- Trials with a EudraCT protocol (27)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
27 result(s) found for: Dental Anesthesia.
Displaying page 1 of 2.
EudraCT Number: 2016-001567-37 | Sponsor Protocol Number: KUKIDEX-2 | Start Date*: 2016-11-24 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Efficacy of single dose intranasal dexmedetomidine for conscious sedation in dental practice in dentophobic uncooperative patients with intellectual disability. | ||
Medical condition: dentophobia intellectual disability | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-019712-20 | Sponsor Protocol Number: DCSP1 | Start Date*: Information not available in EudraCT |
Sponsor Name:University of Oslo, Institute of Clinical Dentistry | ||
Full Title: D-CYCLOSERINE ENHANCEMENT OF EXPOSURE TREATMENT OF DENTALLY FEARFUL AND AVOIDANT CHILDREN. A PILOT STUDY | ||
Medical condition: Avoidance of dental care because of dental anxiety often result in reduced dental health and need for sedation or treatment in general anesthesia. Treatment of dental anxiety is time consuming and ... | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NO (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-001797-27 | Sponsor Protocol Number: 2005/142 | Start Date*: 2005-08-01 |
Sponsor Name:University Hospital Ghent | ||
Full Title: Accuracy of the Kataria model for propofol anesthesia in children | ||
Medical condition: Dental and eye treatment under general anesthesia | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002243-17 | Sponsor Protocol Number: DEXCOM | Start Date*: 2014-10-24 | |||||||||||
Sponsor Name:Clínica Universidad de Navarra/Universidad de Navarra | |||||||||||||
Full Title: Conscious sedation for procedures in Dental and Minor Maxillofacial Surgery Unit: optimization of the dexmedetomidine dose (Dexdor®). | |||||||||||||
Medical condition: Sedation for procedures in Dental and Minor Maxillofacial Surgery Unit | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
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 | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003430-16 | Sponsor Protocol Number: OC004PDS | Start Date*: 2012-11-15 | |||||||||||
Sponsor Name:Clinical Reasearch Centre, Hvidovre University Hospital | |||||||||||||
Full Title: Effect of local anesthesia in patients with marginal periodontitis undergoing subgingival scaling | |||||||||||||
Medical condition: Pain and discomfort during dental treatment in patients with periodontitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004481-16 | Sponsor Protocol Number: VRA105345 | Start Date*: 2005-12-19 |
Sponsor Name:GlaxoSmithKline Research and Development | ||
Full Title: A multi-centre, randomised, single blind, placebo controlled, parallel group study to examine the effect of single doses of SB-705498, a TRPV1 receptor antagonist, on pain following third molar too... | ||
Medical condition: Dental pain | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-004655-23 | Sponsor Protocol Number: CR4056-2-03 | Start Date*: 2018-09-24 | |||||||||||
Sponsor Name:Rottapharm Biotech s.r.l. | |||||||||||||
Full Title: A randomized, double-blind, active- and placebo-controlled, parallel group, single dose, multicentre study to assess the analgesic effect of CR4056 in postoperative dental pain | |||||||||||||
Medical condition: Postoperative dental pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005278-12 | Sponsor Protocol Number: BAY1019036/15082 | Start Date*: 2015-02-09 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized, Parallel, Placebo-Controlled Trial Assessing the Analgesic Efficacy of a Single, Oral Dose of a Fast Release Aspirin 650 mg in Postsurgical Dental Pain | |||||||||||||
Medical condition: postsurgical (extraction) dental pain | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005271-81 | Sponsor Protocol Number: BAY1019036/15120 | Start Date*: 2015-02-09 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized, Parallel, Placebo-Controlled Trial Assessing the Analgesic Efficacy of a Single, Oral Dose of a Fast Release Aspirin 1000 mg in Postsurgical Dental Pain | |||||||||||||
Medical condition: postsurgical dental pain | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001412-30 | Sponsor Protocol Number: FMLD-FEBETRADI-PILOT-43_FIII | Start Date*: 2018-07-13 | |||||||||||
Sponsor Name:Laboratorios Farmalíder S.A. | |||||||||||||
Full Title: Double blind, randomized, pilot clinical trial controlled with placebo to evaluate the comparative efficacy of ibuprofen combined with different doses of tramadol and tramadol 100 mg by intravenous... | |||||||||||||
Medical condition: Moderate-Intense pain in Dental Surgery | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004637-33 | Sponsor Protocol Number: FMLD-IOTRA-20_FIIIA | Start Date*: 2014-06-11 |
Sponsor Name:Laboratorios Farmalider S.A. | ||
Full Title: Clinical trial phase III, multicenter, randomised, double-blind, double-dummy, parallel treatment design, active-controlled and placebo, to evaluate the analgesic efficacy and safety of ibuprofen a... | ||
Medical condition: Moderate to severe pain following dental surgery. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-000254-13 | Sponsor Protocol Number: RD/613/07 | Start Date*: 2008-10-14 | ||||||||||||||||
Sponsor Name:Gwent Healthcare NHS Trust | ||||||||||||||||||
Full Title: A double blind randomised placebo controlled study assessing the effect of intra-operative local anaesthetic administration on postoperative pain in adolescent children undergoing oral surgery unde... | ||||||||||||||||||
Medical condition: Postoperative pain following oral surgery in 12 to 16 year olds | ||||||||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005530-15 | Sponsor Protocol Number: FMLD-IOTRA2-47_FIII | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Farmalíder S.A. | |||||||||||||
Full Title: Randomized, double blind, placebo-controlled, active treatment clinical trial to assess the analgesic efficacy and the safety of an oral ibuprofen (arginine)-tramadol HCI combination administered t... | |||||||||||||
Medical condition: Moderate-severe somatic pain | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Restarted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005305-31 | Sponsor Protocol Number: 2013v01 | Start Date*: 2014-03-24 |
Sponsor Name:Folktandvården Östergötland | ||
Full Title: Ice as topical anaesthesia before injection in the oral mucosa –a randomized unblinded cross-over study in adolescents. Comparison between ice and lidokain gel 5%. | ||
Medical condition: The patients should be < 20 years and reffered by an orthodontist with two contra lateral premolars in the upper jaw that has to be extracted. They should not have any diseases or medications that,... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002778-21 | Sponsor Protocol Number: ESTEVE-SACO4-201 | Start Date*: 2012-01-12 | |||||||||||
Sponsor Name:Laboratorios del Dr. Esteve, S.A | |||||||||||||
Full Title: A randomized, double-blind, controlled with active treatment (tramadol 100 mg) and placebo, parallel groups, Phase II clinical trial to establish the effective dose between 4 strengths of E-58425 f... | |||||||||||||
Medical condition: Adult patients with moderate to severe dental pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000727-12 | Sponsor Protocol Number: RC31/20/0443 | Start Date*: 2021-06-28 |
Sponsor Name:University Hospital of Toulouse | ||
Full Title: Quality Assessment of Tracheal intubation without neuromuscular blocking drugs (Propofol+ Remifentanil) in obese patients: Pilot Study | ||
Medical condition: induction phase of the general anesthesia in obese patients | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-005270-11 | Sponsor Protocol Number: BAY1019036/15529 | Start Date*: 2015-02-09 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: Comparative Onset of Action of a Fast Release Aspirin Tablet in a Dental Impaction Pain Model | |||||||||||||
Medical condition: pain following extraction of impacted third molars | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004671-39 | Sponsor Protocol Number: 2019/318 | Start Date*: Information not available in EudraCT |
Sponsor Name:Universitair Ziekenhuis Brussel (UZ Brussel) | ||
Full Title: The effect of handheld-multimedia versus midazolam premedication on the level of perioperative anxiety in pediatric day-care. A randomized controlled trial. | ||
Medical condition: Perioperative anxiety in children scheduled for an elective circumcision, dental care or tonsillectomy/adenoidectomy in day-care | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: BE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-005575-14 | Sponsor Protocol Number: R-01270-A015 | Start Date*: 2006-08-08 |
Sponsor Name:Baxter R&D Europe S.C.R.L | ||
Full Title: A randomized, double-blind, placebo-controlled, single-dose, parallel-group comparison of the analgesic efficacy, safety and local tolerability of intravenous paracetamol 1% solution Bioren (test),... | ||
Medical condition: Post-surgical dental pain after removal of one or more impacted 3rd mandibular molar(s), associated with moderate to severe pain. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
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