- Trials with a EudraCT protocol (38)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
38 result(s) found for: Accommodation.
Displaying page 1 of 2.
| EudraCT Number: 2010-021410-34 | Sponsor Protocol Number: EOC-2-Opht-2010 | Start Date*: 2010-08-12 | ||||||||||||||||
| Sponsor Name:Medical Centre Haaglanden | ||||||||||||||||||
| Full Title: A double blind randomized study on the efficacy of cyclopentolate 1% and cyclopentolate 1% with tropicamide 1% in children | ||||||||||||||||||
| Medical condition: Depth of cycloplegia; changes of astigmatism; recuperation from cycloplegia and mydriasis | ||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2008-003279-28 | Sponsor Protocol Number: LT2380-PII-11/07 | Start Date*: 2008-07-24 | |||||||||||||||||||||
| Sponsor Name:Laboratoires Théa | |||||||||||||||||||||||
| Full Title: Efficacy and safety assessment of intracameral T2380 (Fixed combination of lidocaïne, phenylephrine and tropicamide) for anaesthesia and mydriasis in phacoemulsification cataract surgery | |||||||||||||||||||||||
| Medical condition: The aim of the development was to develop a combination of active substances enabling to obtain at the same time a mydriasis and an anaesthesia during cataract surgery. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: FR (Ongoing) ES (Ongoing) BE (Completed) PT (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2009-017193-20 | Sponsor Protocol Number: S51994 | Start Date*: 2010-01-28 |
| Sponsor Name:UZLeuven | ||
| Full Title: Effect of naloxone and methylnaltrexone on satiety, gastric sensitivity, and accommodation to food in healthy volunteers. | ||
| Medical condition: healthy volunteers none; this is a physiological study to investigate the influence of opioid antagonism on gastric sensorimotor function | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-004862-89 | Sponsor Protocol Number: mirtazapine1 | Start Date*: 2015-02-16 |
| Sponsor Name:KULeuven | ||
| Full Title: The effect of mirtazapine (REMERGON®) on gastric motility and satiation in healthy subjects | ||
| Medical condition: Functional Dyspepsia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-002588-17 | Sponsor Protocol Number: SAM-IIT01 | Start Date*: 2019-10-21 |
| Sponsor Name:Universitätsklinikum Tübingen | ||
| Full Title: Safety and effects on visual function of 0.01% Atropin eye drops for myopia inhibition in children and adolescents | ||
| Medical condition: Myopia | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-004946-41 | Sponsor Protocol Number: s57223 | Start Date*: 2014-11-19 |
| Sponsor Name:KULeuven | ||
| Full Title: The influence of GLP-1 analog, liraglutide, on gastric accommodation, gastric emptying, hunger and the migrating motor complex in healthy volunteers | ||
| Medical condition: healthy volunteers no medical condition; drug will be studied because it is known to influence gastric motility | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-004180-13 | Sponsor Protocol Number: OCARINA | Start Date*: 2021-10-18 | ||||||||||||||||
| Sponsor Name:KU Leuven | ||||||||||||||||||
| Full Title: The effect of obeticholic acid on gut microbiota, gastric motility, accommodation, gastrointestinal peptide in healthy volunteers | ||||||||||||||||||
| Medical condition: The study will focus on the underlying mechanisms of gastrointestinal motility and gut microbiota in healthy subjects. | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2014-002092-28 | Sponsor Protocol Number: acotiamide1 | Start Date*: 2017-04-19 |
| Sponsor Name:KULeuven - TARGID | ||
| Full Title: The effect of acotiamide on gastric motility and satiation in healthy volunteers | ||
| Medical condition: Funtional gastroenterological disorder: Functional Dyspepsia more specific the postprandial distress syndrome. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-006082-88 | Sponsor Protocol Number: Rimonamaag | Start Date*: 2008-10-21 | |||||||||||
| Sponsor Name:UZLeuven | |||||||||||||
| Full Title: INFLUENCE OF RIMONABANT ON GASTRIC SENSITIVITY AND ON THE GASTRIC RESPONSE TO A MEAL 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 gastric sensorimotor function | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-021188-34 | Sponsor Protocol Number: LT2380-PIII-05/10 | Start Date*: 2011-07-01 | |||||||||||||||||||||
| Sponsor Name:Laboratoires Théa | |||||||||||||||||||||||
| Full Title: Efficacy and safety assessment of intracameral T2380 (Fixed combination of lidocaine, phenylephrine and tropicamide) for mydriasis and anaesthesia in phacoemulsification cataract surgery | |||||||||||||||||||||||
| Medical condition: The aim of this clinical study will be to develop a combination of active substances enabling to obtain at the same time a mydriasis and an anaesthesia during cataract surgery | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: PT (Completed) DE (Completed) BE (Completed) AT (Completed) ES (Ongoing) SE (Completed) IT (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2017-004108-23 | Sponsor Protocol Number: 17097AB-AS | Start Date*: 2018-10-09 |
| Sponsor Name:Belfast Health and Social Care Trust | ||
| Full Title: Low-dose atropine eye drops to reduce progression of myopia in children: a multi-centre placebo controlled randomised trial in the United Kingdom (CHAMP UK) | ||
| Medical condition: Myopia | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-003104-20 | Sponsor Protocol Number: Rimona2011 | Start Date*: 2011-10-06 |
| Sponsor Name:UZLeuven | ||
| Full Title: The effect of Acomplia® (rimonabant) on esophageal sensitivity and gastric accommodation during food intake in healthy volunteers: a single-blind, placebo-controlled study | ||
| Medical condition: study is conducted on healthy volunteers, no medical condition is investigated | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-023226-20 | Sponsor Protocol Number: S52711 | Start Date*: 2010-11-24 |
| Sponsor Name:KULeuven | ||
| Full Title: Effect of the GLP-1 analogue liraglutide on intragastric pressure and satiation during nutrient drink infusion. | ||
| Medical condition: healthy volunteers no medical condition; drugs will be studied because they are known to influence gastric motility. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-004192-41 | Sponsor Protocol Number: A0221109 | Start Date*: 2020-09-03 |
| Sponsor Name:Pfizer | ||
| Full Title: LONG-TERM EXTENSION STUDY TO EVALUATE THE SAFETY OF FESOTERODINE IN JAPANESE PEDIATRIC SUBJECTS WITH SYMPTOMS OF DETRUSOR OVERACTIVITY ASSOCIATED WITH A NEUROLOGICAL CONDITION (NEUROGENIC DETRUSOR ... | ||
| Medical condition: Urinary Bladder, Neurogenic | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2014-001864-36 | Sponsor Protocol Number: Rikkunshito1 | Start Date*: 2015-10-09 | |||||||||||
| Sponsor Name:uzleuven | |||||||||||||
| Full Title: A PLACEBO-CONTROLLED STUDY ON THE EFFECT OF RIKKUNSHITO ON GASTRIC ACCOMMODATION AND NUTRIENT TOLERANCE, QUANTIFIED BY INTRAGASTRIC PRESSURE MONITORING DURING INTRAGASTRIC NUTRIENT INFUSION, IN FUN... | |||||||||||||
| Medical condition: functional dyspepsia - postprandial distress syndrome | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002187-26 | Sponsor Protocol Number: neostigmine2019 | Start Date*: 2019-08-28 |
| Sponsor Name:KU Leuven - TARGID | ||
| Full Title: A Prospective evaluation of the effect of a single dose of neostigmine in patients with patients with weak or absent esophageal peristalsis | ||
| Medical condition: Patients with complaints of dysphagia and poor esophageal motility | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-000594-81 | Sponsor Protocol Number: S65020 | Start Date*: 2021-05-07 |
| Sponsor Name:University Hospitals Leuven (UZ Leuven) | ||
| Full Title: The effect of corticotropin release hormone on duodenal markers and gastric sensorimotor function in healthy volunteers | ||
| Medical condition: To assess the effect of the CRH on duodenal mast cell count, eosinophil count, immune activation, mucosal permeability and gastric sensorimotor function and gastrointestinal symptoms. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-002705-65 | Sponsor Protocol Number: PrucaloprideGastro1 | Start Date*: 2013-09-26 |
| Sponsor Name:TARGID | ||
| Full Title: The effect of Prucalopride (Resolor) on gastric motor function and gastric sensitivity | ||
| Medical condition: Functional dyspepsia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-004811-21 | Sponsor Protocol Number: s53584 | Start Date*: 2011-11-07 |
| Sponsor Name:UZLeuven | ||
| Full Title: The effect of Sildenafil citrate (Viagra ®) on stomach motility, gastric emptying and food intake in healthy volunteers | ||
| Medical condition: study is conducted on healthy volunteers, no medical condition is investigated | ||
| 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 | ||
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