- Trials with a EudraCT protocol (89)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (38)
89 result(s) found for: Burn.
Displaying page 1 of 5.
EudraCT Number: 2020-005865-14 | Sponsor Protocol Number: 2020110357 | Start Date*: 2021-04-20 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: Pain relief of methoxyflurane in patients with burns | |||||||||||||
Medical condition: Pain after burns | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003481-28 | Sponsor Protocol Number: RRK5108 | Start Date*: 2017-12-21 | ||||||||||||||||
Sponsor Name:University Hospitals Birmingham NHS Foundation Trust | ||||||||||||||||||
Full Title: A pilot randomised controlled trial to examine the efficacy and optimal dose of Acetic Acid to treat colonised burns wounds. | ||||||||||||||||||
Medical condition: Colonised burn wounds | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000996-26 | Sponsor Protocol Number: VAB1 | Start Date*: 2016-09-01 |
Sponsor Name:Region Ostergotland | ||
Full Title: Volumekinetics for hyperoncotic albumin in burn patients as well as for healthy subjects. | ||
Medical condition: Healthy adult volunteers and burn patients 3 to 10 Days after the injury. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000901-21 | Sponsor Protocol Number: 2013.03 | Start Date*: 2013-10-24 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Rode Kruis Ziekenhuis | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A randomized clinical trial on the effectiveness, cost-effectiveness and quality of life of Flaminal® versus Flammazine® in the treatment of superficial and deep partial thickness burns | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Patients with partial thickness burns and/ or mixed depth of partial and full thickness burns | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005115-17 | Sponsor Protocol Number: CS I-020502/02 | Start Date*: 2009-09-23 | |||||||||||||||||||||
Sponsor Name:Kuros Biosurgery AG | |||||||||||||||||||||||
Full Title: A phase 2b, multi-centre, randomized, intra-patient-controlled dose-finding study of I-020502 in patients undergoing autologous meshed skin grafting. | |||||||||||||||||||||||
Medical condition: acute wounds / deep partial and full thickness burns | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000147-31 | Sponsor Protocol Number: 19-211 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Clinical Evaluation Research Unit | |||||||||||||
Full Title: VItamin C in Thermal injuRY: The VICToRY Pilot Trial A feasibility study for a seamless adaptive phase II/III multi-center randomized trial | |||||||||||||
Medical condition: Severely burned patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000362-38 | Sponsor Protocol Number: BBW-11 | Start Date*: 2012-06-18 | |||||||||||
Sponsor Name:Birken AG | |||||||||||||
Full Title: Open, Blindly Evaluated, Prospective, Controlled, Randomized, Multicenter Phase III Clinical Trial to Compare Intra-individually the Efficacy and Tolerance of Oleogel-S10 versus Standard of Care in... | |||||||||||||
Medical condition: Superficial partial-thickness (grade 2a) burn wounds | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002870-27 | Sponsor Protocol Number: ASCAB | Start Date*: 2018-12-11 | |||||||||||
Sponsor Name:Dept. of Plastic Surgery and Burns Treatment, Copenhagen University Hospital Rigshospitalet | |||||||||||||
Full Title: Adipose-derived Stem Cells in the treatment of Acute Burns (ASCAB) | |||||||||||||
Medical condition: Skin burns. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003285-42 | Sponsor Protocol Number: PHT/2005/37 | Start Date*: 2005-11-28 |
Sponsor Name:Portsmouth Institution Medicine, Health & Social Care, Portsmouth University [...] | ||
Full Title: A RCT to test the analgesic efficacy of topical morphine on minor and partial thickness burns in A&E | ||
Medical condition: Minor superficial and partial thickness burns <5% body surface area. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000839-54 | Sponsor Protocol Number: SMi-MW-12 | Start Date*: 2012-06-07 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: The effect of late naloxon-infusion on secondary hyperalgesia after a first degree burn injury | |||||||||||||
Medical condition: Induced pain in volunteers | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015090-12 | Sponsor Protocol Number: 04082009 | Start Date*: 2013-07-23 | ||||||||||||||||
Sponsor Name:Association of Dutch Burn Centres | ||||||||||||||||||
Full Title: Standard Treatment Or topical doxepin against Pruritus in burn patients | ||||||||||||||||||
Medical condition: Pruritus in patients with burns | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004296-19 | Sponsor Protocol Number: NBS07.116 | Start Date*: 2008-02-07 | |||||||||||
Sponsor Name:Association of Dutch Burn Centres | |||||||||||||
Full Title: Application of cultured autologous keratinocytes in combination with a meshed split skin autograft for burn wound healing | |||||||||||||
Medical condition: Even standard treatment, transplantation with a (meshed) split skin autograft, does not result in satisfactory functional and cosmetic appearance of the healed wound. Due to limited available donor... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003662-41 | Sponsor Protocol Number: MW-2004-11-02 | Start Date*: 2005-11-24 |
Sponsor Name:MediWound Ltd | ||
Full Title: Enzymatic Debridement in Burns Patients (Children & Adults): A Comparison to Standard of Care (Protocol MW 2004-11-02) | ||
Medical condition: Burn wounds defined as deep partial thickness or full thickness thermal burns. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Completed) SK (Ongoing) PT (Completed) CZ (Completed) IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000897-38 | Sponsor Protocol Number: DAM/001/05 | Start Date*: 2005-05-18 | |||||||||||
Sponsor Name:FARMACEUTICI DAMOR | |||||||||||||
Full Title: Open-label, controlled, randomised, multicentre, parallel group clinical trial of efficacy and tolerability of Fitostimoline soaked gauzes, Fitostimoline cream and Citrizan gel in the topical... | |||||||||||||
Medical condition: Topical treatment of second-degree superficial cutaneous burns | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004304-12 | Sponsor Protocol Number: 2260/2006 | Start Date*: 2007-09-25 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA PISANA | |||||||||||||
Full Title: Pilot study, randomised, open-label, monocentre, case vs control study to assess the effect of topically and parenterally Heparin administration treatment in superficial and deep second grade bu... | |||||||||||||
Medical condition: Superficial and deep second degree burns. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005663-27 | Sponsor Protocol Number: HDNX | Start Date*: 2013-02-27 | |||||||||||
Sponsor Name:HOC, Rigshospitalet | |||||||||||||
Full Title: Effect of a late naloxone-infusion on secondary hyperalgesia after a first degree heat injury. | |||||||||||||
Medical condition: First degree burn injury in healthy volunteers | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003289-42 | Sponsor Protocol Number: 41399 | Start Date*: 2012-12-21 |
Sponsor Name:Academic Medical Center Amsterdam | ||
Full Title: Randomized Controlled Trial Investigating the Efficacy and Safety of Nebulized Heparin versus Placebo in Burn Patients with Inhalation Trauma | ||
Medical condition: Burn-associated inhalation trauma requiring intubation and mechanical ventilation. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004541-34 | Sponsor Protocol Number: 21092005 | Start Date*: 2006-02-14 |
Sponsor Name:South Manchester University Healthcare Trust | ||
Full Title: The Effect of Enteral Administration of Synbiotics Upon Infection Rates in Major Burns | ||
Medical condition: Major burn injuries: Thermal related trauma with burn injury involving significant proportions of the total body surface area, as defined by age: Adults (>=17 years old): >= 15% body surface area ... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2013-000057-44 | Sponsor Protocol Number: MW2008-09-03 | Start Date*: 2013-09-05 |
Sponsor Name:Mediwound Ltd | ||
Full Title: Feasibility Study: Enzymatic Debridement in Patients (Adults) with Partial Thickness and Full Thickness Burns - Protocol MW 2008-09-03 | ||
Medical condition: Eschar removal from partial thickness and full thickness burns | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-006182-32 | Sponsor Protocol Number: ANESBURN_1017 | Start Date*: 2009-06-03 |
Sponsor Name:Anaesthesiology Department. Universitary Hospital Vall d'Hebron, Barcelona. | ||
Full Title: Ensayo clínico controlado y aleatorizado para evaluar el efecto de los gabapentinoides sobre el dolor agudo postoperatorio en pacientes quemados | ||
Medical condition: Postoperative pain in burned patients with a burn excision area between 2 and 12 % of total body surface area. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
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