- Trials with a EudraCT protocol (6)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
6 result(s) found for: dermapro.
Displaying page 1 of 1.
EudraCT Number: 2012-005841-19 | Sponsor Protocol Number: DT-DP-D3 | Start Date*: 2013-10-10 | |||||||||||
Sponsor Name:DermaTools Biotech GmbH | |||||||||||||
Full Title: A Multicentric, Double Blind, randomised, Comparative Phase III Study of the Efficacy of the new Wound Healing Solution Diperoxochloric acid (DPOCL, DermaPro®) compared to isotonic Sodium Chloride ... | |||||||||||||
Medical condition: Diabetic foot ulcers with mean diameter between 1.5 and 5 cm after débridement (if indicated); wound stage Wagner grade I or II, Armstrong stadium A or C (for Wagner-Armstrong-Classification), trea... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) LV (Completed) LT (Completed) HU (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020437-12 | Sponsor Protocol Number: DT-DP-D2b | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:DermaTools Biotech GmbH | |||||||||||||
Full Title: A multicentric, double blind, randomized, comparative Phase II b study of the efficacy of a wound healing solution in patients with diabetic foot ulcer | |||||||||||||
Medical condition: diabetic foot ulcer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) LV (Prematurely Ended) LT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004527-67 | Sponsor Protocol Number: DT-DP-DFU-CR-04 | Start Date*: 2018-08-06 |
Sponsor Name:DermaTools Biotech GmbH | ||
Full Title: A Randomised Dose Finding Study Comparing The Safety And Efficacy Of three blinded doses of Diperoxochloric Acid (DPOCl, DermaPro®) and A Standard Moist Wound Dressing In Patients With Non-Healing... | ||
Medical condition: Diabetic foot ulcer with mean diameter between 1.5 and 4 cm after débridement if indicated), Wound stage Wagner grade I or II, Armstrong stadium A or C (for Wagner-Armstrong-Classification), tr... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: LV (Completed) EE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-007748-85 | Sponsor Protocol Number: DT-DP-D02 | Start Date*: 2008-06-26 | ||||||||||||||||||||||||||
Sponsor Name:DermaTools Biotech GmbH | ||||||||||||||||||||||||||||
Full Title: A Prospective, Randomized, Open Label, Add-On, Parallel Arm, In-Patient Comparison Phase II Study to Evaluate the Safety and Efficacy of Diperoxochloric Acid (DermaPro®) in Wounds with Impaired Hea... | ||||||||||||||||||||||||||||
Medical condition: Wounds with Impaired Healing | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003326-23 | Sponsor Protocol Number: DT-DP-DFU-CR-05 | Start Date*: 2021-07-05 |
Sponsor Name:DermaTools Biotech GmbH | ||
Full Title: A Prospective, Randomized, Double-Blind, Vehicle-Controlled Study To Evaluate The Safety and Efficacy of Diperoxochloric Acid (DPOCl, DermaPro®) In Patients With Non-Healing Diabetic Foot Ulcers | ||
Medical condition: 3. Diabetic foot ulcer treated unsuccessfully for at least 4 weeks with mean diameter between 1.5 and 4 cm after débridement | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) LV (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-001001-40 | Sponsor Protocol Number: DT-DP-UC-CR-01 | Start Date*: 2014-06-13 |
Sponsor Name:DermaTools Biotech GmbH | ||
Full Title: A multicentre, double-blind, randomised, controlled phase II/III study to evaluate the efficacy and safety of the new wound healing solution Diperoxochloric acid (DPOCl, DermaPro®) in patients with... | ||
Medical condition: Venous leg ulcer (ulcus cruris) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: LV (Prematurely Ended) LT (Prematurely Ended) | ||
Trial results: (No results available) |
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