- Trials with a EudraCT protocol (4)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
4 result(s) found for: Vertical muscle.
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| EudraCT Number: 2021-000240-22 | Sponsor Protocol Number: M21-310 | Start Date*: 2021-11-24 |
| Sponsor Name:AbbVie | ||
| Full Title: A Phase 3 Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety and Efficacy of BOTOX® (Botulinum Toxin Type A) Purified Neurotoxin Complex for the Treatment of Pla... | ||
| Medical condition: Moderate and severe platysma prominence | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2022-000788-30 | Sponsor Protocol Number: 1.2022 | Start Date*: 2023-04-13 |
| Sponsor Name:Uzdrowisko Kamień Pomorski S.A. | ||
| Full Title: Evaluation of the effectiveness of Methocarbamol in the treatment of spasticity in people with spinal cord injury. | ||
| Medical condition: | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: PL (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-004377-41 | Sponsor Protocol Number: TFP_1-1 | Start Date*: 2016-12-19 | |||||||||||
| Sponsor Name:Dep. Anaesthesia and Intensive Care, Aarhus University Hospital | |||||||||||||
| Full Title: Regional anaesthesia of the cutaneus nerves of the hip - A randomized controlled trial of the transversalis fascia plane block | |||||||||||||
| Medical condition: Postoperative pain after hip surgery | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-003790-41 | Sponsor Protocol Number: JAN12006-01 | Start Date*: 2015-05-11 |
| Sponsor Name:Spherium Biomed | ||
| Full Title: Randomised, double-blinded, placebo and active comparator controlled exploratory clinical trial to assess the efficacy and safety of a triple combination of Ibuprofen, magnesium and ascorbic acid ... | ||
| Medical condition: Temporomandibular joint dysfunction syndrome. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
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Query did not match any studies.