- Trials with a EudraCT protocol (74)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
74 result(s) found for: Epidural Anesthesia.
Displaying page 1 of 4.
EudraCT Number: 2010-021783-15 | Sponsor Protocol Number: Version 1.0 | Start Date*: 2010-12-31 | ||||||||||||||||
Sponsor Name:Guys and St Thomas' NHS Foundation Trust | ||||||||||||||||||
Full Title: Ropivacaine 0.75% versus Levobupivacaine 0.5% for conversion of labour epidural to surgical anaesthesia for emergency Caesarean section. (RoLe Trial) | ||||||||||||||||||
Medical condition: Conversion of labour epidural to surgical anaesthesia for emergency Caesarean section | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-001738-33 | Sponsor Protocol Number: I14032 | Start Date*: 2015-09-24 | |||||||||||
Sponsor Name:CHU de LIMOGES | |||||||||||||
Full Title: Programmed Intermittent Epidural Bolus versus Continuous Epidural Infusion for third trimester voluntary termination of pregnancy analgesia : a randomized study. | |||||||||||||
Medical condition: Termination Pregancy | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010594-20 | Sponsor Protocol Number: P 0901 | Start Date*: 2010-04-13 |
Sponsor Name:LUMC | ||
Full Title: Thoracic epidural anesthesia with ropivacaine: effects of age on neural blockade and cardiovascular parameters | ||
Medical condition: Medical conditions will not be investigated per se, however we will study the effect of standard thoracic epidural anesthesia on specific age groups undergoing lung surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-001176-37 | Sponsor Protocol Number: 07/S1401/27 | Start Date*: 2007-05-29 | |||||||||||||||||||||
Sponsor Name:NHS Tayside | |||||||||||||||||||||||
Full Title: A randomised, controlled trial to determine the median effective concentration of bupivacaine, levobupivacaine and ropivacaine after intrathecal and extradural injection for pain relief in the firs... | |||||||||||||||||||||||
Medical condition: Pain in early labour | |||||||||||||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-000202-75 | Sponsor Protocol Number: P.Sitsen.03 | Start Date*: 2007-06-15 |
Sponsor Name:Leids Universitair Medisch Centrum | ||
Full Title: A comparison of the efficacy of levobupivacaine 0,125%, ropivacaine 0,125% and ropivacaine 0,2%, all combined with sufentanil 0.5 micrograms/mL, in patient-controlled epidural analgesia after hyste... | ||
Medical condition: Primary Objective •to compare the analgesic efficacy of levobupivacaine and ropivacaine in patient-controlled epidural analgesia, as assessed by the number of requests for epidural bolus injections... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004313-82 | Sponsor Protocol Number: 30-09-2014 | Start Date*: 2015-02-03 |
Sponsor Name:Anaesthesia and Operative Services, Kuopio University Hospital | ||
Full Title: Efficacy and safety of epidural oxycodone | ||
Medical condition: Acute postoperative pain after gynaecologic surgery. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: FI (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000903-10 | Sponsor Protocol Number: 26022016 | Start Date*: 2017-01-04 |
Sponsor Name:Oulu University Hospital | ||
Full Title: Efficacy and blood concentrations of epidural hydromorphone in labour | ||
Medical condition: Labour pain | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FI (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000470-19 | Sponsor Protocol Number: CHUB-PD001 | Start Date*: 2014-04-17 |
Sponsor Name:Centre Hospitalier Universitaire Brugmann | ||
Full Title: comparative study between conventional epidural versus ambulatory epidural: effect during labor in pregnant women | ||
Medical condition: a single fetus pregnancy over 36 weeks and less than 42 weeks in adult nulliparous | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-004397-14 | Sponsor Protocol Number: 2015-2 | Start Date*: 2017-01-06 |
Sponsor Name:Akershus university hospital | ||
Full Title: THE PROGRAMMED INTERMITTENT EPIDURAL BOLUS ADRENALINE STUDY | ||
Medical condition: Vaginal labor/delivery | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NO (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-001349-41 | Sponsor Protocol Number: MD2012/1 | Start Date*: 2012-05-15 |
Sponsor Name:AZ Groeninge | ||
Full Title: Influence of dexamethasone on postoperative analgesia after combined spinal epidural for cesarean delivery. | ||
Medical condition: Postoperative pain | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000486-23 | Sponsor Protocol Number: #01/01.02.2016 | Start Date*: 2016-08-10 | |||||||||||
Sponsor Name:Helsinki University Central Hospital | |||||||||||||
Full Title: Spinal or epidural fentanyl or sufentanil for labour pain in early phase of the labour | |||||||||||||
Medical condition: Labour pain | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000889-35 | Sponsor Protocol Number: CHUB-PIB | Start Date*: 2016-05-26 |
Sponsor Name:Centre Hospitalier Universitaire Brugmann | ||
Full Title: Comparison of two methods of administration of the epidural, by programmed intermittent bolus or continuous perfusion, on the incidence of instrumented deliveries and cesareans in primiparous women. | ||
Medical condition: Fist child delivery with epidural | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-000298-20 | Sponsor Protocol Number: CHL.3/01-2016 | Start Date*: 2016-10-18 | |||||||||||
Sponsor Name:Sintetica S.A. | |||||||||||||
Full Title: Comparison of epidural Chloroprocaine 3% and Ropivacaine 0.75% for unplanned Caesarean section in labouring women who have an epidural catheter in situ | |||||||||||||
Medical condition: Local epidural anaesthesia in labouring women who have an epidural catheter in situ and established analgesia and need unplanned Caesarean | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) DE (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005424-33 | Sponsor Protocol Number: 17308 | Start Date*: 2008-02-06 |
Sponsor Name:Sint Lucas Andreas | ||
Full Title: Epidural analgesia versus Remifentanil PCA during labour | ||
Medical condition: To compare Remifentanil PCA with epidural anesthesia among healthy nulligravidia during labor. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-006632-67 | Sponsor Protocol Number: CHUBX2021/36 | Start Date*: 2022-03-14 | |||||||||||
Sponsor Name:CHU de Bordeaux | |||||||||||||
Full Title: Alkalinization of adrenalized lidocaine in extending epidural analgesia for extremely urgent cesarean section during labor: a randomized controlled trial. | |||||||||||||
Medical condition: epidural analgesia for extremely urgent cesarean | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005802-31 | Sponsor Protocol Number: PF2 | Start Date*: 2012-08-23 |
Sponsor Name:Consorci Mar Parc de Salut de Barcelona (Parc de Salut Mar) | ||
Full Title: Comparison of the analgesic efficacy of two different concentrations of epidural fentanyl (25mcg/ml and 8mcg/ml)to provide intraoperative analgesia. | ||
Medical condition: Management of Intraoperative pain during open colonic resection surgery comparing two different concentrations of epidural fentanyl. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001657-27 | Sponsor Protocol Number: -- | Start Date*: 2018-10-03 |
Sponsor Name: | ||
Full Title: Comparison of ultrasound guided Serratus Anterior Plane Block (SAPB) with continuous local anesthetic infusion and epidural analgesia in the treatment of multiple rib fracture analgesia: a prospect... | ||
Medical condition: Multiple traumatic rib fractures | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: FI (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001921-19 | Sponsor Protocol Number: BUSCAPART | Start Date*: 2014-02-11 | |||||||||||
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | |||||||||||||
Full Title: Randomised, masked, placebo-controlled study to evaluate the effects of a single intravenous dose of hyoscine bromide on the duration and pain in the latent and active labor | |||||||||||||
Medical condition: labor | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003319-76 | Sponsor Protocol Number: MVDV/ER082019 | Start Date*: 2019-10-09 |
Sponsor Name:Univerity Hospitals Leuven | ||
Full Title: High volume PCEA versus PIEB for labor analgesia: a randomized, double-blind multicenter non-inferiority study in nulliparous women. | ||
Medical condition: providing adequate analgesia during child birth | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-004918-22 | Sponsor Protocol Number: AGO/2015/011 | Start Date*: 2016-06-28 |
Sponsor Name:Ghent University Hospital | ||
Full Title: A comparison of chloroprocaine 3% versus levobupivacaine 0.5% for epidural anesthesia during caesarean section. | ||
Medical condition: anesthetics for women scheduled for elective caesarean section | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
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