- Trials with a EudraCT protocol (18)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
18 result(s) found for: Anal Fissure.
Displaying page 1 of 1.
EudraCT Number: 2007-004114-13 | Sponsor Protocol Number: 956 | Start Date*: 2008-01-07 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: TOPIC LEVETIRACETAM IN ANAL FISSURE. A PILOT STUDY ABOUT EFFECTIVENESS AND TOLERABLENESS | |||||||||||||
Medical condition: Anal fissure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002656-42 | Sponsor Protocol Number: GTN 07 | Start Date*: 2008-03-27 | |||||||||||
Sponsor Name:SOFAR SPA | |||||||||||||
Full Title: Efficacy and tolerability of a 0.25%glyceryl trinitrate ointment in the treatment of chronic rectal fissures.A multicentric, randomised, open study,controlled vs. Antrolin cream. | |||||||||||||
Medical condition: chronic anal fissures | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001958-24 | Sponsor Protocol Number: DIL 05 | Start Date*: 2005-10-18 | |||||||||||
Sponsor Name:SOFAR SPA | |||||||||||||
Full Title: Efficacy and tolerability of Diltiazem cream in the treatment of chronic anal fissure: a prospective,randomized, double blind study versus glyceryl trinitrate. | |||||||||||||
Medical condition: Treatment of chronic anal fissures. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003931-63 | Sponsor Protocol Number: D-CAF-06 | Start Date*: 2007-02-19 | |||||||||||
Sponsor Name:S.L.A. Pharma (UK) Ltd | |||||||||||||
Full Title: A double-blind, placebo-controlled, randomised, multi-centre, dose-ranging study to determine the safety and efficacy of three concentrations of topical diltiazem cream in the treatment of chronic ... | |||||||||||||
Medical condition: Chronic anal fissure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005172-26 | Sponsor Protocol Number: D-AF-09 | Start Date*: 2010-09-06 | |||||||||||
Sponsor Name:S.L.A. Pharma (UK) Ltd | |||||||||||||
Full Title: A Randomised, Double-Blind, Placebo-Controlled Trial of the Safety and Efficacy of Diltiazem Hydrochloride Cream in Subjects with Anal Fissure | |||||||||||||
Medical condition: Symptomatic relief of pain related to anal fissure (AF). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) LT (Completed) ES (Completed) BG (Completed) SK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001216-11 | Sponsor Protocol Number: FISAN-BOT-2017-01 | Start Date*: 2017-04-25 |
Sponsor Name:Dra. A. Teresa Calderón Duque | ||
Full Title: Usefulness of botulinum toxin type A in the treatment of chronic anal fissure | ||
Medical condition: Chronic anal fissure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-018506-37 | Sponsor Protocol Number: NITRODIL-2010 | Start Date*: 2010-11-25 | |||||||||||
Sponsor Name:Mª Isabel Fernández García | |||||||||||||
Full Title: Ensayo clínico randomizado, de grupos paralelos para estudiar la eficacia y seguridad de diltiazem frente a nitroglicerina en pacientes con fisura anal. | |||||||||||||
Medical condition: Fisura anal | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003351-65 | Sponsor Protocol Number: RDD110 | Start Date*: 2016-03-16 |
Sponsor Name:RDD Pharma Ltd. | ||
Full Title: The Effect of Intra-anal Nifedipine, Used As Add-on to Conservative Therapy, on Pain in Patients with Anal Fissure | ||
Medical condition: Anal Fissure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BG (Completed) PL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000853-30 | Sponsor Protocol Number: DRGT119C01 | Start Date*: 2019-05-31 | |||||||||||
Sponsor Name:Druggability Technologies Holdings Ltd | |||||||||||||
Full Title: A Randomized, Double-Blind, Adaptive Trial with an Open-Label Treatment Extension to Determine the Efficacy and Safety of Topical DRGT-119 0.1% and 0.2% Gels in Patients with Chronic Anal Fissure | |||||||||||||
Medical condition: chronic anal fissure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002819-60 | Sponsor Protocol Number: FAC-BOTOX | Start Date*: 2021-08-19 |
Sponsor Name:Hospital Universitario de Burgos | ||
Full Title: Treatment of chronic anal fissure with ultrasound-guided intersphincteric infiltration of botulinum toxin A. | ||
Medical condition: Chronic anal fissure | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003627-54 | Sponsor Protocol Number: 150601 | Start Date*: 2016-05-11 | |||||||||||
Sponsor Name:Tecnimede, Sociedade Técnico-Medicinal, S.A. | |||||||||||||
Full Title: Randomized, multicenter, placebo-controlled, double blind study to assess the efficacy and tolerability of 2% diltiazem hydrochloride in the treatment of chronic anal fissure and a 24 week follow-u... | |||||||||||||
Medical condition: Cronic Anal fissure (CAF) The underlying pathogenesis of chronic anal fissure involves initial local trauma (generally caused by hard stools), resulting in a wound, internal anal sphincter spasm an... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005675-15 | Sponsor Protocol Number: DIL-UBI-DEX-CLOII/2003/003/PT | Start Date*: 2008-10-08 | |||||||||||
Sponsor Name:Tecnimede, Sociedade Técnico-Medicinal S.A. | |||||||||||||
Full Title: Randomized, multicenter, placebo-controlled, single blind study to assess the efficacy and tolerability of a combination of a cream containing ubidecarenone, dexpanthenol and chlorohexidine and a p... | |||||||||||||
Medical condition: Cronic Anal fissure (CAF) The underlying pathogenesis of chronic anal fissure involves initial local trauma (generally caused by hard stools), resulting in a wound, internal anal sphincter spasm an... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) CZ (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003753-28 | Sponsor Protocol Number: VEN307-AF-001 | Start Date*: 2013-09-09 |
Sponsor Name:Ventrus Biosciences | ||
Full Title: A Phase 3B, Randomized, Double-Blind, Placebo-controlled, Parallel-Treatment Group, Multicenter Efficacy and Safety Study of Topical Diltiazem Hydrochloride 2% Cream in subjects with Anal Fissure | ||
Medical condition: Pain associated with anal fissures | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PL (Completed) BG (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023538-22 | Sponsor Protocol Number: LY107 | Start Date*: 2011-08-30 |
Sponsor Name:Lipid Pharmaceuticals | ||
Full Title: Lýsi sem hægðalyf fyrir börn | ||
Medical condition: The primary objective of this trial is to investigate the laxative effect of Lysisstílar (Free Fatty Acids suppositories) as compared to Klyx. Participants are children aged 1 year old to 17 year... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: IS (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-002811-33 | Sponsor Protocol Number: LAINCO1107 | Start Date*: 2017-12-11 | |||||||||||
Sponsor Name:LAINCO S.A | |||||||||||||
Full Title: Unilateral, open and randomized phase IV study of 2 groups to assess the degree of comfort with simple Emuliquen® in patients undergoing proctological surgery | |||||||||||||
Medical condition: Surgery proctological | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003346-16 | Sponsor Protocol Number: 2012-01-ANE | Start Date*: 2017-02-16 |
Sponsor Name:Hospital Universitari Sagrat cor | ||
Full Title: Comparative study between continuous perfusion and split doses in the treatment of postoperative pain | ||
Medical condition: Analgesic efficacy in postoperative acute pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000245-12 | Sponsor Protocol Number: Repha_1436 | Start Date*: 2020-01-20 | ||||||||||||||||
Sponsor Name:Repha GmbH | ||||||||||||||||||
Full Title: Controlled clinical trial to evaluate the efficacy and safety of MYRRHINIL-INTEST® versus placebo in patients with diarrhea-dominant irritable bowel syndrome (IBS-D) and patients with mixed-type ir... | ||||||||||||||||||
Medical condition: A confirmed diagnosis of irritable bowel syndrome (IBS-D or IBS-M) by a specialist in gastroenterology and/or internal medicine and/or general medicine | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002072-92 | Sponsor Protocol Number: B5161002 | Start Date*: 2014-12-30 | |||||||||||
Sponsor Name:Pfizer Inc. 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A Phase 2 Randomized, Double-Blind, Placebo-Controlled, Multiple Ascending Dose Study to Evaluate The Safety, Efficacy, Pharmacokinetics and Pharmacodynamics of PF-06252616 In Ambulatory Boys With ... | |||||||||||||
Medical condition: Duchenne's Muscular Dystrophy | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male | ||||||||||||
Trial protocol: GB (Prematurely Ended) IT (Prematurely Ended) PL (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
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