- Trials with a EudraCT protocol (11)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
11 result(s) found for: Maxillofacial surgery.
Displaying page 1 of 1.
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: 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: 2014-004975-22 | Sponsor Protocol Number: ORN-2014-16 | Start Date*: 2015-09-03 |
Sponsor Name:Oral and Maxillofacial Surgery Department of Vall d'Hebron Hospital | ||
Full Title: Advances in the management of mandibular osteoradionecrosis: Pentoxyfilline and Tocopherol as medical treatment. | ||
Medical condition: Assess whether there is a clinically significant reduction in intraoral bone exposure (measured in mm) in the experimental group after the start of treatment with pentoxifylline and tocopherol (PEN... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-002645-54 | Sponsor Protocol Number: Dexmatod | Start Date*: 2015-12-23 |
Sponsor Name:Universitair Ziekenhuis Brussel | ||
Full Title: Comparison of efficacy between dexmedetomidine (DEX) and nicardipine (NIC) in adult facial surgery | ||
Medical condition: - maxillofacial surgery - pain relief requirement - surgical vision - hemodynamic stability - propofol remifentanil use | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-005473-52 | Sponsor Protocol Number: 40964 | Start Date*: 2014-04-24 | |||||||||||
Sponsor Name:Hospital of South West Jutland | |||||||||||||
Full Title: Prevention of bleeding and edema in bi-maxillary orthognathic surgery; the effectiveness of tranexamic acid on intraoperative bleeding in orthognathic surgery | |||||||||||||
Medical condition: Surgical bleeding during bi-maxillary orthognathic surgery | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
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: 2006-001367-36 | Sponsor Protocol Number: DoxP-01/2006 | Start Date*: 2006-12-05 | |||||||||||
Sponsor Name:Prof. Dr. Peter Eickholz | |||||||||||||
Full Title: Benefit of adjunctive systemic postsurgical doxycycline in regenerative periodontal surgery | |||||||||||||
Medical condition: Periodontitis is an opportunistic infectious disease that destroys the periodontal attachment and bone. Bacterial plaque (biofilm) on the teeth adjacent to the gingiva is the necessary cause gingiv... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001434-16 | Sponsor Protocol Number: 3D_CHB/collacone | Start Date*: 2016-03-30 | |||||||||||
Sponsor Name:Universitätsmedizin Greifswald, KöR | |||||||||||||
Full Title: A method for measuring volume changes of the alveolar ridge during dental implantation using 3D scanning | |||||||||||||
Medical condition: alveolar ridge atrophy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004564-26 | Sponsor Protocol Number: BAS20 | Start Date*: 2021-09-20 | |||||||||||
Sponsor Name:Karolinska Institute | |||||||||||||
Full Title: Role of antibiotics in conjunction with oral bone augmentation procedures (BAS20) | |||||||||||||
Medical condition: Patients requiring bone augmentation procedure prior to, or in conjunction to installation of dental implants. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004587-11 | Sponsor Protocol Number: KUKIDEX-1 | Start Date*: 2016-01-08 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Safety, tolerability and sedative properties of single dose intranasal dexmedetomidine premedication in elderly subjects. | ||
Medical condition: Anxiety, preoperative | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-016668-35 | Sponsor Protocol Number: HBO-CPH1 | Start Date*: 2009-12-22 | |||||||||||
Sponsor Name:Copenhagen University Hospital | |||||||||||||
Full Title: Hyperbaric Oxygen - a new treatment modality in patients with salivary gland radiation injury | |||||||||||||
Medical condition: Late radiation tissue injury to salivary glands | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
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