- Trials with a EudraCT protocol (16)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (14)
16 result(s) found for: Articaine.
Displaying page 1 of 1.
EudraCT Number: 2006-006617-32 | Sponsor Protocol Number: 06/Q0605/1 | Start Date*: 2007-05-02 |
Sponsor Name:Kings College Hospital Trust R&D | ||
Full Title: A prospective randomised double blind parallel trial comparing Articaine versus Lignocaine for mandibular dentistry | ||
Medical condition: necessary dental surgery | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-000996-18 | Sponsor Protocol Number: FJQ-BUP-2014-01 | Start Date*: 2015-04-23 |
Sponsor Name:Complejo Hospitalario Torrecárdenas | ||
Full Title: CLINICAL TRIAL TO EVALUATE THE EFFICACY AND THE SECURITY OF DEXAMETASONE+BUPIBACAINE+ARTICAINE+EPINEFRINE “VERSUS” ARTICAINE+EPINEFRINE IN THE POSTQUIRURGICAL PAIN OF THIRD MOLAR SURGERY | ||
Medical condition: THIRD MOLAR REMOVING | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004307-20 | Sponsor Protocol Number: | Start Date*: 2012-02-09 | ||||||||||||||||
Sponsor Name:Reino Pöyhiä | ||||||||||||||||||
Full Title: Comparison of periosteal and subcutaneous infusions of articaine and bupivacaine in treatment of acute pain after sternotomy | ||||||||||||||||||
Medical condition: Patients undergoing elective open aortic or mitral valve, atrial septal defect or myxoma surgery | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002042-11 | Sponsor Protocol Number: 3699 | Start Date*: 2006-07-31 |
Sponsor Name:Newcastle Upon Tyne Hospitals NHS Trust | ||
Full Title: “The efficacy of inferior alveolar nerve block and buccal infiltration for pulp anaesthesia in mandibular teeth” | ||
Medical condition: N/A. This work is of direct relevance to everyday general dental practice. The outcomes of this work are likely to influence the way in which paractitioners approach the problem of anaesthetising m... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-004711-23 | Sponsor Protocol Number: DT11/9936 | Start Date*: 2013-05-22 |
Sponsor Name:Leeds Dental Institute | ||
Full Title: Comparative studies of the anaesthetic efficacy of 4% Articaine used as mandibular infiltration versus 2% Lidocaine used as inferior dental nerve block, in extraction and pulpotomy of mandibular pr... | ||
Medical condition: Dental caries in primary molars | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005528-13 | Sponsor Protocol Number: 30112012 | Start Date*: 2014-06-17 | |||||||||||
Sponsor Name:Helsinki University Hospital | |||||||||||||
Full Title: Comparison of Novel Articaine Lozenge Versus Placebo for Upper Gastrointestinal Endoscopy in Adults. A Randomized Double-blinded Controlled Study | |||||||||||||
Medical condition: Patients who undergo esophagogastroduodenoscopy procedure for a first time | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011618-12 | Sponsor Protocol Number: a002c | Start Date*: 2009-06-18 | |||||||||||
Sponsor Name:Helsinki Central university Hospital | |||||||||||||
Full Title: Pharyngeal anaestesia with articaine:does it reduce surgical stress in gastroscopy? | |||||||||||||
Medical condition: Pharyngeal anesthesia for gastroscopy | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000062-35 | Sponsor Protocol Number: ThereIsNoSponsorInvolved | Start Date*: 2011-04-05 | |||||||||||
Sponsor Name:Mikko Pitkänen, MD, PhD | |||||||||||||
Full Title: Artikaiini 40mg ja kloroprokaiini 40 mg päiväkirurgisina spinaalipuudutteina (Lyhenne: A40C40) | |||||||||||||
Medical condition: Knee arthroscopy performed as day case surgery | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001988-12 | Sponsor Protocol Number: 1.2000 | Start Date*: 2015-02-02 |
Sponsor Name:Academic Medical Center, Amsterdam | ||
Full Title: Fractional CO2 laser assisted delivery of topical articaine and epinephrine solution vs. topical EMLA administration: a randomized controlled pilot study | ||
Medical condition: local anesthesia of the skin prior to laser therapy of acne and traumatic scars | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-005202-19 | Sponsor Protocol Number: DyMZIS-01 | Start Date*: 2017-09-07 |
Sponsor Name:Chemische Fabrik Kreussler & Co. GmbH | ||
Full Title: Multicenter, randomized, split-mouth study to evaluate the acceptance and preference of lidocaine gel compared to injection anesthesia after non surgical periodontal treatment | ||
Medical condition: Moderate parodontitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-003552-29 | Sponsor Protocol Number: There is no commercial sponsor | Start Date*: 2008-09-12 | |||||||||||
Sponsor Name:Johannes Förster, anest.lääkäri | |||||||||||||
Full Title: Kloroprokaiini (40 mg) ja artikaiini (60 mg) päiväkirurgisina spinaalipuudutteina (Lyhenne: C40A60) | |||||||||||||
Medical condition: Verrataan 40 mg klooriprokaiinia (Ryhmä C40) ja 60 mg artikaiinia (Ryhmä A60) potilailla, joille on tarkoitus tehdä spinaalipuudutuksessa polven tähystys päiväkirurgisena toimenpiteenä. Hypoteesina... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001816-20 | Sponsor Protocol Number: 1.1000 | Start Date*: 2014-08-28 |
Sponsor Name:Academic Medical Center, Amsterdam | ||
Full Title: Fractional CO2 laser assisted delivery of topical anesthetics: a randomized controlled pilot study | ||
Medical condition: local anesthesia of the skin prior to minor cutaneous surgical procedures | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005195-40 | Sponsor Protocol Number: 61255762 | Start Date*: 2006-11-06 | |||||||||||
Sponsor Name:Leila Niemi-Murola | |||||||||||||
Full Title: Comparsion between articaine and lignocaine regional anaesthesian in patients undergoing bone marrow biopsy | |||||||||||||
Medical condition: Patients suffering from different forms of leukemia | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010696-24 | Sponsor Protocol Number: 87906883 | Start Date*: 2009-04-24 | ||||||||||||||||
Sponsor Name:Helsinki University Central Hospital | ||||||||||||||||||
Full Title: Artikaiinin ja fentanyyli-artikaiinin vertailu päiväkirurgisten alaraajaleikkauspotilaiden spinaalipuudutteena | ||||||||||||||||||
Medical condition: Kyseessä (vähintään 18-vuotiaita) aikuispotilaita, joilla on päiväkirurgisesti hoidettava alaraajan ortopedinen sairaus | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004741-16 | Sponsor Protocol Number: TRAMAPIMD-001 | Start Date*: 2014-07-25 | ||||||||||||||||||||||||||
Sponsor Name:Ana de Pedro Muñoz | ||||||||||||||||||||||||||||
Full Title: Effect of preoperatory administration of submucous tramadol on the success rate of inferior alveolar nerve block on mandibular molars with irreversible pulpitis | ||||||||||||||||||||||||||||
Medical condition: Anesthetic failure of the inferior alveolar nerve block in mandibular molars with irreversible pulpitis | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003031-70 | Sponsor Protocol Number: N-ART-06-112 | Start Date*: 2006-11-29 | |||||||||||
Sponsor Name:LABORATORIOS NORMON S.A. | |||||||||||||
Full Title: Evaluación de la profundidad anestésica de la lidocaína 1:100.000 frente a la articaína 1:100.000, en la cirugía del tercer molar inferior. Estudio comparativo | |||||||||||||
Medical condition: Estudio paralelo de eficacia anestésica con las combinaciones de articaína y lidocaína con epinefrina en la extracción del tercer molar inferior en pacientes con tercer molar inferior retenido. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
