- Trials with a EudraCT protocol (5)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
5 result(s) found for: Bandages.
Displaying page 1 of 1.
| EudraCT Number: 2005-001551-38 | Sponsor Protocol Number: ghnhsft | Start Date*: 2005-09-29 |
| Sponsor Name:Gloucestershire Hospitals NHS Foundation Trust | ||
| Full Title: A study to research if foam sclerotherapy of saphenous trunks can speed up the healing of chronic venous leg ulcers | ||
| Medical condition: We will include patients with insufficiency of the long and/or short saphenous vein as underlying cause of their venous leg ulcer. These patients may or may not have visible varicose veins of the l... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-001855-37 | Sponsor Protocol Number: OCT02-2006 | Start Date*: 2007-05-14 | |||||||||||
| Sponsor Name:Schülke & Mayr GmbH | |||||||||||||
| Full Title: Effect of an octenidine-based topical antimicrobial agent (Octenisept) on wound healing of chronic venous leg ulcers: a prospective, twelve-week comparison versus local treatment with Ringer soluti... | |||||||||||||
| Medical condition: Chronic venous leg ulcers In Germany, approximately three million people suffer from chronic leg ulcers of various origins. These ulcers are often very painful and extremely cost-intensive disease... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) FR (Completed) HU (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-002332-16 | Sponsor Protocol Number: RC31-16-8917 | Start Date*: 2017-10-03 | |||||||||||
| Sponsor Name:Toulouse Hospital | |||||||||||||
| Full Title: Evaluation of the efficacy of injections of botulinic toxin in plantar lesions of patients suffering from localized epidermolysis bullosa simplex : double blind randomized controlled study. | |||||||||||||
| Medical condition: localized epidermolysis bullosa simplex | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-000202-20 | Sponsor Protocol Number: RC-P0041 | Start Date*: 2015-06-22 | |||||||||||||||||||||||||||||||
| Sponsor Name:Groupement des Hôpitaux de l’Institut Catholique de Lille (GHICL) | |||||||||||||||||||||||||||||||||
| Full Title: Effect and tolerance of ketamine's subcutaneous bolus during painful care, refractory of bedsore, ulcer, vascular wound care in palliative care units. | |||||||||||||||||||||||||||||||||
| Medical condition: Patients’ palliative care for bedsores, ulcers or vascular wounds, which are general characteristics of the patient population that will be included: usually elderly, undernourished and of multiple... | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2020-004940-27 | Sponsor Protocol Number: AIC316-03-II-01(Phase3) | Start Date*: 2022-01-05 |
| Sponsor Name:AiCuris Anti-infective Cures GmbH | ||
| Full Title: A randomized, open-label, multi-center, comparative trial, to assess the efficacy and safety of pritelivir versus foscarnet for the treatment of acyclovir-resistant mucocutaneous HSV infections in ... | ||
| Medical condition: Acyclovir-resistant mucocutaneous HSV infections in immunocompromised subjects | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) GR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
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Query did not match any studies.
