- Trials with a EudraCT protocol (10)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
10 result(s) found for: Pneumoperitoneum.
Displaying page 1 of 1.
| EudraCT Number: 2018-001485-42 | Sponsor Protocol Number: NL65290.091.18 | Start Date*: 2018-06-14 |
| Sponsor Name:Radboudumc | ||
| Full Title: RECOVER study: the effect of low- versus normal pressure pneumoperitoneum during laparoscopic colorectal surgery on the early quality of recovery with perioperative care according to the enhanced r... | ||
| Medical condition: Laparoscopic colorectal surgery | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-001693-15 | Sponsor Protocol Number: IPPCollapse-II | Start Date*: 2016-08-08 |
| Sponsor Name:INSTITUTO DE INVESTIGACIÓN SANITARIA LA FE | ||
| Full Title: Individualized Pneumoperitoneum Pressure in Colorectal laparoscopic surgery versus standard therapy (IPPCollapse II) | ||
| Medical condition: Pneumoperitoneum Pressure in Colorectal laparoscopic surgery | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
| 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: 2017-003623-29 | Sponsor Protocol Number: 63227.091.17 | Start Date*: 2018-03-27 |
| Sponsor Name:Radboudumc | ||
| Full Title: MRI measurement of the effects of moderate versus deep neuromuscular blockade on the abdominal working space during laparoscopic surgery in a prospective cohort study. | ||
| Medical condition: We will investigate the effect of deep neuromuscular blockade on the abdominal working space. We will include patients undergoing laparoscopic surgery, including laparoscopic donor nephrectomy, lap... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-005502-29 | Sponsor Protocol Number: 2011-441 | Start Date*: 2012-01-12 | |||||||||||
| Sponsor Name:Mona R Gätke | |||||||||||||
| Full Title: Optimization of surgical conditions during laparoscopic cholecystectomy with deep or moderate neuromuscular blockade | |||||||||||||
| Medical condition: Surgical conditions during laparoscopic cholecystectomy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-002816-30 | Sponsor Protocol Number: 01072021 | Start Date*: 2021-11-12 | |||||||||||
| Sponsor Name:Department of Anaesthesiology, Aarhus University Hospital | |||||||||||||
| Full Title: Individualised perioperative blood pressure and fluid therapy in oesophagectomy - Study protocol for a prospective randomised controlled trial | |||||||||||||
| Medical condition: Oesophagectomy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-002924-99 | Sponsor Protocol Number: NL.58160.091.16 | Start Date*: 2016-10-27 |
| Sponsor Name:Radboudumc | ||
| Full Title: The effectiveness of deep versus moderate neuromuscular blockade during laparoscopic donor nephrectomy in enhancing postoperative recovery. | ||
| Medical condition: Live kidney donation is currently the most effect strategy to manage the shortage of donor kindeys for transplantation. Optimizing the safety and postoperative recovery after laparoscopic donornep... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| 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: 2016-002974-11 | Sponsor Protocol Number: IBU24h-EchoG | Start Date*: 2016-11-10 | |||||||||||
| Sponsor Name:María Carmen Bravo Laguna | |||||||||||||
| Full Title: Phase III, randomized, multicenter, double-blind clinical trial to evaluate two echo-guided administration regimens of ibuprofen in the treatment of patent ductus arteriosus: impact on intestinal p... | |||||||||||||
| Medical condition: patent ductus arteriosus | |||||||||||||
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| Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-003326-41 | Sponsor Protocol Number: 200719 | Start Date*: 2016-01-13 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
| Full Title: Randomized, Double-Blind, Multicenter, Phase III Study Comparing the Efficacy and Safety of Retosiban Versus Placebo for Women in Spontaneous Preterm Labor | |||||||||||||
| Medical condition: Preterm Labour | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
| Trial protocol: GB (Completed) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
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