- Trials with a EudraCT protocol (15)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
15 result(s) found for: Soap.
Displaying page 1 of 1.
EudraCT Number: 2014-004662-26 | Sponsor Protocol Number: LACAC_L_04298 | Start Date*: 2015-03-25 | |||||||||||
Sponsor Name:Sanofi | |||||||||||||
Full Title: Safety Dermatological Evaluation: genital Mucosa Irritation - Product tested: Dermacyd PH_DETINLYN Sweet Flower. | |||||||||||||
Medical condition: Healthy volunteers (hygiene) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004663-20 | Sponsor Protocol Number: LACAC_L_04301 | Start Date*: 2015-03-25 | |||||||||||
Sponsor Name:Sanofi | |||||||||||||
Full Title: Safety Dermatological Evaluation: genital mucosa irritation - Product tested: Dermacyd PH_DETINBACK Sweet Flower | |||||||||||||
Medical condition: Healthy volunteers (hygiene) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004665-24 | Sponsor Protocol Number: LACAC_L_04307 | Start Date*: 2015-03-25 | |||||||||||
Sponsor Name:Sanofi | |||||||||||||
Full Title: Safety Dermatological Evaluation: genital mucosa irritation - Product tested: Dermacyd PH_DETINBACK Tangerine Mix. | |||||||||||||
Medical condition: Healthy volunteers (hygiene) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005614-30 | Sponsor Protocol Number: SOAP2016 | Start Date*: 2016-07-07 |
Sponsor Name:Uzsoki Utcai Kórház | ||
Full Title: SOAP Antibiotic prophylaxis trial Systemic versus combined systemic and Oral Antibiotic Prophylaxis in elective colorectal surgery | ||
Medical condition: In colorectal surgery wildely used bowel prep and systemic antibiotic prophylaxis. New data suggest that infective complications can be lowered if beside this regimen oral antibiotic profilaxis is ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-022701-17 | Sponsor Protocol Number: 1709801154 | Start Date*: 2015-11-17 |
Sponsor Name:Isala | ||
Full Title: Reduction of surgical-site infection in hip and knee arthroplasty: the influence of perioperative mupirocin nasal ointment and chlorhexidine soap in a double-blind, randomized, multicentre, placebo... | ||
Medical condition: osteoarthritis of hip and knee, prevention of surgical site infections after arthroplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004660-37 | Sponsor Protocol Number: LACAC_L_03732 | Start Date*: 2015-03-25 | |||||||||||
Sponsor Name:Sanofi | |||||||||||||
Full Title: Monocentric Study, Phase III, for Safety Dermatological Evaluation: Acceptability With Gynecological Follow up - Dermacyd Tina Gel Sweet Flower | |||||||||||||
Medical condition: Healthy volunteers (hygiene) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004664-38 | Sponsor Protocol Number: LACAC_L_04304 | Start Date*: 2015-03-25 | |||||||||||
Sponsor Name:Sanofi | |||||||||||||
Full Title: Safety Dermatological Evaluation: genital mucosa irritation - Product tested: Dermacyd PH_DETINLYN Tangerine Mix. | |||||||||||||
Medical condition: Healthy volunteers (hygiene) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000777-38 | Sponsor Protocol Number: SOAP | Start Date*: 2014-06-19 | |||||||||||
Sponsor Name:Fondazione IRCCS Istituto Nazionale dei Tumori | |||||||||||||
Full Title: Activity and safety of second line SOrafenib After Pazopanib in patients with metastatic renal cell carcinoma (SOAP Study) | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005777-22 | Sponsor Protocol Number: MRSA-01 | Start Date*: 2009-04-07 |
Sponsor Name:Dermal Laboratories | ||
Full Title: Control of MRSA skin and wound colonisation. | ||
Medical condition: MRSA-colonised community patients with "uncomplicated" venous leg ulcers scheduled to receive regular nursing care, for 12 to 15 weeks, will be considered for the study. NB: There is no intention t... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-004998-83 | Sponsor Protocol Number: MUS92579_2057_1 | Start Date*: 2012-04-04 | |||||||||||
Sponsor Name:Merz Pharmaceuticals GmbH | |||||||||||||
Full Title: A Double-Blind, Randomized, Dose Selection Vehicle–Controlled Multicenter Clinical Study for Evaluation of the Safety, Tolerability, Efficacy, and Pharmacokinetics of topical Neramexane in Subjects... | |||||||||||||
Medical condition: Moderate to severe acne | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002666-47 | Sponsor Protocol Number: SOAP1 | Start Date*: 2017-11-02 | |||||||||||
Sponsor Name:Dpt. of Ophthalmology, Rigshospitalet-Glostrup | |||||||||||||
Full Title: Effect of drop-less surgery compared to topical NSAID alone and combination of steroid and NSAID on central macular thickness after cataract surgery, a randomized controlled trial | |||||||||||||
Medical condition: Postoperative cystoid macular edema following cataract surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001716-30 | Sponsor Protocol Number: CRC-ACNE-AC-04 | Start Date*: 2013-09-23 | |||||||||||
Sponsor Name:Clinical Research Center for Hair and Skin Science | |||||||||||||
Full Title: Exploratory, controlled, randomized, observer-blind intrainidividual clinical trial to evaluate the efficacy and the tolerability of topically applied 0.1% tyrothricin (Tyrosur® Gel) in patients wi... | |||||||||||||
Medical condition: MILD TO SEVERE PAPULOPUSTULAR ACNE | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001440-99 | Sponsor Protocol Number: ANB019-208 | Start Date*: 2021-08-25 | |||||||||||
Sponsor Name:AnaptysBio Inc. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Subjects with Hidradenitis Suppurativa | |||||||||||||
Medical condition: Hidradenitis Suppurativa | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002919-15 | Sponsor Protocol Number: CLS001-CO-PR-004 | Start Date*: 2015-11-16 | |||||||||||
Sponsor Name:Cutanea Life Sciences, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Vehicle-Controlled, Double-Blind, Multicenter Study to Evaluate the Safety and Efficacy of a Once-Daily CLS001 Topical Gel Versus Vehicle Administered for 12 Weeks to Subject... | |||||||||||||
Medical condition: Papulopustular rosacea | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) NL (Ongoing) SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002920-23 | Sponsor Protocol Number: CLS001-CO-PR-005 | Start Date*: 2015-12-18 | |||||||||||
Sponsor Name:Cutanea Life Sciences, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Vehicle-Controlled, Double-Blind, Multicenter Study to Evaluate the Safety and Efficacy of Once-Daily CLS001 Topical Gel Versus Vehicle Administered for 12 Weeks to Subjects ... | |||||||||||||
Medical condition: Papulopustular Rosacea | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) NL (Ongoing) SE (Completed) | |||||||||||||
Trial results: (No results available) |
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