- Trials with a EudraCT protocol (198)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
198 result(s) found for: Laparoscopic surgery.
Displaying page 1 of 10.
EudraCT Number: 2021-001503-33 | Sponsor Protocol Number: 2019PI200 | Start Date*: 2021-07-21 | |||||||||||
Sponsor Name:CHRU de Nancy | |||||||||||||
Full Title: The impact of deep versus standard muscle relaxation on intra-operative safety during laparoscopic surgery: a multicenter strategy study – EURO RELAX STUDY | |||||||||||||
Medical condition: Intra-operative adverse events during laparoscopic surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
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: 2013-001167-22 | Sponsor Protocol Number: 43488 | Start Date*: 2017-06-29 |
Sponsor Name: | ||
Full Title: Spinal Morphine in laparoscopic gastro-intestinal surgery | ||
Medical condition: Patients with indications for laparoscopic gastro-intestinal surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-004098-17 | Sponsor Protocol Number: 35195 | Start Date*: 2009-03-31 |
Sponsor Name:East Tallinn Central Hospital | ||
Full Title: Double-Blind, Randomized, Placebo -Controlled Study to Evaluate the Efficacy of Pre-operative Administration of Etoricoxib 120 mg, Etoricoxib 120 mg and Paracetamol 1 g Combination or Placebo in th... | ||
Medical condition: Pre-operative Administration of Etoricoxib 120 mg, Etoricoxib 120 mg and Paracetamol 1 g Combination or Placebo in the Treatment of Postoperative Pain in Patients Undergoing Gynaecologic Laparoscop... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: EE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2016-005246-31 | Sponsor Protocol Number: ANEST01 | Start Date*: 2017-03-20 |
Sponsor Name:Complexo Hospitalario Universitario de Pontevedra | ||
Full Title: Analgesic effectiveness of ultrasound-guided bilateral Transversus Abdominis Plane (TAP) block technique for laparoscopic radical prostatectomy: a prospective, randomized, simple-blind study | ||
Medical condition: Patients scheduled for elective laparoscopic radical prostatectomy surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002309-39 | Sponsor Protocol Number: 60/2011 | Start Date*: 2016-07-08 |
Sponsor Name:Osakidetza | ||
Full Title: EFFECTIVENESS OF ROPIVACAINE 0.1% INTRAPERITONEAL IN POSTOPERATIVE PAIN CONTROL IN GYNECOLOGIC LAPAROSCOPIC SURGERY " | ||
Medical condition: EFECTIVENESS OF ROPIVACAINE 0,1% FOR PAIN CONTROL AFTER LAPAROSCOPIC GYNECOLOGICAL SURGERY | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-005090-20 | Sponsor Protocol Number: FADOI.01.2016 | Start Date*: 2018-05-17 | ||||||||||||||||
Sponsor Name:FONDAZIONE FADOI | ||||||||||||||||||
Full Title: Rivaroxaban or placebo for extended antithrombotic prophylaxis after laparoscopic surgery for colorectal cancer: a randomized, double blind, placebo-controlled study. THE PRO-LAPS STUDY II | ||||||||||||||||||
Medical condition: Prevention of venous thromboembolism after laparoscopic surgery for colorectal cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004273-88 | Sponsor Protocol Number: ASK-1-2011 | Start Date*: 2011-09-21 | |||||||||||
Sponsor Name:Erling Bjerregaard Pedersen, Medicinsk forskningsafsnit, Regionshospitalet Holstebro | |||||||||||||
Full Title: Effect of hydroxyethyl starch on renal handling of sodium and water, vasoactive hormones,biomarkers and the circulatory system in patients undergoing laparoscopic nephrectomy | |||||||||||||
Medical condition: Patients undergoing laparoscopic nefrectomy in generel anesthesia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002304-40 | Sponsor Protocol Number: SC05-2019 | Start Date*: 2019-09-17 |
Sponsor Name:University Hospitals Leuven | ||
Full Title: Transmuscular Quadratus lumborum block (TQL) for laparoscopic colorectal surgery: A multi-center, double blind, prospective randomized placebo-controlled trial. | ||
Medical condition: postoperative pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-003033-42 | Sponsor Protocol Number: EURO-RELAX | Start Date*: 2020-01-28 |
Sponsor Name:INSTITUTO DE INVESTIGACIÓN SANITARIA LA FE | ||
Full Title: The impact of deep versus standard muscle relaxation on intra-operative safety during laparoscopic surgery: a multicenter strategy study – EURO RELAX STUDY | ||
Medical condition: Intra-operative adverse events during laparoscopic surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-021604-16 | Sponsor Protocol Number: etoricoxib-fast-track-2010 | Start Date*: 2010-12-08 | |||||||||||
Sponsor Name:Charité Universitätsmedizin Berlin | |||||||||||||
Full Title: A double-blind, randomized, placebo controlled study to evaluate the effectiveness of etoricoxib as an additive analgesic to epidural analgesia in colon or rectum fast-track surgery | |||||||||||||
Medical condition: Post-operative pain after laparoscopic colon or rectum surgery in fast-track design | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005928-13 | Sponsor Protocol Number: 52/2005 | Start Date*: Information not available in EudraCT |
Sponsor Name:Landspitali-University Hospital | ||
Full Title: Prospective randomized double blind trial on the use of Scopoderm patch for control of post-operative nausea and vomitting in patients undergoing gynecologic laparoscopic procedures. | ||
Medical condition: Post-operative nausea and vomiting in patients undergoing gynecologic laparoscopic procedures. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: IS (Completed) | ||
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: 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: 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: 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: 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: 2010-019830-29 | Sponsor Protocol Number: 3621 | Start Date*: 2011-04-19 | |||||||||||
Sponsor Name:Hopitaux Universitaires de Strasbourg | |||||||||||||
Full Title: Evaluation of the effects of CO2 insufflation on central body temperature and on postoperative pain in laparoscopic surgery | |||||||||||||
Medical condition: Elective videolaparoscopic hysterectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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) |
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