- Trials with a EudraCT protocol (55)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
55 result(s) found for: Dentistry.
Displaying page 1 of 3.
| EudraCT Number: 2012-003139-50 | Sponsor Protocol Number: Maxillo1 | Start Date*: Information not available in EudraCT |
| Sponsor Name:University of Bergen, Faculty of medicin and dentistry, Dep. of Clinical Dentistry | ||
| Full Title: International, multicenter phase II uncontrolled prospective clinical trial: Jaw bone reconstruction using a combination of biomaterial and autologous mesenchymal stem cells prior to dental impla... | ||
| Medical condition: Men and women aged 18 years or more requiring jaw bone reconstruction prior to dental implant placement based on clinical and radiological examinations (CBCT Cone beam CT imaging). Areas suitable ... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (Completed) | ||
| Trial results: (No results available) | ||
| 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: 2022-003117-11 | Sponsor Protocol Number: BCD101 | Start Date*: 2023-10-24 | |||||||||||
| Sponsor Name:Dentlabe s.r.o. | |||||||||||||
| Full Title: Study assessing if oxytocin can be used as premedication for anxious patients in dentistry. | |||||||||||||
| Medical condition: Premedication in dentistry | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-005758-39 | Sponsor Protocol Number: 9812/A | Start Date*: 2006-08-16 |
| Sponsor Name:Greater Glasgow Health Board | ||
| Full Title: Effect site controlled, reaction time safeguarded, patient maintained sedation with Propofol A) in oral surgery patients B) in general dentistry patients C) in colonoscopy patients | ||
| Medical condition: No specific medical condition. IMP will be used to provide conscious sedation for patients undergoing potentially unpleasant procedures including dentistry and colonoscopy. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-000213-33 | Sponsor Protocol Number: 14012020 | Start Date*: 2020-04-21 | |||||||||||
| Sponsor Name:Department of Dentistry and Oral Health | |||||||||||||
| Full Title: Fluoride in saliva during and after use of high-fluoride toothpaste | |||||||||||||
| Medical condition: Not applicable. A physiological phenomena is explored. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-005074-19 | Sponsor Protocol Number: BRIDION_ERASME | Start Date*: 2018-04-06 |
| Sponsor Name:Erasme Hospital | ||
| Full Title: Minimal optimal dose of Sugammadex during ambulatory surgery in dentistry | ||
| Medical condition: women and men> 18 years of age Elective Surgery BMI <30, patients who gave consent to free and informed participation in writing to benefit from tooth extraction | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-000714-15 | Sponsor Protocol Number: CCBNB406201942446 | Start Date*: Information not available in EudraCT |
| Sponsor Name:ULB ERASME | ||
| Full Title: Phentolamines and their role in everyday dentistry | ||
| Medical condition: Patients with dental decay, root canal treatment or tooth to be extracted will be studied | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: BE (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-000501-26 | Sponsor Protocol Number: NanofatTMJ | Start Date*: 2022-08-24 |
| Sponsor Name:University of Tartu Institute of Dentistry | ||
| Full Title: Effect of non-enriched grafting of emulsified adipose tissue in patients with temporomandibular joint osteoarthritis. | ||
| Medical condition: Temporomandibular osteoarthritis. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: EE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-001885-40 | Sponsor Protocol Number: Syst-AB+Sinus | Start Date*: 2022-02-24 |
| Sponsor Name:Universidad Complutense de Madrid | ||
| Full Title: The effect of systemic antibiotics on post-surgical complications and paitent-centered outomes in patients undergoing implant surgery with the guided bone regeneration and simultaneous sinus floor ... | ||
| Medical condition: The medical condition that the patients have in this trial is edentulism in a posterior maxillary quadrant of the mouth with a sinus pneumatisation/ decreased crestal bone heigh defect requiring a... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| 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: 2021-005374-26 | Sponsor Protocol Number: ECAELEV21 | Start Date*: 2022-08-18 |
| Sponsor Name:OMEQUI coordinator | ||
| Full Title: Efficacy of platelet- and leukocyte-rich fibrin (L-PRF) in reducing healing time in sinus lift combined with deproteinized bovine mineralized bone (DBBM): randomized clinical trial. | ||
| Medical condition: If the application of L-PRF with respect to the use of DBBM shows that there are differences in the percentage of new bone between the LPRF group and the control group at 4 and 6 months | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-000156-33 | Sponsor Protocol Number: RBHP_2012_DALLEL | Start Date*: 2012-06-12 |
| Sponsor Name:CHU de Clermont-Ferrand | ||
| Full Title: | ||
| Medical condition: | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FR (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-001227-39 | Sponsor Protocol Number: 779322 | Start Date*: 2019-12-11 | |||||||||||
| Sponsor Name:University of Bergen, Faculty of Medicin, Department of Clinical Dentistry | |||||||||||||
| Full Title: A randomized controlled clinical trial to assess the efficacy of a combination of autologous mesenchymal stem cells and biomaterial in jaw bone regeneration prior to dental implant placement in com... | |||||||||||||
| Medical condition: Patients in need of dental implant(s) in the upper and lower jaws with presence of bone defects with loss in vertical height and < than 4 mm in lateral width | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) NO (Completed) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-001068-39 | Sponsor Protocol Number: ECPAF11/16 | Start Date*: 2018-07-24 |
| Sponsor Name:OMEQUI | ||
| Full Title: Changes in the bone morphology of the post-extraction socket, preserved with platelet-rich fibrin and leukocytes (L-PRF) versus Conventional treatment | ||
| Medical condition: Regenerative potential of L-PRF | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-005253-30 | Sponsor Protocol Number: 9876543123xz | Start Date*: 2006-12-22 |
| Sponsor Name:Queen Mary's School of Medicine & Dentistry, University of London | ||
| Full Title: Study of the effects of different targets for perfusion pressure on tissue perfusion and oxygenation in patients suffering from septic shock | ||
| Medical condition: Septic shock | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| 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: 2017-002532-16 | Sponsor Protocol Number: 02 | Start Date*: 2017-12-05 |
| Sponsor Name:Cliniques Universitaires Saint-Luc | ||
| Full Title: Adjunctive systemic antimicrobial therapy in the surgical treatment of peri-implantitis. A prospective randomized clinical study | ||
| Medical condition: To treat patients with chronic infection of dental implants. One group with antibiotics and one group without. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-004986-28 | Sponsor Protocol Number: AMOXI | Start Date*: 2019-03-25 | ||||||||||||||||
| Sponsor Name:Medizinische Universität Graz, Klin. Abteilung für Orale Chirurgie und Kieferorthopädie | ||||||||||||||||||
| Full Title: Effect of systemic antibiotic therapy on postoperative complications in patients undergoing wisdom teeth removal surgery. A double-blind, randomised, placebo-controlled Trial | ||||||||||||||||||
| Medical condition: Surgical extraction of third molars | ||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: AT (Completed) | ||||||||||||||||||
| 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 (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-022334-92 | Sponsor Protocol Number: qmul250510 | Start Date*: 2011-01-07 |
| Sponsor Name:Barts and the London School of Medicine and Dentistry, Queen Mary University of London | ||
| Full Title: Effects of a combination of varenicline and transdermal nicotine patch on post-quitting urges to smoke | ||
| Medical condition: Tobacco dependence (smoking cessation) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
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