- Trials with a EudraCT protocol (10)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
10 result(s) found for: Trismus.
Displaying page 1 of 1.
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: 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: 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: 2007-006252-19 | Sponsor Protocol Number: 1.0. | Start Date*: 2008-07-24 |
Sponsor Name:Univ.-Prof. DDr. Norbert Jakse, Universitätszahnklinik Graz, Dep. f. Orale Chirurgie u. Röntgenologi | ||
Full Title: Einfluss von peroraler Methylprednisolon-Gabe auf die postoperative Morbidität nach operativer Weisheitszahnenfernung im Unterkiefer. (Influence of peroral Methylprednisolone administration on the... | ||
Medical condition: To be investigated is the anti-inflammatory and anti-oedematous effect of methylprednisolone on the postoperative sequelae after surgical removal of lower third molars. 16 healthy patients will und... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001153-27 | Sponsor Protocol Number: PenVe | Start Date*: 2019-02-22 | |||||||||||||||||||||
Sponsor Name:Guy's and St Thomas' NHS Foundation Trust | |||||||||||||||||||||||
Full Title: A feasibility study of a prospective randomised controlled trial comparing the use of open label pentoxifylline and tocopherol versus current standard of care for the prevention of fibrosis related... | |||||||||||||||||||||||
Medical condition: Osteoradionecrosis, trismus and dysphagia | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
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: 2022-002669-13 | Sponsor Protocol Number: 87RI21_0052 | Start Date*: 2022-11-25 | |||||||||||
Sponsor Name:Limoges University Hospital | |||||||||||||
Full Title: The PENTO protocol in Medication-related osteonecrosis of the jaw (MRONJ): a single-center phase IIa trial | |||||||||||||
Medical condition: Medication-related osteonecrosis of the jaw (MRONJ) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007842-36 | Sponsor Protocol Number: DAHANCA-21 | Start Date*: 2008-05-05 | |||||||||||
Sponsor Name:Lone Elisabeth Forner | |||||||||||||
Full Title: Hyperbaric oxygen treatment of mandibular osteoradionecrosis. A randomized clinical trial. | |||||||||||||
Medical condition: Mandibular osteoradionecrosis occuring from radiation treatment of cancer. No healthy volunteers | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002996-32 | Sponsor Protocol Number: 12UK/DCsc04 | Start Date*: 2012-11-12 | |||||||||||
Sponsor Name:IBSA Institut Biochimique S.A. | |||||||||||||
Full Title: Preliminary evaluation of the efficacy and local tolerability of Injectable Diclofenac at 5, 12.5, 25 and 50 mg/mL, administered locally prior to surgery for the prevention of post-operative pain a... | |||||||||||||
Medical condition: post-surgical pain after lower third molar removal. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2016-001916-39 | Sponsor Protocol Number: AB0001 | Start Date*: 2016-09-09 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA PISANA | ||||||||||||||||||
Full Title: A phase IV, single-blind, randomized, controlled, single-center study evaluating the efficacy of amoxicillin+clavulanic acid Vs no treatment in preventing complications after tooth extraction and t... | ||||||||||||||||||
Medical condition: teeth needing extraction due to infections | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
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