- Trials with a EudraCT protocol (312)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (5)
		
	   		
	   		    
                    
                   	
                   	    312 result(s) found for: Balance.
                    
                
			
   			
		
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	| EudraCT Number: 2004-002108-14 | Sponsor Protocol Number: PD-BLS-01-EU | Start Date*: 2005-06-22 | 
| Sponsor Name:Fresenius Medical Care Deutschland GmbH. | ||
| Full Title: Multizentrische Studie mit einer Niedrig-Natrium Peritonealdialyse-Lösung bei hypertensiven od. antihypertensiv behandelten CAPD Patienten auf balance Lösung | ||
| Medical condition: | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-000562-21 | Sponsor Protocol Number: L00014 CP 201 | Start Date*: 2007-09-19 | |||||||||||
| Sponsor Name:PIERRE FABRE MEDICAMENT - IDPF | |||||||||||||
| Full Title: Effects of TANGANIL (three 500 mg tablets twice daily) on postural disturbances in the elderly. | |||||||||||||
| Medical condition: Postural disturbances in the elderly | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-001545-25 | Sponsor Protocol Number: CHDR1409 | Start Date*: 2014-07-02 | ||||||||||||||||
| Sponsor Name:Centre for Human Drug Research | ||||||||||||||||||
| Full Title: Randomized, double-blind, placebo-controlled, three way crossover, double dummy, single centre study evaluating the effect of haloperidol 2 mg and lorazepam 1 mg on posturography and underlying sys... | ||||||||||||||||||
| Medical condition: Healthy volunteers (balance disorders) | ||||||||||||||||||
| 
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| Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2016-004176-22 | Sponsor Protocol Number: IMPURE-Study | Start Date*: 2017-04-28 | 
| Sponsor Name:Medizinische Universität Graz | ||
| Full Title: IMProving Ultrafiltration and REmoval of uremic toxins by adapted automated peritoneal dialysis in a single center study (IMPURE-Study). | ||
| Medical condition: Chronic kidney disease G5D | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-003184-11 | Sponsor Protocol Number: R0002820 | Start Date*: 2016-01-04 | 
| Sponsor Name:Radboud University Medical Centre | ||
| Full Title: Functional effects of botulinum toxin in the hip adductors and subsequent exercise in patients with hereditary spastic paraplegia: a pilot RCT | ||
| Medical condition: Hereditary Spastic Paraplegia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-005324-17 | Sponsor Protocol Number: JH01 | Start Date*: 2007-04-13 | 
| Sponsor Name:Sint Maartenskliniek | ||
| Full Title: Influence of indometacin on reaction time, postural balance and obstacle avoidance in healthy subjects. | ||
| Medical condition: Healthy volunteers trial with registered NSAID. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-003365-99 | Sponsor Protocol Number: NL62809.068.17 | Start Date*: 2017-11-08 | 
| Sponsor Name:Maastricht University | ||
| Full Title: The effects of ceasing opioid, benzodiazepine, or Z-hypnotic drug use on measures of driving performance and postural balance. | ||
| Medical condition: Insomnia, Anxiety, chronic pain | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-002568-18 | Sponsor Protocol Number: 5B | Start Date*: 2015-07-15 | 
| Sponsor Name:Stockholm County Council, Karolinska University Hospital Huddinge, Department of Anesthesiology and Intensive Care | ||
| Full Title: Albumin mass balance and kinetics in liver transplantation. An open exploratory pilot study | ||
| Medical condition: liver transplantation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-001104-41 | Sponsor Protocol Number: ALXN1840-WD-204 | Start Date*: 2020-07-22 | |||||||||||
| Sponsor Name:Alexion Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Phase 2, open-label study to assess copper and molybdenum balance in participants with Wilson disease treated with ALXN1840 | |||||||||||||
| Medical condition: Wilson Disease (WD) | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-002011-61 | Sponsor Protocol Number: 77267 | Start Date*: 2021-08-13 | 
| Sponsor Name:Academisch ziekenhuis Maastricht | ||
| Full Title: The glutamate/GABA balance as novel therapeutic target for psychotic and cognitive symptoms in 22q11.2 deletion syndrome | ||
| Medical condition: 22q11.2 deletion syndrome | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-004627-20 | Sponsor Protocol Number: 176S11NB | Start Date*: 2013-04-05 | |||||||||||
| Sponsor Name:Pascoe pharmazeutische Präparate GmbH | |||||||||||||
| Full Title: Randomized double-blind, placebo controlled study with NEURAPAS® balance in addition to psychoeducation or psychotherapy in adolescents from 12 to 17 years suffering from mild depressive episodes w... | |||||||||||||
| Medical condition: Mild depressive episodes with nervous restlessness | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-005129-99 | Sponsor Protocol Number: TA799-013 | Start Date*: 2021-02-10 | |||||||||||
| Sponsor Name:VectivBio AG | |||||||||||||
| Full Title: A multicenter, open-label, metabolic balance study to evaluate the effects of apraglutide on intestinal absorption in adult subjects with short bowel syndrome, intestinal failure (SBS-IF), and colo... | |||||||||||||
| Medical condition: short bowel syndrome, intestinal failure (SBS-IF), colon-in-continuity (CIC) | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) BE (Completed) DK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-003781-42 | Sponsor Protocol Number: 17465 | Start Date*: 2005-09-21 | 
| Sponsor Name:University of Dundee | ||
| Full Title: | ||
| Medical condition: Transient hypothyroxinanaemia | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-002404-42 | Sponsor Protocol Number: 17465 | Start Date*: 2005-08-18 | 
| Sponsor Name:University of Dundee | ||
| Full Title: A pilot study to inform a randomised controlled trial of iodine supplementation in preterm infants | ||
| Medical condition: transient hypothyroxinaemia | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-004466-34 | Sponsor Protocol Number: 005,1 | Start Date*: 2014-02-25 | 
| Sponsor Name:Hyks Silmätautien klinikka | ||
| Full Title: The effect of hypertonic saline on blood electrolytes, acid-base balance and hormones that regulate blood pressure | ||
| Medical condition: Elevated intraocular pressure | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-005734-18 | Sponsor Protocol Number: VOLU-011-CP4 | Start Date*: 2012-07-23 | 
| Sponsor Name:Fresenius Kabi Deutschland GmbH | ||
| Full Title: Prospective randomised controlled open-label explorative multi-centre pilot trial of Volulyte®-supplemented versus Albumin-supplemented fluid resuscitation for major burns | ||
| Medical condition: patients with major burns | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-012073-34 | Sponsor Protocol Number: R0000063 | Start Date*: 2009-07-08 | |||||||||||
| Sponsor Name:Radboud University Nijmegen Medical Centre | |||||||||||||
| Full Title: Botulinum toxin for treating calf muscle spasticity in Hereditary Spastic Paraparesis (HSP): functional effects on dynamic balance and gait | |||||||||||||
| Medical condition: Subjects with hereditary spastic paraparesis (HSP) | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-001762-13 | Sponsor Protocol Number: sepsis 1 | Start Date*: 2005-07-13 | 
| Sponsor Name:Universitätskinderklinik Heidelberg | ||
| Full Title: Energy metabolism of critically ill children treated with lipid emulsion and carnitine | ||
| Medical condition: The primary purpose of the study is an examination of the ability of lipid emulsions and carnitin supplementation to reduce the morbidity associated with sepsis and catabolic conditions by altering... | ||
| Disease: | ||
| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-001317-15 | Sponsor Protocol Number: BAL2-2006 | Start Date*: 2006-05-09 | 
| Sponsor Name:University of Oxford | ||
| Full Title: BALANCE 2: Bipolar disorder:Antidepressant/Lamotrigine/ANtipsychotic Comparative Evaluation | ||
| Medical condition: Bipolar depression. | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-002487-41 | Sponsor Protocol Number: GLY-321-2017 | Start Date*: 2018-01-31 | |||||||||||
| Sponsor Name:GLyPharma Therapeutic Inc. (a wholly owned subsidiary of VectivBio Holding AG) | |||||||||||||
| Full Title: A Phase Ib/IIa open-label, repeated dose, metabolic balance study of FE 203799 in patients with short bowel syndrome | |||||||||||||
| Medical condition: Short bowel syndrome (SBS) | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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