- Trials with a EudraCT protocol (83)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
83 result(s) found for: Sphincter.
Displaying page 1 of 5.
EudraCT Number: 2008-004858-33 | Sponsor Protocol Number: Version 2.0 (03Nov2010) | Start Date*: 2009-01-09 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: Open label pilot study to treat women with chronic urinary retention or voiding dysfunction due to a primary disorder of sphincter relaxation (Fowler’s syndrome) with outpatient urethral sphincter ... | |||||||||||||
Medical condition: Primary abnormality of the urethral sphincter or Fowlers Syndrome | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003759-11 | Sponsor Protocol Number: FI 1 | Start Date*: 2007-03-09 |
Sponsor Name:BKH Schwaz | ||
Full Title: Autologous myoblasts for treatment of anal incontinence due to anal sphincter defects | ||
Medical condition: Fecal (anal) inconinence caused by ruptures/ traumas of the external anal sphincter | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000563-16 | Sponsor Protocol Number: Citalopram2016 | Start Date*: 2016-06-09 |
Sponsor Name:K.U. Leuven | ||
Full Title: Effect of citalopram on fasting and postprandial lower esophageal sphincter function in healthy subjects: a double-blind, placebo-controlled, randomized, cross-over study | ||
Medical condition: Increased lower esophageal sphincter pressure | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-000532-17 | Sponsor Protocol Number: Methylnaltrexone2016 | Start Date*: 2016-06-09 |
Sponsor Name:K.U. Leuven | ||
Full Title: Effect of methylnaltrexone on intragastric pressure, the occurrence of transient lower esophageal sphincter relaxations and reflux events in healthy subjects: a double-blind, placebo-controlled, ra... | ||
Medical condition: Impaired gastric accommodation | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-004239-63 | Sponsor Protocol Number: NL68231.078.18 | Start Date*: 2019-08-23 | |||||||||||
Sponsor Name:Erasmus MC | |||||||||||||
Full Title: Botulinum toxin (BOTOX®) to prevent post-operative pancreatic fistula in patients who undergo distal pancreatectomy. PROFIT study. | |||||||||||||
Medical condition: Post-operative pancreatic fistula | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002335-27 | Sponsor Protocol Number: IGG-VIJA-001 | Start Date*: 2005-09-01 | |||||||||||
Sponsor Name:ISTITUTO GIANNINA GASLINI | |||||||||||||
Full Title: Botulin Toxin injection for the treatment of Internal Anal Sphincter Achalasia | |||||||||||||
Medical condition: Treatment of internal anal sphincter achalasia | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002882-19 | Sponsor Protocol Number: MCHT001 | Start Date*: 2004-12-10 |
Sponsor Name:Mid Cheshire Hospitals NHS Trust | ||
Full Title: A controlled trial into the benefit of topical perianal glyceryl trinitrate (GTN) as a sphincter relaxant, pre-insertion of ultrasound probe for trans rectal ultrasound (TRUS) guided biopsy of the ... | ||
Medical condition: Prostate Cancer Diagnosis – Pain relief during biopsy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004139-23 | Sponsor Protocol Number: 62202-677 | Start Date*: 2006-08-18 |
Sponsor Name:University of Cologne | ||
Full Title: An open-label, non-randomized phase I/II trial of neoadjuvant radio-immunochemotherapy with cetuximab and 5-FU for advanced rectal cancer | ||
Medical condition: advanced adenocarcinoma of the rectum | ||
Disease: | ||
Population Age: | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2015-000419-42 | Sponsor Protocol Number: Nalogexol-2014 | Start Date*: 2015-05-11 | |||||||||||
Sponsor Name:Aalborg University Hospital | |||||||||||||
Full Title: Naloxegol and assessments of opioid induced bowel dysfunction | |||||||||||||
Medical condition: Healthy volunteers (Opioid-induced bowel dysfunction) | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001384-12 | Sponsor Protocol Number: PancolonicPressurization | Start Date*: 2014-07-16 |
Sponsor Name:KULEUVEN | ||
Full Title: IS THE ABSENCE OF PAN-COLONIC PRESSURIZATIONS A RELEVANT PATHOPHYSIOLOGICAL MECHANISM IN A SUBGROUP OF PATIENTS WITH CHRONIC IDIOPHATIC CONSTIPATION? | ||
Medical condition: COLONIC MOTILITY WILL BE STUDIED BOTH IN HEALTHY SUBJECTS AND IN PATIENTS WITH CHRONIC CONSTIPATION | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-021463-32 | Sponsor Protocol Number: IC-01-02-02-007 | Start Date*: 2011-02-24 | |||||||||||
Sponsor Name:Innovacell Biotechnologie AG | |||||||||||||
Full Title: Skeletal muscle-derived cell implantation for the treatment of fecal incontinence: a multicenter, randomized, double-blind, placebocontrolled, parallel-group, dose-finding clinical study | |||||||||||||
Medical condition: Fecal incontinence in female and male patients with external anal sphincter weakness or sphincter damage. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) DE (Prematurely Ended) SE (Prematurely Ended) CZ (Prematurely Ended) GB (Prematurely Ended) SI (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004501-25 | Sponsor Protocol Number: D9120C00020 | Start Date*: 2006-12-18 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A double-blind, placebo controlled, randomized, two centre phase IIa pharmacodynamic cross-over study to assess the effect of AZD3355, 65 mg bid, on transient lower esophageal sphincter relaxations... | |||||||||||||
Medical condition: Gastroesophageal Reflux Disease (GERD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001371-38 | Sponsor Protocol Number: EMR 62202-688 | Start Date*: 2006-08-31 |
Sponsor Name:Institute of Oncology Ljubljana | ||
Full Title: Cetuximab (Erbitux®), capecitabine and radiotherapy in neoadjuvant treatment of patients with locally advanced resectable rectal cancer: A phase II Pilot Study | ||
Medical condition: Locally advanced, resectable stage II/III rectal cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SI (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-003582-10 | Sponsor Protocol Number: AVANA | Start Date*: 2019-01-17 | |||||||||||
Sponsor Name:G.O.N.O. - GRUPPO ONCOLOGICO DEL NORD OVEST | |||||||||||||
Full Title: PHASE II STUDY OF PREOPERATIVE CHEMORADIOTHERAPY PLUS AVELUMAB IN PATIENTS WITH LOCALLY ADVANCED RECTAL CANCER | |||||||||||||
Medical condition: Locally advanced rectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000649-20 | Sponsor Protocol Number: STAR-03 | Start Date*: 2012-06-11 | |||||||||||
Sponsor Name:FONDAZIONE DELL'ISTITUTO TOSCANO TUMORI | |||||||||||||
Full Title: Phase II study of pre-operative treatment with external radiotherapy plus panitumumab in operable locally advanced rectal cancer (favourable and intermediate prognostic group) (RaP Study/STAR-03) | |||||||||||||
Medical condition: Operable locally advanced rectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001178-28 | Sponsor Protocol Number: FISPAC-2011 | Start Date*: 2012-09-05 |
Sponsor Name:Fundación para la Investigación Biomédica del Hospital Universitario La Paz | ||
Full Title: Multicentre, randomized, comparative and Add-on, in two parallel groups to assess the efficacy and safety of autologous mesenchymal stem cells derived from expanded adipose tissue (ASC) for the tre... | ||
Medical condition: Local treatment in complex perianal fistulas in patients without inflammatory bowel disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (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: 2008-006081-29 | Sponsor Protocol Number: Rimonaslok | Start Date*: 2008-10-21 | |||||||||||
Sponsor Name:UZLeuven | |||||||||||||
Full Title: INFLUENCE OF RIMONABANT ON LOWER ESOPHAGEAL FUNCTION IN HEALTHY VOLUNTEERS | |||||||||||||
Medical condition: none; this is a physiological study to investigate the influence of CB1 receptor antagonism by rimonabant (normally used for the treatment of obesity) on esophageal function, i.e. esophageal contr... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004672-35 | Sponsor Protocol Number: 09-025 | Start Date*: 2014-05-13 | ||||||||||||||||
Sponsor Name:Cook Myosite, Incorporated | ||||||||||||||||||
Full Title: A Prospective Nonrandomized Study of Autologous Muscle Derived cell (AMDC) Transplantation for Treatment of Fecal Incontinence | ||||||||||||||||||
Medical condition: Fecal incontinence in men and women | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-006310-13 | Sponsor Protocol Number: CAO/ARO/AIO-12 | Start Date*: 2015-01-19 | ||||||||||||||||
Sponsor Name:University Hospital Frankfurt, Goethe University | ||||||||||||||||||
Full Title: CAO/ARO/AIO-12: Induction chemotherapy before or after preoperative chemoradiotherapy and surgery for locally advanced rectal cancer: A randomized phase II trial of the German Rectal Cancer Study ... | ||||||||||||||||||
Medical condition: Locally advanced rectal cancer (UICC stage II and III) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
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