- Trials with a EudraCT protocol (59)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (57)
59 result(s) found for: Atropine.
Displaying page 1 of 3.
| EudraCT Number: 2021-004015-11 | Sponsor Protocol Number: MAD2021-07 | Start Date*: 2022-11-11 |
| Sponsor Name:Erasmus MC | ||
| Full Title: Investigator led, double-masked, multicenter, randomized clinical trial for the comparison of Atropine 0.5% versus Atropine 0.05% eye drops for the prevention of myopia progression in Dutch children. | ||
| Medical condition: Myopia | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-003340-37 | Sponsor Protocol Number: PJ21069 | Start Date*: 2018-10-30 | |||||||||||
| Sponsor Name:Technological University Dublin | |||||||||||||
| Full Title: Efficacy and Mechanisms of Low Dose Atropine in the Control of Myopia in Children Trial name: Myopia Outcome Study of Atropine in Children (MOSAIC) | |||||||||||||
| Medical condition: Myopia- a refractive error due to a discrepancy between the anatomical axial length and the focal length of the eye. resulting in distant objects appearing blurred | |||||||||||||
|
|||||||||||||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-002533-10 | Sponsor Protocol Number: SuRe-001 | Start Date*: 2013-05-22 |
| Sponsor Name:UMCG | ||
| Full Title: Comparison of the effects of atropine on haemodynamics and tissue oxygenation in anaesthesia with propofol and sufentanil versus propofol and remifentanil’ | ||
| Medical condition: Comparison of the effects of atropine on haemodynamics and tissue oxygenation in anaesthesia with propofol and sufentanil versus propofol and remifentanil | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-004884-29 | Sponsor Protocol Number: PSt012021 | Start Date*: 2022-03-16 |
| Sponsor Name:Pharma Stulln GmbH | ||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled Dose Finding Study of 0.05%, 0.025%, 0.01% and 0.005% Atropine Eye Drops to inhibit myopia progression in children in a European population | ||
| Medical condition: Myopia progression in children | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-001575-33 | Sponsor Protocol Number: P001307 | Start Date*: 2021-06-17 |
| Sponsor Name:Universitätsklinikum Freiburg | ||
| Full Title: Low-dose AtropIne for Myopia control in children | ||
| Medical condition: Myopia control in children. | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-001077-24 | Sponsor Protocol Number: CP-NVK002-0001 | Start Date*: 2019-07-10 | |||||||||||
| Sponsor Name:Vyluma Inc. | |||||||||||||
| Full Title: CHAMP: A 3-Arm Randomized, Double-Masked, Placebo-Controlled, Phase 3 Study of NVK-002 in Children with Myopia | |||||||||||||
| Medical condition: To treat the progression of myopia in children | |||||||||||||
|
|||||||||||||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Completed) GB (GB - no longer in EU/EEA) HU (Completed) NL (Completed) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-001286-16 | Sponsor Protocol Number: APP-study | Start Date*: 2018-11-05 | |||||||||||
| Sponsor Name:Rigshospitalet | |||||||||||||
| Full Title: Low-dose Atropine for the Prevention of Childhood Myopia Progression in Danish Children (APP-study) | |||||||||||||
| Medical condition: Childhood myopia | |||||||||||||
|
|||||||||||||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Restarted) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-002535-28 | Sponsor Protocol Number: 7343 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Hôpitaux Universitaires de Strasbourg | ||
| Full Title: Braking effect on myopia with atropine eye drops at 0.01%. | ||
| Medical condition: Myopia | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: FR (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-002046-16 | Sponsor Protocol Number: MARS_2020 | Start Date*: 2020-11-04 |
| Sponsor Name:Fakultní nemocnice Brno | ||
| Full Title: A Randomised, double-blinded, placebo-controlled, multicenter study of efficacy, safety and side effects of highly diluted atropine collyrium in slowing the progression of myopia (shortsightedness)... | ||
| Medical condition: Myopia in children | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: CZ (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-002834-36 | Sponsor Protocol Number: Retro-001 | Start Date*: 2012-09-13 |
| Sponsor Name:UMCG | ||
| Full Title: Evaluation of the effects of the addition of atropine during propofol/remifentanil induction of anesthesia on hemodynamics, microvascular blood flow and tissue oxygenenation in patients undergoing ... | ||
| Medical condition: ophthalmic surgery | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| 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: 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: 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: 2007-003017-14 | Sponsor Protocol Number: 132998 | Start Date*: 2008-01-08 |
| Sponsor Name:Käkkliniken, Universitetssjukhuset i Linköping | ||
| Full Title: A comparison of the effect of Atropine and Botulinum-toxin in patients with severe drooling | ||
| Medical condition: Patients with ALS, Parkinson´s disease, brain-damage cerebral paralysis or other neurological conditions often have an impaired swallowing, resulting in drooling. This adds a social handicap and o... | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-003976-42 | Sponsor Protocol Number: OT_101_001 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Ocumension (Hong Kong) Limited | ||
| Full Title: A phase III, randomized, double-masked, placebo controlled, parallel-group, multicenter study of the safety and efficacy of OT-101 (Atropine 0.01%) in treating the progression of myopia in pediatri... | ||
| Medical condition: myopia | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) SK (Ongoing) IE (Ongoing) HU (Ongoing) ES (Ongoing) PL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-003373-64 | Sponsor Protocol Number: 01-DIMS-2021 | Start Date*: 2021-11-22 |
| Sponsor Name:NOEMI GUEMES VILLAHOZ | ||
| Full Title: POST-MARKETING PARALLEL CLINICAL TRIAL TO DETERMINE THE EFFECTIVENESS AND TOLERABILITY OF DIMS LENSES IN THE CONTROL OF MYOPIA IN PEDIATRIC POPULATION | ||
| Medical condition: MYOPIA IN PEDIATRIC POPULATION | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-004775-13 | Sponsor Protocol Number: SYD-101-001 | Start Date*: 2019-08-02 | |||||||||||
| Sponsor Name:Sydnexis, Inc. | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-Masked, Vehicle-Controlled Study to Assess the Safety and Efficacy of SYD-101 Ophthalmic Solution for the Treatment of Myopia in Children | |||||||||||||
| Medical condition: Myopia | |||||||||||||
|
|||||||||||||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Trial now transitioned) AT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-000401-50 | Sponsor Protocol Number: CT-PED-2010-01 | Start Date*: 2011-08-09 | |||||||||||
| Sponsor Name:Fundación para la Formación e Investigación Sanitarias de la Región de Murcia | |||||||||||||
| Full Title: Efficacy and safety of reversal with Sugammadex (BRIDION®) from deep Neuromuscular Blockade induced by rocuronium in children | |||||||||||||
| Medical condition: Neuromuscular Blockade induced by Rocuronium | |||||||||||||
|
|||||||||||||
| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-003182-34 | Sponsor Protocol Number: 2018-10 | Start Date*: 2018-10-18 |
| Sponsor Name:CHR d'ORLEANS | ||
| Full Title: Randomized, double-blind, controlled clinical trial for comparison of continuous phenylephrine versus norepinephrine infusion for maintenance of hemodynamic stability during cesarean section under... | ||
| Medical condition: hypotension during caesarean section under spinal anesthesia | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-004082-33 | Sponsor Protocol Number: erythstom2 | Start Date*: 2011-10-05 |
| Sponsor Name:UZLeuven | ||
| Full Title: The role of induced phase 3 contractions in the control of hunger and food intake | ||
| Medical condition: Gastrointestinal contractility will be studied in healthy volunteers for 7 hours in a fasting condition | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
| Download Options: | |
|---|---|
| Number of Trials to download: | |
| Download Content: | |
| Download Format: | |
| Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. | |
Query did not match any studies.
