- Trials with a EudraCT protocol (7)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
7 result(s) found for: Impacted wisdom teeth.
Displaying page 1 of 1.
| 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: 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: 2019-000902-31 | 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: 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) | ||||||||||||||||||
| EudraCT Number: 2012-005807-41 | Sponsor Protocol Number: PRE-EMPTIVE | Start Date*: 2013-04-28 | ||||||||||||||||
| 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 PRE-emptive ANALGESIA BY ADMINISTRATION OF PARACETAMOL 500MG + codeine 30mg, ... | ||||||||||||||||||
| 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) | ||||||||||||||||||
| EudraCT Number: 2020-002220-37 | Sponsor Protocol Number: UP-CLI-2020-001 | Start Date*: 2021-02-24 |
| Sponsor Name:UNITHER Pharmaceuticals | ||
| Full Title: Comparison of the analgesic effect of a new paracetamol formulation (paracetamol UNIFLASH) for buccal use and two different doses of an oral paracetamol form controlled versus placebo in patients s... | ||
| Medical condition: Symptomatic short-term treatment of moderate pain | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) IT (Completed) | ||
| Trial results: (No results available) | ||
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