- Trials with a EudraCT protocol (92)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
92 result(s) found for: Ambulatory surgery.
Displaying page 1 of 5.
EudraCT Number: 2019-003972-37 | Sponsor Protocol Number: CLVSPR19 | Start Date*: 2020-06-05 |
Sponsor Name:Hospital Arnau de Vilanova - Lliria | ||
Full Title: Comparative study of cloroprocaine versus prilocaine intrathecal anestesia in major ambulatory surgery | ||
Medical condition: Inguinal hernia liable to ambulatory surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001944-13 | Sponsor Protocol Number: ZAA15CPP | Start Date*: 2016-07-27 |
Sponsor Name:Zaans Medisch Centrum | ||
Full Title: Chloroprocaine vs prilocaine for spinal anaesthesia in day-case surgery: a double-blind randomized trial | ||
Medical condition: Patients scheduled for ambulatory knee arthroscopy surgery receive one of the two spinal anaesthetics | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001079-35 | Sponsor Protocol Number: PRPK | Start Date*: 2019-08-29 |
Sponsor Name:Cliniques universitaires Saint-Luc | ||
Full Title: A prospective randomized study in ambulatory patients undergoing upper limb bone surgery under single shot axillary plexus block. | ||
Medical condition: Do patients who are very painful when the axillary block wears off after bone surgery of the upper limb have a pre-existing central sensitization? Could this “rebound pain” be prevented by pre-inc... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-005949-19 | Sponsor Protocol Number: CCOX189A2427 | Start Date*: 2006-07-21 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A multicenter, randomized, double-blind, placebo controlled, parallel group study to compare efficacy of a single dose of lumiracoxib 400 mg given preemptively versus post-operatively, in reducing ... | ||
Medical condition: Ambulatory arthroscopic knee surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-007019-10 | Sponsor Protocol Number: AGO/2007/015 | Start Date*: 2008-01-21 |
Sponsor Name:University Hospital Ghent | ||
Full Title: Comparison of the therapeutic efficacy and side effects of tramadol per os (Tradonal Odis® orodispersible tablets) versus an optimised dosis of travenous tramadol for postoperative pain relief in a... | ||
Medical condition: Ambulatory surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003987-35 | Sponsor Protocol Number: Metamizole001 | Start Date*: 2015-11-10 |
Sponsor Name:JESSA Hospital | ||
Full Title: Metamizole versus NSAID at home after ambulatory surgery: a double-blind randomized controlled trial | ||
Medical condition: Pain after ambulatory surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-002901-30 | Sponsor Protocol Number: AGO/2006/006 | Start Date*: 2006-06-22 |
Sponsor Name:University Hospital Ghent | ||
Full Title: Tramadol iv. : influence of dose and dose intervals on therapeutic accuracy and side effects when used for postoperative pain relief in ambulatory surgery | ||
Medical condition: ASA I and II | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-002559-27 | Sponsor Protocol Number: 2017-03 | Start Date*: 2018-03-29 |
Sponsor Name:Zaans Medisch Centrum | ||
Full Title: ED50 and ED90 of intrathecal 1% chloroprocaine in day-case knee arthroscopy | ||
Medical condition: Patients scheduled for ambulatory knee arthroscopy surgery receive intrathecal chloroprocaine | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-005074-19 | Sponsor Protocol Number: BRIDION_ERASME | Start Date*: 2018-04-06 |
Sponsor Name:Erasme Hospital | ||
Full Title: Minimal optimal dose of Sugammadex during ambulatory surgery in dentistry | ||
Medical condition: women and men> 18 years of age Elective Surgery BMI <30, patients who gave consent to free and informed participation in writing to benefit from tooth extraction | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001305-82 | Sponsor Protocol Number: IC3627/18 | Start Date*: 2019-05-16 |
Sponsor Name:Laura Perelló Moreno | ||
Full Title: Study on the advantages of local post-operative infiltration in forefoot surgery. | ||
Medical condition: management of postoperative pain in ambulatory foot surgery that allows the realization of immediate rehabilitation and better functional results and personal satisfaction | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002399-25 | Sponsor Protocol Number: Sevo-Des-2015-01 | Start Date*: 2015-11-04 |
Sponsor Name:Servicio de Anestesia Infantil. Hospital Universitario La Paz | ||
Full Title: CLINICAL TRIAL TO COMPARE THE INCIDENCE AND CHARACTERISTICS OF POSTOPERATIVE AGITATION IN PEDIATRIC PATIENTS AFTER ANESTHESIA WITH SEVOFLURANE OR DESFLURANE IN AMBULATORY SURGERY. | ||
Medical condition: AGITATION AFTER POSTOPERATIVE ANESTHESIA IN PEDIATRIC PATIENTS | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-002890-31 | Sponsor Protocol Number: Pregab1 | Start Date*: 2006-08-25 |
Sponsor Name:Dept. of Anaesthesia, Medical University of Vienna | ||
Full Title: Does Pregabalin reduce preoperative anxiety: a placebo controlled study | ||
Medical condition: Patients should receive Pregabalin or placebo as premedication one hour before ambulatory elective surgery. After this they have to assess their anxiety and pain with Visual Analog Scale (VAS) for ... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-005026-35 | Sponsor Protocol Number: 35RC14_9853_DEXA-OP | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:Centre Hospitalier Universitaire de Rennes | ||||||||||||||||||
Full Title: Study DEXA-OP. Can the dexaméthasone replace the kétoprofène in the strategy of per-operating multimodal analgesia in pediatric ambulatory surgery? A double-blind randomized comparative study. | ||||||||||||||||||
Medical condition: Per-operating analgesia, pediatric ambulatory surgery | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001340-29 | Sponsor Protocol Number: IIBSP-LEV-2011-21 | Start Date*: 2011-09-16 |
Sponsor Name:Institut de Recerca del Hospital de la Santa Creu i Sant Pau | ||
Full Title: Effectiveness of Added blocking of radial and median nerves with levobupivacaine in the control of postoperative pain in the rhizarthrosis ambulatory surgery | ||
Medical condition: Rhizarthrosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-000905-22 | Sponsor Protocol Number: 5505 | Start Date*: 2013-07-09 | |||||||||||
Sponsor Name:Hôpitaux Universitaires de Strasbourg | |||||||||||||
Full Title: à compléter | |||||||||||||
Medical condition: akathisia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
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: 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: 2013-000384-87 | Sponsor Protocol Number: AGO/2013/001 | Start Date*: 2013-03-05 | |||||||||||
Sponsor Name:Ghent University Hospital | |||||||||||||
Full Title: Intraperitoneal atomization of levobupivacaine during gynecological laparoscopic procedures : Impact on pain, opioid use and length of recovery room stay (IPLA). | |||||||||||||
Medical condition: Patients who are planned for gynecological laparoscopic interventions on an ambulatory basis. | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
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: 2019-002801-23 | Sponsor Protocol Number: Metamizole002 | Start Date*: 2019-10-08 |
Sponsor Name:Jessa Hospital | ||
Full Title: Evaluation of the added value of Metamizole to standard post-operative treatment after ambulant surgery: a double-blind, randomized controlled trial | ||
Medical condition: Optimalization of post-operative treatment after ambulant surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
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