- Trials with a EudraCT protocol (190)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (12)
190 result(s) found for: Epidural.
Displaying page 1 of 10.
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: 2009-011219-20 | Sponsor Protocol Number: 2009/04 | Start Date*: 2009-05-18 | |||||||||||
Sponsor Name:Hopital Foch | |||||||||||||
Full Title: Comparison between two methods of post-operative analgesia after thoracotomy: epidural administration of sufentanil and levobupivacaine and epidural administration of levobupivacaine associated wit... | |||||||||||||
Medical condition: postoperative epidural analgesia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000760-18 | Sponsor Protocol Number: 13.034 | Start Date*: 2014-11-24 |
Sponsor Name:Prof. Peter Licht | ||
Full Title: Supplementary Epidural Analgesia in Video-Assisted Thoracic Surgery (VATS) - The SEAVATS Study. | ||
Medical condition: Cancer pulmones | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2010-020020-21 | Sponsor Protocol Number: AN10/9307 | Start Date*: 2011-07-12 |
Sponsor Name:Leeds Teaching Hospitals Trust | ||
Full Title: Comparison of the ED95 dose of 0.075% and 0.1% bupivacaine for labour analgesia in primigravida | ||
Medical condition: Patients pregnant for the first time(primigravida)in early labour requesting epidural analgesia for pain relief. | ||
Disease: | ||
Population Age: Adults | 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: 2014-002036-14 | Sponsor Protocol Number: V3.10.5.2014 | Start Date*: 2014-08-08 | |||||||||||
Sponsor Name:Lars Bo Svendsen | |||||||||||||
Full Title: The effect of epidural anaesthesia on systemic and splanchnic hemodynamic during gastroesophageal resections, a randomized controlled trial | |||||||||||||
Medical condition: The effect of epidural anaesthesia on systemic and splanchnic hemodynamic during gastroesophageal cancer resection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000333-36 | Sponsor Protocol Number: 17012006 | Start Date*: 2006-04-26 |
Sponsor Name:Hull & East Yorkhire NHS Hospitals Trust | ||
Full Title: A randomised comparison of 0.5% levobupivacaine with a lidocaine/epinephrine/ fentanyl mixture for epidural top up for emergency caesarean section after “low dose” epidural for labour | ||
Medical condition: pregnant women, in labour requiring emergency caesarean section under epidural anaesthesia | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-003590-25 | Sponsor Protocol Number: NL | Start Date*: 2020-06-15 | |||||||||||
Sponsor Name: | |||||||||||||
Full Title: a Randomized controlled trial for epidural Analgesia for Pain relief after lumbar Interlaminar Decompressive spine surgery - RAPID | |||||||||||||
Medical condition: Lumbar spinal stenosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017665-31 | Sponsor Protocol Number: CSE | Start Date*: 2010-09-30 |
Sponsor Name:AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA` DI NOVARA | ||
Full Title: Effect on mother and fetus of epidural and combined spinal-epidural techniques for labour analgesia | ||
Medical condition: Labour | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: IT (Completed) | ||
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: 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 (Completed) | ||
Trial results: (No results available) |
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: 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: 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: 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: 2006-005845-12 | Sponsor Protocol Number: 11/2006 - MVdV | Start Date*: 2007-01-08 |
Sponsor Name:UZ leuven, Marc Van de Velde | ||
Full Title: Combined spinal-epidural anaesthesia during labour : has the epidural administration of clonidine and neostigmine a positive influence on the quality of analgesia ? | ||
Medical condition: combined spinal-epidural analgesia during labour | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
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 (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004696-24 | Sponsor Protocol Number: ANESBUPI_1/2014 | Start Date*: 2016-02-29 |
Sponsor Name:HOSPITAL UNIVERSITARIO LA PAZ, SERVICIO DE ANESTESIA | ||
Full Title: Breakthrough pain incidence in pregnant women comparing two Epidural analgesia shemes added to a continuous infusion (bowling planned indicators and analgesia epidural patient controlled): double-b... | ||
Medical condition: EPIDURAL ANALGESIA IN PARTURIENTS | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (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 |
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