- Trials with a EudraCT protocol (33)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (33)
33 result(s) found for: Prilocaine.
Displaying page 1 of 2.
EudraCT Number: 2015-002744-14 | Sponsor Protocol Number: PRILPLEXUS1%-1.5% | Start Date*: 2015-12-23 |
Sponsor Name:Universitair Ziekenhuis Brussel | ||
Full Title: Comparative study with prilocaine 1% and prilocaine 1.5% for ultrasound guided axillary brachial plexus blockade | ||
Medical condition: - Onset of sensory and motor block - Quality and duration of the block - Influence of prilocaine on methemoglobinemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-004993-25 | Sponsor Protocol Number: LIDPR25VER | Start Date*: 2013-01-10 |
Sponsor Name:Verisfield (UK) Ltd | ||
Full Title: A multicenter, randomized, patient-blind, investigator-blind, placebo-controlled, crossover study of Lidocaine + Prilocaine/Verisfield (2.5+2.5)% w/w cream and EMLA/AstraZeneca cream, in patients u... | ||
Medical condition: Pain related to the cannulation of arteriovenous fistula cannulation in haemodialysis patients. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GR (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-003010-26 | Sponsor Protocol Number: B076201627677 | Start Date*: 2018-01-11 |
Sponsor Name:Centre Hospitalier Universitaire Saint Pierre , ULB | ||
Full Title: Hyperbaric Bupivacaine Versus Hyperbaric Prilocaine 2% for Cesarean Section Under Spinal Anesthesia: a Randomised and Controlled Clinical Trial | ||
Medical condition: Parturients undergoing an elective caesarean section performed under spinal anaesthesia | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2008-008177-57 | Sponsor Protocol Number: AN08/8748 | Start Date*: 2009-06-05 |
Sponsor Name:University of Leeds | ||
Full Title: “What is the ED95 dose of Prilocaine for femoral nerve block using ultrasound?” | ||
Medical condition: | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-000813-63 | Sponsor Protocol Number: TACs | Start Date*: 2016-04-06 |
Sponsor Name:Universitair Ziekenhuis Brussel | ||
Full Title: Comparative doubleblind study with prilocaine 2 % and 2-chloroprocaine for elective caesarean section. | ||
Medical condition: Healthy pregnant women undergoing a elective caesarean section with an uncomplicated pregnancy of a singleton, "full-term", all between 18-40 y (ASAI-II) through combined spinal and epidural approach. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001548-23 | Sponsor Protocol Number: 1 | Start Date*: 2020-04-02 | ||||||||||||||||
Sponsor Name:Guy's & St Thomas' NHS Foundation Trust | ||||||||||||||||||
Full Title: Does subarachnoid administration of hyperbaric prilocaine produce an improved recovery from anaesthesia when compared with hyperbaric bupivacaine when used to facilitate cervical cerclage in pregna... | ||||||||||||||||||
Medical condition: Cervical cerclage | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
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: 2018-000016-19 | Sponsor Protocol Number: PSCs | Start Date*: 2018-04-04 |
Sponsor Name:Universitair ziekenhuis Brussel | ||
Full Title: Randomized comparative double blind prospective study with hyperbaric prilocaine 2 % and 3 different doses of sufentanil for elective caesarean section. | ||
Medical condition: Healthy pregnant women | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Ongoing) | ||
Trial results: (No results available) |
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: 2015-005334-22 | Sponsor Protocol Number: 347PUNCIOHEMODIALISIS | Start Date*: 2016-05-31 |
Sponsor Name:HOSPITAL DE PALAMÓS | ||
Full Title: CLINICAL TRIAL FOR THE TREATMENT OF PAIN IN HEMODIALYSIS PUNCTURE WITH LIDOCAINE / PRILOCAINE, VERSUS CHLOROETHYL, CROSSOVER RANDOMIZED STUDY | ||
Medical condition: Hemodialysis is the most commonly used therapy for renal replacement being the arteriovenous fistula used for vascular access . Venipuncture in patients causes stress, pain and anxiety. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-002179-12 | Sponsor Protocol Number: PRILODE50-FUSION | Start Date*: 2022-09-16 | |||||||||||
Sponsor Name:Matilde Zaballos | |||||||||||||
Full Title: Determination of the effective dose 50 of intrathecal hyperbaric prilocaine required for the transrectal ultrasound guidance fusion-targeted prostate biopsy in ambulatory surgery | |||||||||||||
Medical condition: anaesthesia for prostate fusion biopsy in outpatient surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003650-15 | Sponsor Protocol Number: PSD502-PE-005 | Start Date*: 2008-12-29 | |||||||||||
Sponsor Name:Plethora Solutions Ltd | |||||||||||||
Full Title: A Phase II, multi-centre, double-blind, randomised, placebo-controlled, 4-way cross-over, dose-range finding study to evaluate efficacy and safety and tolerability of PSD502 in subjects with premat... | |||||||||||||
Medical condition: Premature Ejaculation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003610-86 | Sponsor Protocol Number: EMCD1403 | Start Date*: 2014-11-14 |
Sponsor Name: | ||
Full Title: A double blind randomized controlled trial comparing the efficacy of 7% lidocaine / 7% tetracaine cream versus 2,5% lidocaine / 2,5% prilocaine cream for local anaesthesia during laser treatment of... | ||
Medical condition: Pain during laser treatment of: 1. Tattoo 2. Acne keloidalis nuchae | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005240-93 | Sponsor Protocol Number: 1.3_amendment patientantal | Start Date*: 2007-03-13 |
Sponsor Name:Karolinska University Hospital | ||
Full Title: The effect of localanastetic when the drainage is removed, including women operated for breast cancer. [Svensk titel: effekt av lokalbedövning vid dränage borttagning]. | ||
Medical condition: Patients undergoin surgery for breast cancer, according to DSMIV. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002264-25 | Sponsor Protocol Number: | Start Date*: 2011-10-12 |
Sponsor Name:Medizinische Universität Wien,Univ.Klinik f.Anästhesie,Allgemeine Intensivmedizin u.Schmerztherapie | ||
Full Title: Cooling for reducing treatment-related pain when applying capsaicin 8% patch | ||
Medical condition: healthy volunteers | ||
Disease: | ||
Population Age: | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-002921-39 | Sponsor Protocol Number: 9859 | Start Date*: 2017-12-11 |
Sponsor Name:University hospital of Montpellier | ||
Full Title: Comparison of motor blockade duration in the context of scheduled caesarean section with spinal anaesthesia : hyperbaric Prilocaïne versus hyperbaric Bupivacaïne. | ||
Medical condition: Caesarean section anaesthesia | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000882-29 | Sponsor Protocol Number: 001 | Start Date*: 2016-02-18 | |||||||||||
Sponsor Name:Reinier de Graaf Groep | |||||||||||||
Full Title: Spinal hyperbaric Prilocaine 2% 60 or 80 mg: a dosing study in day care patients. | |||||||||||||
Medical condition: spinal anesthesia for open inguinal hernia repair or lower limb surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002397-12 | Sponsor Protocol Number: 2016-011-M | Start Date*: 2016-08-11 |
Sponsor Name:Reinier de Graaf Groep | ||
Full Title: Median Local Anaesthetic dose (MLAD) of Intrathecal Prilocaïne in total hip arthroplasty with the anterior approach. | ||
Medical condition: Spinal anesthesia during total hip arthroplasty with anterior approach | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005006-31 | Sponsor Protocol Number: EML053774_002 | Start Date*: 2007-04-03 |
Sponsor Name:Merck Sante France | ||
Full Title: A randomized, stratified on age, parallel group design study to investigate the safety, tolerability and pharmacokinetics after a 60 minutes application of 4% lidocaine cream compared to EMLA® crea... | ||
Medical condition: Topical anesthesia of healthy skin before venous or subcutaneous puncture, before superficial cutaneous instrumental surgery or laser beam (tattoo or cutaneousangioma) | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004652-13 | Sponsor Protocol Number: PSD502-PM-001 | Start Date*: 2006-02-01 |
Sponsor Name:PLETHORA SOLUTIONS LIMITED | ||
Full Title: Phase II, multi centre, randomised, double blind, placebo controlled, pilot study to determine efficacy, safety, tolerability and preliminary pharmacokinetics of PSD502 in the management of pain fr... | ||
Medical condition: management of pain from donor sites in burns subjects undergoing skin grafts | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
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