- Trials with a EudraCT protocol (855)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
		
	   		
	   		    
                    
                   	
                   	    855 result(s) found for: Medication compliance.
                    
                
			
   			
		
		Displaying page 1 of 43.
	
	
	| EudraCT Number: 2005-000374-48 | Sponsor Protocol Number: 104325 | Start Date*: 2005-05-25 | 
| Sponsor Name:GlaxoSmithKline Pharma A/S | ||
| Full Title: A randomized, open label comparative study to determine the proportion of asthma patients on Seretide Diskus 50/250 mcg b.i.d. achieving total control when given medication and compli-ance enhancem... | ||
| Medical condition: Asthma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-003987-35 | Sponsor Protocol Number: Metamizole001 | Start Date*: 2015-11-10 | 
| Sponsor Name:JESSA Hospital | ||
| Full Title: Metamizole versus NSAID at home after ambulatory surgery: a double-blind randomized controlled trial | ||
| Medical condition: Pain after ambulatory surgery | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-000307-32 | Sponsor Protocol Number: Repha_1439 | Start Date*: 2020-05-12 | |||||||||||
| Sponsor Name:Repha GmbH | |||||||||||||
| Full Title: Clinical trial for examination of efficacy and safety of MYRRHINIL-INTEST® versus placebo in patients with diarrhea-dominant irritable bowel syndrom (IBS-D) | |||||||||||||
| Medical condition: Confirmed diagnosis of diarrhea-dominant irritable bowel syndrome (IBS-D) by a specialist physician 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: 2014-005418-45 | Sponsor Protocol Number: HCQCVDRASLE-1.1 | Start Date*: 2015-05-04 | 
| Sponsor Name:Christine Bengtsson [...] | ||
| Full Title: Improved cardiovascular risk factors and inflammatory markers in Rheumatoid Arthritis and Systemic Lupus Erythematosus? New aspects of Hydroxychloroquine – an interventional study (HCQCVDRASLE) | ||
| Medical condition: Rheumatoid Arthritis and Systemic Lupus Erythematosus | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-004836-31 | Sponsor Protocol Number: Tav01-13 | Start Date*: 2014-04-07 | 
| Sponsor Name:Montavit Ges.m.b.H. | ||
| Full Title: Double-blind, randomised, placebo-controlled study evaluating the efficacy and safety of Tavipec capsules in acute Bronchitis A prsopective, multi-centre, parallel group, interventional clinical ph... | ||
| Medical condition: acute bronchitis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-004473-16 | Sponsor Protocol Number: SL001-2.0 | Start Date*: 2016-07-19 | 
| Sponsor Name:Masarykův onkologický ústav | ||
| Full Title: Prospective study investigating efficacy of lanreotide on decrease of chemotherapy induced diarrhoea (CID) in patiens with colorectal carcinoma. | ||
| Medical condition: Chemotherapy induced diarrhoea that is resistant to common treatment including loperamide in patients with colorectal carcinoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-002977-23 | Sponsor Protocol Number: Tav02-13 | Start Date*: 2013-12-13 | 
| Sponsor Name:Montavit Ges.m.b.H. | ||
| Full Title: Double-blind, randomised, placebo-controlled study evaluating the efficacy and Safety of Tavipec® capsules in acute Rhinosinusitis A prospective, multi-centre, parallel group, interventional clinic... | ||
| Medical condition: Acute Rhinosinusitis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) PL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2022-001184-28 | Sponsor Protocol Number: PeP-RALP | Start Date*: 2022-10-11 | 
| Sponsor Name:Oslo University Hospital | ||
| Full Title: Perioperative Propranolol in Robotic Assisted Laparoscopic Prostatectomy - A Pilot Study A parallel-group, phase 2, double-blind, 2-arm study to assess the feasibility of conducting a formal large... | ||
| Medical condition: Prostate Cancer | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: NO (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-003716-91 | Sponsor Protocol Number: CGB-1108 | Start Date*: 2023-02-21 | |||||||||||
| Sponsor Name:Centrum Gastroenterologie Bethanien | |||||||||||||
| Full Title: Randomized controlled clinical trial to evaluate the efficacy of alginates in washout of proton pump inhibitor therapy with consideration of compliance and symptom burden in patients with gastroeso... | |||||||||||||
| Medical condition: Randomized controlled clinical trial to evaluate the efficacy of alginates in washout of proton pump inhibitor therapy with consideration of compliance and symptom burden in patients with gastroeso... | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-005265-11 | Sponsor Protocol Number: GWMS0501 | Start Date*: 2006-04-03 | 
| Sponsor Name:GW Pharma Ltd | ||
| Full Title: A double blind, randomised, placebo controlled, parallel group study of Sativex® when added to the existing treatment regimen, in the relief of central neuropathic pain in subjects with multiple sc... | ||
| Medical condition: Relief of central neuropathic pain in subjects with multiple sclerosis (MS) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) CZ (Completed) FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-001098-26 | Sponsor Protocol Number: MK-7264-034 | Start Date*: 2018-09-21 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
| Full Title: A Phase 2a, Proof of Concept, Randomized, Double-blind, Placebo-controlled Clinical Trial, to Evaluate the Efficacy and Safety of MK-7264 in Women with Moderate to Severe Endometriosis-related Pain | |||||||||||||
| Medical condition: Moderate to severe Endometriosis-related pain (ERP) | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: ES (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003407-34 | Sponsor Protocol Number: pre-CIN | Start Date*: 2021-06-01 | 
| Sponsor Name:Oslo University Hospital | ||
| Full Title: A randomized clinical three-arm trial comparing inflammation and cystoid macular edema for the medication regimens preoperative and postoperative topical NSAIDs to only postoperative topical NSAIDs... | ||
| Medical condition: Cataract surgery, and the medical treatment is anti-inflammatory eye drops to treat (and prevent) intraocular inflammation and development og cystoid macular edema. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-004029-87 | Sponsor Protocol Number: KCL/PCT-CT2004-1 | Start Date*: 2005-01-24 | 
| Sponsor Name:Institute of Psychiatry | ||
| Full Title: Pillot randomised controlled trial of antidepressant switching for treatmetn-refractory depression in primary care | ||
| Medical condition: Depression | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-003002-27 | Sponsor Protocol Number: MIT-Es001-C303 | Start Date*: 2020-10-14 | |||||||||||
| Sponsor Name:Estetra SRL | |||||||||||||
| Full Title: A Multicenter, Open-label, Single-Arm Study to Evaluate the Safety, Compliance and Pharmacokinetics associated with the use of a Combined Oral Contraceptive Containing 15 mg Estetrol monohydrate an... | |||||||||||||
| Medical condition: Contraception | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adolescents, Under 18 | Gender: Female | ||||||||||||
| Trial protocol: FI (Completed) EE (Completed) LV (Completed) SE (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-002177-11 | Sponsor Protocol Number: 80-83600-98-20013 | Start Date*: 2015-04-16 | 
| Sponsor Name:ZonMW GGG | ||
| Full Title: Step-down versus step-up analgesics in patients with (sub)acute sciatica in primary care | ||
| Medical condition: Patients with (sub)acute sciatica in primary care. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-001669-35 | Sponsor Protocol Number: 19139A | Start Date*: 2021-02-01 | 
| Sponsor Name:H. Lundbeck A/S (Lundbeck) | ||
| Full Title: Interventional, randomized, double-blind, parallel-group, placebo-controlled study to evaluate the efficacy and safety of eptinezumab for the preventive treatment of migraine in patients with a dua... | ||
| Medical condition: Preventive treatment of migraine in patients with a dual diagnosis of migraine and Medication Overuse Headache | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-004192-37 | Sponsor Protocol Number: CRO1749 | Start Date*: 2012-04-24 | |||||||||||
| Sponsor Name:Joint Research Compliance Office, Imperial College | |||||||||||||
| Full Title: Hellenic Anglo Research into Morning Or Night antihypertensive drug deliverY trial. | |||||||||||||
| Medical condition: Hypertension | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-002962-11 | Sponsor Protocol Number: IQUO/01 | Start Date*: 2013-05-24 | 
| Sponsor Name:Interessenverband zur Qualitätsicherung der Arbeit niedergelassener Uro-Onkologen in Deutschland (IQUO) e.V. | ||
| Full Title: Optimizing Pazopanib Exposure in RCC Patients through Therapeutic Drug Monitoring Followed by Intrapatient Dose Escalation | ||
| Medical condition: Renal cell carcinoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-003676-70 | Sponsor Protocol Number: PedPreMed | Start Date*: 2016-05-13 | 
| Sponsor Name:Norrbottens läns landsting | ||
| Full Title: Preanesthetic medication in pediatric patients: A comparison of midazolam, clonidine and dexmedetomidine | ||
| Medical condition: Is there a difference in anxiety- and sedation-level, and in anesthesia induction compliance between the preanesthetics included in study, in pediatric patients? Can we prevent and reduce anxiety w... | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: SE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-000619-85 | Sponsor Protocol Number: 2937 | Start Date*: 2005-05-25 | 
| Sponsor Name:The University of Liverpool [...] | ||
| Full Title: The relationship between genetic polymorphisms in the organic cation transporter genes and the pharmacokinetics and pharmacodynamics of metformin | ||
| Medical condition: Type 2 diabetes mellitus | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
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