- Trials with a EudraCT protocol (35)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (17)
35 result(s) found for: Third Molar.
Displaying page 1 of 2.
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: 2019-000736-25 | Sponsor Protocol Number: IB3M.2019 | Start Date*: 2019-09-05 |
Sponsor Name:Universidad Complutense de Madrid | ||
Full Title: Efficacy of Non-Steroidal Anti-Inflammatory (Ibuprofen) Chronotherapy in Healing After Mandibular Third Molar Surgical Extraction – A Randomized Clinical Trial | ||
Medical condition: The clinical trial will try to understand if the elimination of the ibuprofen dosage in resting phase after surgical third molar extraction not jeopardize the postoperative period . | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000193-77 | Sponsor Protocol Number: 05/Q1405/78 | Start Date*: 2007-03-20 |
Sponsor Name:The University of Manchester | ||
Full Title: Protective analgesia using bupivacaine and conventional release ibuprofen versus bupivacaine and sustained release ibuprofen for postoperative pain relief in patients undergoing third molar surgery... | ||
Medical condition: Pain following surgical removal of impacted lower wisdom tooth/ teeth. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004682-24 | Sponsor Protocol Number: DC0071BB405 | Start Date*: 2015-04-27 | |||||||||||
Sponsor Name:Institut de Recherche Pierre Fabre - Centre de R&D Pierre Fabre | |||||||||||||
Full Title: Efficacy of DC071 mouthwash (0,2 % chlorhexidine digluconate) in peri-surgical care for preventing alveolar osteitis after third molar extraction. Prospective, multicenter, randomised, double-blin... | |||||||||||||
Medical condition: Prevention of alveolar osteitis after third molar extraction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) LV (Completed) LT (Completed) FR (Completed) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004083-62 | Sponsor Protocol Number: steroid3848 | Start Date*: 2019-09-06 |
Sponsor Name:Semmelweis University, Oro-Maxillofacial Surgery and Stomatology | ||
Full Title: Effect of preoperative intramasseteric methylprednisolone injection on the post-operative sequelae of lower third molar surgery: a placebo controlled, randomized, double-blinded study | ||
Medical condition: post-operative swelling, trismus, pain | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000622-35 | Sponsor Protocol Number: 56872 | Start Date*: 2017-10-23 | |||||||||||
Sponsor Name:Aalborg University Hospital | |||||||||||||
Full Title: Different dosis of corticosteroids in mandibular third molar surgery. A randomized, blinded clinical trial assessing pain, trismus, edema, and quality of life outcome measurements. | |||||||||||||
Medical condition: The purpose is to investigate the postoperative morbidity after removal of mandibular third molar with different doses of methylprednisolone. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000901-31 | Sponsor Protocol Number: 18122006 | Start Date*: 2007-05-15 |
Sponsor Name:Universitair Ziekenhuis Antwerpen | ||
Full Title: A DOUBLE-BLIND? PLACEBO-CONTROLLED PARALLEL ARM TRIAL TO STUDY THE EFFICACY OF A SINGLE ORAL DOSE OF THE NUCLEOSIDE TRANSPORT INHIBITOR DIPYRIDAMOLE FOR PAIN RELIEF IN PATIENTS AFTER THIRD MOLAR SU... | ||
Medical condition: Pain after third molar surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-003258-21 | Sponsor Protocol Number: PDC-01-0205 | Start Date*: 2022-05-19 | |||||||||||
Sponsor Name:Cessatech A/S | |||||||||||||
Full Title: Analgesic Efficacy and Pharmacokinetic-pharmacodynamic Relationship of Intranasally Administered Sufentanil, Ketamine, and CT001 after Impacted Mandibular Third Molar Extraction | |||||||||||||
Medical condition: Healthy male or female participants scheduled for surgical removal of an impacted mandibular third molar, where bone removal is judged to be needed. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002784-27 | Sponsor Protocol Number: Stei-Azurcomp-0107 | Start Date*: 2008-01-18 | |||||||||||
Sponsor Name:Steiner & Co. Deutsche Arzneimittelgesellschaft mbH & Co. KG | |||||||||||||
Full Title: Randomised, double-blind, prospective multi-centre study to compare the analgesic efficacy and safety of a paracetamol/codeine/caffeine fixed-dose combination (Azur® compositum) with paracetamol/co... | |||||||||||||
Medical condition: Post-operative pain after a dental surgical procedure (third molar surgery). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003976-20 | Sponsor Protocol Number: GRC6211-201 | Start Date*: 2007-09-12 | |||||||||||
Sponsor Name:GLENMARK PHARMACEUTICALS SA | |||||||||||||
Full Title: A randomised, double blind, placebo and active controlled, parallel group study to evaluate the analgesic effect of a single dose of GRC 6211, a TRPV1 receptor antagonist on pain following third... | |||||||||||||
Medical condition: treatment of pain following third molar extraction | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000902-31 | Sponsor Protocol Number: ECACOR19 | Start Date*: 2019-09-05 |
Sponsor Name:OMEQUI | ||
Full Title: Healing efficacy after impacted mandibular third molar surgery with the use of autologous platelet-rich fibrin: a randomized controlled clinical study | ||
Medical condition: If the addition of L-PRF reduces postoperative pain and inflammation, as well as complications, after extraction of lower third molars | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000200-14 | Sponsor Protocol Number: | Start Date*: 2005-07-08 |
Sponsor Name:North Bristol NHS Trust | ||
Full Title: A randomised, double-blinded comparison of the effectiveness of intravenously administered Ketoralac versus Dexamethasone in the treatment of pain following surgical removal of third molar teeth un... | ||
Medical condition: Pain experienced after the surgical removal of impacted third molars. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-005478-66 | Sponsor Protocol Number: PDY5808 | Start Date*: 2006-02-09 | |||||||||||
Sponsor Name:Sanofi-Synthelabo Recherche | |||||||||||||
Full Title: Effect of a single oral 120 µg dose of SSR150106XB compared to placebo on the assessment of post dental surgical pain after extraction of an impacted or partially impacted third molar in 90 male an... | |||||||||||||
Medical condition: Men and women who are to undergo elective surgery for extraction of at least one lower impacted or partially impacted third molar | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004790-10 | Sponsor Protocol Number: A2720382 | Start Date*: 2007-06-06 | |||||||||||
Sponsor Name:GlaxoSmithKline Consumer Healthcare | |||||||||||||
Full Title: A Proof-of-Principle Analgesic Adjuvant Pilot Study in Post-Operative Dental Pain | |||||||||||||
Medical condition: Analgesia induced by dental extraction | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002691-18 | Sponsor Protocol Number: CBA106809 | Start Date*: 2006-10-03 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development | |||||||||||||
Full Title: A multi-centre, randomised, single-blind, placebo-controlled, parallel group study to investigate the efficacy of single pre-emptive doses of GW842166X, a non-cannabinoid CB2 receptor agonist, on p... | |||||||||||||
Medical condition: Inflammatory Pain | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) IT (Completed) DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000535-86 | Sponsor Protocol Number: HAP.2011-002 | Start Date*: 2011-03-29 | |||||||||||
Sponsor Name:CHU AMBROISE PARE | |||||||||||||
Full Title: A PHASE IIb STUDY TO EVALUATE THE EFFICACY AND SAFETY OF ROPIVACAINE COMPARED TO ADRENALINE-LIDOCAINE TO REDUCE PAIN IN PATIENT UNDERGOING SURGERY FOR THIRD MOLAR TEETH EXTRACTION. | |||||||||||||
Medical condition: third molar theeth included needing surgical extraction | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2015-004152-22 | Sponsor Protocol Number: DEX-TRA-06 | Start Date*: 2016-03-01 | |||||||||||
Sponsor Name:MENARINI RICERCHE S.p.A. | |||||||||||||
Full Title: Analgesic efficacy of oral dexketoprofen trometamol/tramadol hydrochloride versus tramadol hydrochloride/paracetamol: a randomised, double-blind, placebo and active-controlled, parallel group study... | |||||||||||||
Medical condition: moderate to severe acute pain after removal of impacted lower third molar | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) HU (Completed) ES (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000592-24 | Sponsor Protocol Number: MR308-3501 | Start Date*: 2017-03-15 | |||||||||||
Sponsor Name:Mundipharma Research GmbH & Co. KG | |||||||||||||
Full Title: A Randomized, Double-Blind, Multicenter, Placebo- and active Comparator-Controlled Study to evaluate Efficacy and Safety of MR308 in the Treatment of Acute Pain After Third Molar Tooth Extraction (... | |||||||||||||
Medical condition: Acute pain after third molar tooth extraction; dental procedure must have involved extraction of at least two impacted third molars requireing bone removal. If only two impacted third molars are ex... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003323-11 | Sponsor Protocol Number: ITIBU001 | Start Date*: 2014-10-01 | ||||||||||||||||
Sponsor Name:"Sapienza" University of Rome | ||||||||||||||||||
Full Title: RANDOMIZED CLINICAL TRIAL, PLACEBO-CONTROLLED, SPLIT-MOUTH, A DOUBLE-BLIND, FOR THE EVALUATION OF THE EFFECTIVENESS OF PREemptive ANALGESIA BY ADMINISTRATION OF IBUPROFEN 400MG, FOR THE CONTROL ... | ||||||||||||||||||
Medical condition: POST-OPERATIVE ACUTE PAIN (DAPO) | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
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