- Trials with a EudraCT protocol (74)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
74 result(s) found for: Chronic Constipation.
Displaying page 1 of 4.
EudraCT Number: 2006-001896-39 | Sponsor Protocol Number: DUO 05 | Start Date*: 2006-12-07 | |||||||||||
Sponsor Name:SOFAR SPA | |||||||||||||
Full Title: Evaluation of symbiotic effect on the intestinal function in idiopathic chronic constipation. Multicenter, randomised, cross-over, double-blind, placebo-controlled study | |||||||||||||
Medical condition: CIdiopathic chronic constipation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010945-30 | Sponsor Protocol Number: 110309 | Start Date*: 2010-03-15 | |||||||||||
Sponsor Name:UNIVERSITA` DEGLI STUDI DI NAPOLI FEDERICO II | |||||||||||||
Full Title: Prospective, Randomized, Controlled, Double Blind Study on the Effectiveness of Movicol (PEG 3350) versus SedaStip (acacia fiber, psyllium fiber (Plantago ovata), fructose) in the Treatment of Chro... | |||||||||||||
Medical condition: constipation | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001676-36 | Sponsor Protocol Number: 3066001 | Start Date*: 2007-12-18 | |||||||||||
Sponsor Name:ORION PHARMA | |||||||||||||
Full Title: Non-inferiority study; Comparison of polyethylene glycol solution with and without electrolytes for treatment of chronic constipation in elderly institutionalised patients: a double-blind, randomis... | |||||||||||||
Medical condition: Constipation | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015943-17 | Sponsor Protocol Number: ONCO_PAIN01/2009 | Start Date*: 2010-04-23 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | ||||||||||||||||||
Full Title: SEQUENTIAL STUDY ON THE INCIDENCE AND INTENSITY OF INTESTINAL CONSTIPATION ASSOCIATED TO OXYCODONE (OXYCONTIN) AND THE COMBINATION OF OXYCODONE/NALOXONE (TARGIN) FOR CHRONIC ONCOLOGIC PAIN TREATMEN... | ||||||||||||||||||
Medical condition: Advanced neoplastic desease with pain | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000913-30 | Sponsor Protocol Number: Nath1/2008 | Start Date*: 2008-10-13 | |||||||||||
Sponsor Name:NATHURA SRL | |||||||||||||
Full Title: A symbiotic for the treatment of functional constipation | |||||||||||||
Medical condition: Functional crhonic constipation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002145-21 | Sponsor Protocol Number: 2007003 | Start Date*: 2007-12-21 | |||||||||||
Sponsor Name:Procter & Gamble Pharmaceuticals | |||||||||||||
Full Title: A Phase II, Randomized, Placebo-controlled Study of ATI-7505 in Patients with Chronic Idiopathic Constipation | |||||||||||||
Medical condition: Chronic Idiopathic Constipation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) BE (Completed) GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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: 2011-000670-62 | Sponsor Protocol Number: M0001-C401(SPD555-C401) | Start Date*: 2011-05-26 | |||||||||||
Sponsor Name:Shire-Movetis NV | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled trial to evaluate the efficacy, quality of life, safety and tolerability of long-term treatment (24 weeks) with prucalopride in subjects aged ≥18 year... | |||||||||||||
Medical condition: Chronic constipation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Completed) HU (Completed) SE (Completed) IT (Completed) ES (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004384-31 | Sponsor Protocol Number: SAG/0211PFC-11S1 | Start Date*: 2015-06-10 | |||||||||||
Sponsor Name:Sucampo AG | |||||||||||||
Full Title: A Multicentre, Long-term Safety, Efficacy and Pharmacokinetics Study of Lubiprostone in Paediatric Subjects Aged ≥6 to <18 years with Functional Constipation | |||||||||||||
Medical condition: functional constipation in paediatric patients | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) DE (Completed) ES (Ongoing) NL (Completed) FR (Ongoing) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005601-46 | Sponsor Protocol Number: 000081 | Start Date*: 2013-05-15 | |||||||||||
Sponsor Name:Ferring International Pharmascience Center US, Inc. | |||||||||||||
Full Title: A Multicenter, Open-label, Safety and Tolerability Extension Trial of 5 mg and 10 mg Elobixibat Daily in the Treatment of Chronic Idiopathic Constipation | |||||||||||||
Medical condition: Chronic idiopathic constipation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) SE (Completed) SK (Completed) HU (Completed) CZ (Completed) GB (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015652-20 | Sponsor Protocol Number: M0001-C301/SPD555-301 | Start Date*: 2010-05-10 | |||||||||||
Sponsor Name:Shire-Movetis NV | |||||||||||||
Full Title: A 12-week, randomised, double-blind, placebo-controlled trial to evaluate the efficacy and safety of prucalopride in subjects with chronic non-cancer pain suffering from opioid induced constipation | |||||||||||||
Medical condition: opioid induced constipation in subjects with chronic non-cancer pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) PL (Prematurely Ended) DE (Prematurely Ended) CZ (Completed) FR (Completed) NL (Prematurely Ended) BG (Prematurely Ended) GB (Prematurely Ended) ES (Prematurely Ended) HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015719-42 | Sponsor Protocol Number: M0001-C302 | Start Date*: 2010-08-12 | |||||||||||
Sponsor Name:Shire-Movetis NV | |||||||||||||
Full Title: A 12-week, randomised, double-blind, placebo controlled trial to evaluate the efficacy, quality of life, safety and tolerability of prucalopride in male subjects with chronic constipation | |||||||||||||
Medical condition: Chronic constipation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) CZ (Completed) GB (Completed) FR (Completed) NL (Completed) BG (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000821-30 | Sponsor Protocol Number: SAD13-ER1 | Start Date*: 2013-07-12 |
Sponsor Name:Enrique Rey Díaz-Rubio | ||
Full Title: CLINICAL RESPONSE TO 5HT4 RECEPTORS AGONIST (PRUCALOPRIDE): GASTROCOLIC REFLEX | ||
Medical condition: chronic constipation | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002949-11 | Sponsor Protocol Number: 1326V9235 | Start Date*: 2014-02-11 | |||||||||||
Sponsor Name:Shionogi Inc. | |||||||||||||
Full Title: A Randomized Double-blind, Placebo-controlled, Parallel-group, Multicenter, Phase 3 Study to Evaluate the Long-term Safety of Naldemedine for the Treatment of Opioid-induced Constipation in Subje... | |||||||||||||
Medical condition: Opioid-induced Constipation in Subjects with Non-malignant Chronic Pain Receiving Opioid Therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) SE (Completed) BE (Completed) EE (Completed) PT (Completed) HU (Completed) AT (Completed) DK (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005111-32 | Sponsor Protocol Number: ABO-MELI-15 | Start Date*: 2016-02-24 | |||||||||||
Sponsor Name:ABOCA S.P.A. SOCIETà AGRICOLA | |||||||||||||
Full Title: Multicenter, Prospective, Comparative, Randomized Controlled Clinical investigation on the performance of Promelaxin® micro-enemas versus oral administration of Macrogol 4000, in the treatment of c... | |||||||||||||
Medical condition: Chronic Functional Constipation | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003468-30 | Sponsor Protocol Number: SAG/0211PFC-1131 | Start Date*: 2014-09-24 | |||||||||||
Sponsor Name:Sucampo Pharma Europe Ltd. | |||||||||||||
Full Title: A Multicentre, Randomised, Placebo-controlled, Double-blinded Study of the Efficacy, Safety, and Pharmacokinetics of Lubiprostone in Paediatric Subjects Aged ≥ 6 Years to < 18 Years with Functional... | |||||||||||||
Medical condition: functional constipation in paediatric patients | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) DE (Completed) ES (Prematurely Ended) NL (Completed) PL (Completed) FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002948-91 | Sponsor Protocol Number: 1315V9232 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Shionogi Inc. | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Parallel-group Study of Naldemedine in the Treatment of Opioid-induced Constipation in Subjects with Non-malignant Chronic Pain Receiving Opioid Therapy | |||||||||||||
Medical condition: Opioid-induced Constipation in Subjects with Non-malignant Chronic Pain Receiving Opioid Therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) AT (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023958-36 | Sponsor Protocol Number: 2011_HV_M2 | Start Date*: 2011-09-02 | ||||||||||||||||
Sponsor Name:Mª Antònia Perelló Juan | ||||||||||||||||||
Full Title: Ensayo clínico aleatorizado de fase IV, en secuencia cruzada, doble ciego, comparando la influencia de la flora intestinal productora del gas metano en la respuesta al tratamiento del estreñimiento... | ||||||||||||||||||
Medical condition: Estreñimiento crónico funcional | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005587-94 | Sponsor Protocol Number: 000079 | Start Date*: 2013-05-12 | |||||||||||
Sponsor Name:Ferring International Pharmascience Center US, Inc. | |||||||||||||
Full Title: A Double-blind, Randomised, Placebo-controlled, Phase 3 Trial in Patients with Chronic Idiopathic Constipation to Demonstrate the Efficacy and Safety of Elobixibat 5 mg and 10 mg for 26 Weeks | |||||||||||||
Medical condition: Chronic idiopathic constipation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Prematurely Ended) CZ (Prematurely Ended) GB (Completed) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002241-11 | Sponsor Protocol Number: 1314V9231 | Start Date*: 2014-03-10 | |||||||||||
Sponsor Name:Shionogi Inc. | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Parallel-group Study of Naldemedine in the Treatment of Opioid-induced Constipation in Subjects with Non-malignant Chronic Pain Receiving Opioid Therapy | |||||||||||||
Medical condition: Opioid-induced Constipation in Subjects with Non-malignant Chronic Pain Receiving Opioid Therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) CZ (Completed) GB (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
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