- Trials with a EudraCT protocol (28)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
28 result(s) found for: Laparoscopic cholecystectomy.
Displaying page 1 of 2.
EudraCT Number: 2022-000904-36 | Sponsor Protocol Number: IBS-DOTIG-ECM-2202 | Start Date*: 2022-05-09 | |||||||||||
Sponsor Name:Instituto de Investigación Biomédica de Salamanca | |||||||||||||
Full Title: Randomized clinical trial to evaluate the dose and administration time of indocyanine green in near-infrared fluorescent cholangiography during laparoscopic cholecystectomy. | |||||||||||||
Medical condition: Laparoscopic cholecystectomy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: View results |
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: 2009-015236-15 | Sponsor Protocol Number: NILA/01/09 | Start Date*: 2010-01-22 |
Sponsor Name:Department of Surgery, National University of Ireland | ||
Full Title: NEBULISED INTRAPERITONEAL LOCAL ANAESTHETIC (NILA) FOR LAPAROSCOPIC SURGERY: A PROSPECTIVE, RANDOMISED, DOUBLE BLINDED, PLACEBO CONTROLLED CLINICAL TRIAL | ||
Medical condition: Post operative shoulder tip pain following laparoscopic appendectomy, cholecystectomy, laparoscopic Nissen fundoplication or diagnostic laparoscopy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-000043-10 | Sponsor Protocol Number: 200701 | Start Date*: 2007-01-30 | |||||||||||
Sponsor Name:Fakultní nemocnice Královské Vinohrady | |||||||||||||
Full Title: Combination of alpha2-adrenoreceptor agonists, opioids and ketamine for improving of perioperative course | |||||||||||||
Medical condition: Praeanaesthetic preparation (premedication) for patients scheduled for laparoscopic cholecystectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-018247-24 | Sponsor Protocol Number: AR HSG 01 2010 cholecysthectomy | Start Date*: 2010-03-04 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SAN GERARDO DI MONZA | |||||||||||||
Full Title: Peritoneal nebulization of Ropivacaine for postoperative pain control after laparoscopic cholecystectomy A multicentre, randomized, controlled, double blinded, phase III clinical trial; comparing... | |||||||||||||
Medical condition: Elective Laparoscopic cholecystectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002428-34 | Sponsor Protocol Number: ANE-DEX-2019 | Start Date*: 2019-09-27 | |||||||||||
Sponsor Name:HOSPITAL CLINICO SAN CARLOS | |||||||||||||
Full Title: ONE CENTRE, DOUBLE BLIND, ONE CENTRE, RANDOMIZED CLINICAL TRIAL, IN TWO PARALLEL GROUPS TO EVALUATE THE EFICACY IN THE PREVENTION OF POSTOPERATIVE NAUSEA AND VOMITING OF DEXAMETHASONE VERSUS METHIL... | |||||||||||||
Medical condition: Postoperative nausea and vomiting after not urgent laparoscopic cholecystectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007951-14 | Sponsor Protocol Number: 19.4.318 | Start Date*: 2008-05-05 |
Sponsor Name:NV Organon | ||
Full Title: A multi-center, randomized, parallel-group, comparative, active-controlled, safety-assessor blinded trial in adult subjects comparing the efficacy and safety of sugammadex administered at 1-2 PTC w... | ||
Medical condition: Not applicable | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) GB (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-002779-32 | Sponsor Protocol Number: PREEMTIVE | Start Date*: 2019-12-26 |
Sponsor Name:BERTA CASTELLANO PAULIS | ||
Full Title: “Pre-emptive analgesia with Ibuprofen in outpatient laparoscopic cholecystectomy. Recovery Quality ” | ||
Medical condition: AMBULATORY LAPAROSCOPIC COLECISTECTOMY | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004515-20 | Sponsor Protocol Number: PAIKIPAIN | Start Date*: 2015-12-31 | |||||||||||
Sponsor Name:Vesa Kontinen | |||||||||||||
Full Title: Targeted pain management based on patient specific risk assesment in ambulatory surgery | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2012-001886-33 | Sponsor Protocol Number: MK-8616-076-00 | Start Date*: 2012-10-30 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: Randomized, Controlled, Parallel Group, Double Blind Trial to Compare the Use of Deep or Standard Neuromuscular Blockade in Combination With Low or Standard Insufflation Pressures Using a 2x2 Fact... | |||||||||||||
Medical condition: Patients undergoing elective in-patient laparoscopic cholecystectomy procedures under general anesthesia with neuromuscular relaxation and active reversal of neuromuscular blockade | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) FI (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002029-36 | Sponsor Protocol Number: AR_HSG_ 02-2008 | Start Date*: 2008-04-24 | |||||||||||
Sponsor Name:A.O. SAN GERARDO DI MONZA | |||||||||||||
Full Title: Impact of intraperitonael nebulization of local anesthetic on postoperative pain associated with laparoscopic cholecystectomy | |||||||||||||
Medical condition: Intra and post operatorive period | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001364-30 | Sponsor Protocol Number: BBH-TQL-LC | Start Date*: 2013-07-22 | |||||||||||
Sponsor Name:Bispebjerg Hospital | |||||||||||||
Full Title: Ultrasoundguided transmuscular quadrates lumborum block after elective laparoscopic cholecystectomy. A prospective, randomised clinical trial. | |||||||||||||
Medical condition: Postoperative pain following laparoscopic cholecystectomy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000732-22 | Sponsor Protocol Number: OSTAP | Start Date*: 2020-05-18 |
Sponsor Name:Pablo Rama Maceiras | ||
Full Title: Effectiveness comparative study of oblique subcostal transversus abdominis plane block (OSTAP block) versus laparoscopic ports infiltration in patients undergoing elective cholecystectomy. | ||
Medical condition: Elective cholecystectomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-017420-75 | Sponsor Protocol Number: SM1-plp-09 | Start Date*: 2010-01-25 | ||||||||||||||||
Sponsor Name:Joergen B Dahl | ||||||||||||||||||
Full Title: Effekten af transversus abdominis plane (TAP) blok på patienter, der får foretaget laparoskopisk cholcystektomi i dagkirurgisk regi | ||||||||||||||||||
Medical condition: Postoperative pain in patients undergoing laparoscopic cholecystectomy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000164-93 | Sponsor Protocol Number: 1000000 | Start Date*: 2006-05-10 |
Sponsor Name:Department of Anesthesiology University Hospital Center | ||
Full Title: Effect of Nutritional Support on Liver Integrity during General Anesthesia for Laparoscopic Cholecystectomy. A Pilot Study | ||
Medical condition: To the best of our knowledge, there is no clinical study on the protective effect of nutritional support on the liver in the perioperative setting using clinical and biological variables. Regarding... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005135-15 | Sponsor Protocol Number: 8101 colloidAug08 | Start Date*: 2009-01-12 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:University of Nottingham | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Do 100 kiloDaltons matter? A prospective randomised double-blind study on the blood volume expanding effects of two different colloids in patients undergoing laparoscopic cholecystectomy | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Patients undergoing laparoscopic cholecystectomy | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-004878-29 | Sponsor Protocol Number: NA | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:St. Antonius Hospital | |||||||||||||
Full Title: Perioperative antibiotic use in the treatment of acute calculous cholecystitis | |||||||||||||
Medical condition: Acute calculous cholecystitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002085-39 | Sponsor Protocol Number: 2013-03-23 | Start Date*: 2013-07-09 | |||||||||||
Sponsor Name:Kuopio University Hospital | |||||||||||||
Full Title: Effect of dexketoprofen on analgesic concentration of oxycodone after laparoscopic cholecystectomy | |||||||||||||
Medical condition: Cholelithiasis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003566-26 | Sponsor Protocol Number: OXN4501 | Start Date*: 2009-02-27 | |||||||||||
Sponsor Name:Mundipharma GmbH | |||||||||||||
Full Title: An exploratory, randomised, parallel-group, open-label, multicentre study to assess the post-operative management of moderate to severe pain in patients who underwent laparoscopic cholecystectomy, ... | |||||||||||||
Medical condition: post-operative management of moderate to severe pain in patients who underwent laparoscopic cholecystectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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