- Trials with a EudraCT protocol (192)
 - Paediatric studies in scope of Art45 of the Paediatric Regulation (27)
 
		
	   		
	   		    
                    
                   	
                   	    192 result(s) found for: Constipation.
                    
                
			
   			
		
		Displaying page 1 of 10.
	
	
	| 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: 2005-006111-47 | Sponsor Protocol Number: SC03005 | Start Date*: 2006-03-27 | |||||||||||
| Sponsor Name:McNeil Ltd | |||||||||||||
| Full Title: A double-blind, randomised, parallel group pilot study to compare macrogol 3350 + electrolytes versus placebo in the overnight relief of constipation | |||||||||||||
| Medical condition: Constipation | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 2007-007610-10 | Sponsor Protocol Number: 11500005 | Start Date*: 2009-01-13 | |||||||||||
| Sponsor Name:UMC Utrecht | |||||||||||||
| Full Title: Prevention of constipation during treatment with opioids: magnesiumoxide versus macrogol/elektrolytes | |||||||||||||
| Medical condition: Palliative care cancer patients starting with opioids | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-002900-15 | Sponsor Protocol Number: Transidose-GE_01/2013 | Start Date*: 2014-04-28 | |||||||||||
| Sponsor Name:Salsarulo Pharma | |||||||||||||
| Full Title: Clinical trial to evaluate the efficacy and safety of oral Transidose in patients suffering from constipation. | |||||||||||||
| Medical condition: Constipation | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 2018-001914-13 | Sponsor Protocol Number: MACR001 | Start Date*: 2018-10-08 | |||||||||||
| Sponsor Name:Salsarulo Pharma | |||||||||||||
| Full Title: Clinical Trial to Evaluate the Efficacy and Safety of MACRORANGE® in Patients Suffering from Functional Constipation | |||||||||||||
| Medical condition: Functional constipation | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-004293-26 | Sponsor Protocol Number: QTM/GEP0512 | Start Date*: 2013-09-03 | |||||||||||
| Sponsor Name:GeiserPHARMA SL | |||||||||||||
| Full Title: Multisite, open, randomized, parallel and controlled clinical trial, to evaluate the efficacy and safety of a laxative fiber formula compared to Plantaben on objective and subjective parameters of ... | |||||||||||||
| Medical condition: Occasional constipation | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-001991-34 | Sponsor Protocol Number: 122.56 | Start Date*: 2007-08-15 | |||||||||||
| Sponsor Name:Boehringer Ingelheim Limited | |||||||||||||
| Full Title: A randomised, double-blind, placebo-controlled, parallel group study to assess the efficacy and safety of 4 weeks treatment with bisacodyl (Dulcolax®) tablets 10 mg administered orally, once daily,... | |||||||||||||
| Medical condition: This randomised, double-blind, placebo-controlled, parallel group trial will be conducted in patients with functional constipation | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-001985-16 | Sponsor Protocol Number: D3820C00006 | Start Date*: 2011-09-09 | ||||||||||||||||
| Sponsor Name:AstraZeneca AB | ||||||||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of NKTR-118 in Relieving Opioid-Induced Constipation (OIC) in Patients with Cancer-Related Pain. | ||||||||||||||||||
| Medical condition: Scientific Terminology Opioid-Induced Constipation (OIC) Laymen Terminology Constipation after taking Opioid drugs | ||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SK (Completed) DE (Completed) ES (Completed) BE (Completed) GB (Completed) CZ (Completed) HU (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2009-011853-42 | Sponsor Protocol Number: NALCOL 01 | Start Date*: 2009-12-22 | |||||||||||
| Sponsor Name:Norfolk and Norwich University Hospital NHS Trust | |||||||||||||
| Full Title: NALOXONE HYDROCHLORIDE SR GASTRO-RESISTANT SUSTAINED RELEASE CAPSULES AS A TREATMENT FOR FUNCTIONAL CONSTIPATION: A RANDOMISED, DOUBLE BLIND CONTROLLED TRIAL IN SECONDARY CARE | |||||||||||||
| Medical condition: Functional constipation | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-005961-77 | Sponsor Protocol Number: 3200K1-3357-WW | Start Date*: 2009-05-06 | |||||||||||
| Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc. | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study of Subcutaneous MOA-728 for the Treatment of Opioid-Induced Constipation Estudio multicéntrico, aleatorizado, en do... | |||||||||||||
| Medical condition: Opioid-induced constipation in subjects with non-malignant pain Tratamiento del estreñimiento inducido por opiáceos en sujetos con dolor de origen no maligno | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-005935-14 | Sponsor Protocol Number: 3200K1-3358-WW | Start Date*: 2009-04-24 | |||||||||||
| Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc. | |||||||||||||
| Full Title: An Open-Label Study to Evaluate the Long-term Safety of Subcutaneous MOA-728 for Treatment of Opioid-Induced Constipation in Subjects With Nonmalignant Pain Estudio abierto para evaluar la segurida... | |||||||||||||
| Medical condition: Opioid-induced constipation in subjects with non-malignant pain Tratamiento del estreñimiento inducido por opiáceos en sujetos con dolor de origen no maligno | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-001986-41 | Sponsor Protocol Number: D3820C00005 | Start Date*: 2012-02-21 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of NKTR-118 in Patients with Non-Cancer-Related Pain and Opioid-Induced Constipation (OIC) | |||||||||||||
| Medical condition: Opioid-induced constipation (OIC) | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) HU (Completed) CZ (Completed) BE (Completed) ES (Completed) SE (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 (Completed) | ||||||||||||||||||
| 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: 2019-001955-38 | Sponsor Protocol Number: LIN-MD-66 | Start Date*: 2021-05-10 | ||||||||||||||||
| Sponsor Name:Allergan Ltd | ||||||||||||||||||
| Full Title: A Phase 3, Open-label, Long-term Safety Study of Oral Linaclotide Administered to Pediatric Participants with Functional Constipation (FC) or Irritable Bowel Syndrome with Constipation (IBS-C) | ||||||||||||||||||
| Medical condition: Functional Constipation (FC) Irritable bowel syndrome with constipation (IBS-C) | ||||||||||||||||||
					
						
							
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: HU (Prematurely Ended) BG (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| 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: 2010-022402-40 | Sponsor Protocol Number: M0001-C303 | Start Date*: 2011-05-05 | |||||||||||
| Sponsor Name:Shire-Movetis NV | |||||||||||||
| Full Title: Trial consisting of an 8-week double-blind placebo-controlled part to evaluate efficacy, safety, tolerability and pharmacokinetics of prucalopride in paediatric subjects with functional constipatio... | |||||||||||||
| Medical condition: Functional constipation in paediatric subjects | |||||||||||||
					
						
							
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) NL (Completed) FR (Completed) GB (Completed) DE (Completed) HU (Completed) PL (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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) | |||||||||||||
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