- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
8 result(s) found for: Vaginal trauma.
Displaying page 1 of 1.
| EudraCT Number: 2015-003412-20 | Sponsor Protocol Number: DV-MV-MO | Start Date*: 2016-08-01 |
| Sponsor Name:Basque Health System | ||
| Full Title: Efficacy and safety of hourly titrated misoprostol versus vaginal dinoprostone and misoprostol for cervical ripening and labor induction: randomized clinical trial. | ||
| Medical condition: labor induction | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-000356-33 | Sponsor Protocol Number: oxy123 | Start Date*: 2013-03-27 | |||||||||||
| Sponsor Name:Västra Götaland | |||||||||||||
| Full Title: Delay in labour due to ineffective uterine contractions is still a major problem in modern obstetric care. It is one of the main reasons for the increased rate of operative deliveries, particularly... | |||||||||||||
| Medical condition: Labor dystocia (LD) also referred to as prolonged labour is a commonly identified problem in modern delivery care with three described possible causes: inefficient uterine action, occiputposterior ... | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: SE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-017418-56 | Sponsor Protocol Number: BSH-10 | Start Date*: 2010-04-07 |
| Sponsor Name:Birken GmbH | ||
| Full Title: Open, Prospective, Controlled, Randomised, Multicenter Phase II Clinical Trial to Compare Intra-individually the Efficacy and Tolerance of Oleogel-S10 versus Moist Wound Healing Dressing alone in A... | ||
| Medical condition: Es handelt sich um eine offene, prospektive, kontrollierte, randomisierte, multizentrische Studie der Phase II, die eine intra-individuelle Wirksamkeit und Verträglichkeit des Oleogel-S10 mit einer... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-000489-40 | Sponsor Protocol Number: IZD174-002 | Start Date*: 2020-09-22 | |||||||||||
| Sponsor Name:Inflazome (Australia) Pty Ltd. | |||||||||||||
| Full Title: A Multi-Centre, Randomised, Open-Label, Phase IIb Study to Evaluate the Safety, Tolerability and Efficacy of IZD174 in Patients with Cryopyrin Associated Periodic Syndromes | |||||||||||||
| Medical condition: Cryopyrin-associated periodic syndrome (CAPS) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-002880-82 | Sponsor Protocol Number: GUARD | Start Date*: 2020-05-05 | |||||||||||
| Sponsor Name:King's College London [...] | |||||||||||||
| Full Title: Randomised controlled trial of Gestational treatment with Ursodeoxycholic Acid compared to Metformin to Reduce effects of Diabetes mellitus | |||||||||||||
| Medical condition: Gestational Diabetes Mellitus | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-000245-33 | Sponsor Protocol Number: VN21 | Start Date*: 2022-05-31 | |||||||||||
| Sponsor Name:Medical University of Lublin | |||||||||||||
| Full Title: To evaluate the effect of low-dose naltrexone (LDN) on pain perception and quality of life in women | |||||||||||||
| Medical condition: Vulvodynia | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: PL (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-001727-39 | Sponsor Protocol Number: POP03 | Start Date*: 2018-10-16 | ||||||||||||||||
| Sponsor Name:Polpharma S.A. | ||||||||||||||||||
| Full Title: A PHASE III, MULTICENTRE, RANDOMISED, INVESTIGATOR-MASKED, CROSSOVER, COMPARATIVE, NON-INFERIORITY TRIAL EVALUATING THE EFFICACY AND TOLERABILITY OF GENERIC LATANOPROST 0.05 MG/ML EYE DROPS SOLUTIO... | ||||||||||||||||||
| Medical condition: Ocular hypertension and open angle glaucoma | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: HU (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2004-001200-12 | Sponsor Protocol Number: A5951002 | Start Date*: 2007-08-27 | |||||||||||
| Sponsor Name:Pfizer Global Research and Development | |||||||||||||
| Full Title: Linezolid In The Treatment Of Complicated Skin And Soft Tissue Infections Proven To Be Due To Methicillin-Resistant Staphylococcus Aureus | |||||||||||||
| Medical condition: Complicated skin and soft tissue infections | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Completed) GB (Completed) ES (Completed) BE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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Query did not match any studies.