Start Date*: 2019-06-27 |
Sponsor Name:Institut klinické a experimentální medicíny | ||
Full Title: The evolution of advanced microangiopathic diabetic complications before and after simultaneous pancreas and kidney transplantation evaluated with progressive non-invasive methods | ||
Medical condition: Surgical complications (hernia) after simultaneous pancreas and kidney transplantation | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: CZ (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001164-29 | Sponsor Protocol Number: NMBDK2013 | Start Date*: 2013-05-15 | ||||||||||||||||
Sponsor Name:Department of anesthesiology | ||||||||||||||||||
Full Title: Optimizing surgical conditions: Intraabdominal distance during gynecologic laparoscopic surgery with and without muscle relaxation (The measurement study) | ||||||||||||||||||
Medical condition: To investigate if deep neuromucular blockade improves intraabdominal volume compared to no neuromuscular blockade in patients scheduled for gynecologic laparoscopic surgery with pneumoperitoneum 12... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001155-22 | Sponsor Protocol Number: Lap2014NMB | Start Date*: 2014-05-22 | ||||||||||||||||
Sponsor Name:Mona Ring Gätke | ||||||||||||||||||
Full Title: Muscle relaxation during open upper abdominal surgery -can the surgical conditions be optimized? (The laparotomy study) | ||||||||||||||||||
Medical condition: The aim of the study is to investigate if intense NMB improves surgical conditions during operation in patients scheduled for elective open upper abdominal surgery. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-003502-28 | Sponsor Protocol Number: AP-325.04 | Start Date*: 2020-02-14 | |||||||||||
Sponsor Name:Algiax Pharmaceuticals GmbH | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo Controlled, Parallel Group Study to Evaluate the Efficacy and Safety of AP-325 in Subjects with Peripheral Post-surgical Neuropathic Pain | |||||||||||||
Medical condition: Peripheral post-surgical neuropathic pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002286-40 | Sponsor Protocol Number: 1-1 | Start Date*: 2006-12-05 | |||||||||||
Sponsor Name:Pfizer bv | |||||||||||||
Full Title: Chronic Pain Management after Herniorraphy Pregabaline versus Placebo | |||||||||||||
Medical condition: Patients suffering from chronic pain of neuropathic character after open hernia repair. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002866-19 | Sponsor Protocol Number: CRAD001AIT25 | Start Date*: 2011-07-25 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: A 3-month, multicenter, randomized, open label study to evaluate the impact of early vs delayed introductioN of EVERolimus on WOUND healing in de novo kidney transplant recipients (NEVERWOUND study) | |||||||||||||
Medical condition: Renal transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000796-32 | Sponsor Protocol Number: 185/13 | Start Date*: 2014-01-28 | |||||||||||
Sponsor Name:Policlinico A. Gemelli | |||||||||||||
Full Title: A multiple centre, randomised, open label, prospective clinical study to compare the efficacy and safety of a combination of tacrolimus with everolimus versus the combination of tacrolimus with MM... | |||||||||||||
Medical condition: KIDNEY TRANSPLANTATION | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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