- Trials with a EudraCT protocol (730)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
730 result(s) found for: Secondary Hypertension AND Hypertension.
Displaying page 9 of 37.
EudraCT Number: 2018-001727-39 | Sponsor Protocol Number: POP03 | Start Date*: 2018-10-16 | ||||||||||||||||
Sponsor Name:Polpharma S.A. | ||||||||||||||||||
Full Title: A PHASE III, MULTICENTRE, RANDOMISED, INVESTIGATOR-MASKED, CROSSOVER, COMPARATIVE, NON-INFERIORITY TRIAL EVALUATING THE EFFICACY AND TOLERABILITY OF GENERIC LATANOPROST 0.05 MG/ML EYE DROPS SOLUTIO... | ||||||||||||||||||
Medical condition: Ocular hypertension and open angle glaucoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-004307-14 | Sponsor Protocol Number: BECRO/ACT/LATANOS | Start Date*: 2021-02-12 | ||||||||||||||||
Sponsor Name:actrevo GmbH | ||||||||||||||||||
Full Title: Non-inferiority, Randomized, Observer-blind, two Parallel Group, Clinical Trial for Comparing the Efficacy and Tolerability of a new Generic BAC-free Formulation of Latanoprost 0.05 mg/mL eye drops... | ||||||||||||||||||
Medical condition: Open angle glaucoma or ocular hypertension Elevated IOP and paediatric glaucoma. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-002844-24 | Sponsor Protocol Number: H6D-MC-LVGX | Start Date*: 2006-04-10 |
Sponsor Name:Lilly ICOS LLC | ||
Full Title: A Double-Blind, Extension Study to Evaluate the Long-Term Safety and Efficacy of the Phosphodiesterase Type 5 (PDE5) Inhibitor Tadalafil in the Treatment of Patients with Pulmonary Arterial Hyperte... | ||
Medical condition: Pulmonary arterial hypertension (PAH) is a chronic and progressive disease characterised by elevation of pulmonary artery pressure and pulmonary vascular resistance, leading to right heart failure ... | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Completed) IE (Completed) BE (Completed) ES (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-003387-27 | Sponsor Protocol Number: 848300145/0129/1POP04 | Start Date*: 2021-11-02 | ||||||||||||||||
Sponsor Name:Pharmaceutical Works Polpharma S.A. (Polpharma S. A.) | ||||||||||||||||||
Full Title: A PHASE III, MULTICENTRE, RANDOMISED, INVESTIGATOR-MASKED, CROSS-OVER, COMPARATIVE, NON-INFERIORITY TRIAL OF GENERIC LATANOPROST + TIMOLOL (50μG + 5MG)/ML EYE DROPS, SOLUTION (POLPHARMA S.A.) COMPA... | ||||||||||||||||||
Medical condition: Ocular hypertension and open angle glaucoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-005008-16 | Sponsor Protocol Number: STOPPIT-01 | Start Date*: 2021-03-08 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:University Medical Center Hamburg-Eppendorf | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Stop of proton-pump inhibitor treatment in patients with liver cirrhosis – a double-blind, placebo-controlled trial | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Liver cirrhosis | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003060-25 | Sponsor Protocol Number: MEIN/22/NeRam-Hyp/001 | Start Date*: 2023-03-07 | |||||||||||
Sponsor Name:Menarini International Operations Luxembourg SA | |||||||||||||
Full Title: Open-label, multicenter, multinational, interventional Clinical Trial to assess Efficacy and Safety of the extemporaneous combination of Nebivolol and Ramipril in hypertensive patients - ARTEMISIA ... | |||||||||||||
Medical condition: Cardiovascular Disease Hypertensive patients | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003816-21 | Sponsor Protocol Number: RDG-10298 | Start Date*: 2012-01-11 | ||||||||||||||||
Sponsor Name:S.A. Alcon-Couvreur N.V | ||||||||||||||||||
Full Title: Multi-Center Study Assessing Efficacy and Tolerability of TRAVATAN® Solution without BAK, containing Polyquad® Preservative (0.004% travoprost) in Patients Previously on latanoprost 0.005% or bimat... | ||||||||||||||||||
Medical condition: Open angle Glaucoma Ocular Hypertension | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) SE (Completed) ES (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-024332-42 | Sponsor Protocol Number: BAY63-2521/13605 | Start Date*: 2014-04-10 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled phase II study to investigate the efficacy and safety of riociguat (0.5 mg, 1.0 mg, 1.5 mg, 2.0 mg and 2.5 mg TID) in patients with symptomatic pulmon... | |||||||||||||
Medical condition: pulmonary hypertension associated with idiopathic interstitial pneumonias | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) DE (Completed) ES (Completed) BE (Completed) GB (Completed) PT (Completed) DK (Completed) GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003186-24 | Sponsor Protocol Number: 192024-092 | Start Date*: 2015-04-23 | |||||||||||||||||||||
Sponsor Name:Allergan Limited | |||||||||||||||||||||||
Full Title: The Efficacy and Safety of Bimatoprost SR in Patients With Open-angle Glaucoma or Ocular Hypertension | |||||||||||||||||||||||
Medical condition: Open-angle Glaucoma and Ocular Hypertension | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) CZ (Completed) DE (Trial now transitioned) IT (Completed) NL (Completed) PT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-019483-37 | Sponsor Protocol Number: PelleLindqvist | Start Date*: 2011-04-06 | |||||||||||||||||||||
Sponsor Name:Karolinska University Hospital | |||||||||||||||||||||||
Full Title: Vitamin D supplementation for prevention of placenta mediated pregnancy complications. | |||||||||||||||||||||||
Medical condition: We will try to prevent preeclampsia, groth restriction and prematurity by vitamin D supplementation given as one dose in mid pregnancy | |||||||||||||||||||||||
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Population Age: | Gender: Female | ||||||||||||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000774-70 | Sponsor Protocol Number: CVEA489A2302 | Start Date*: 2006-09-04 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: An 8-week, multicenter, randomized, double-blind, parallel-group study to evaluate the efficacy and safety of the combination of valsartan/HCTZ/amlodipine compared to valsartan/HCTZ, valsartan/amlo... | ||
Medical condition: Hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) SE (Completed) DK (Completed) PT (Completed) GR (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-001544-26 | Sponsor Protocol Number: RASCOVID-19 | Start Date*: 2020-04-22 | ||||||||||||||||
Sponsor Name:Center for Clinical Metabolic Research, Gentofte Hospital | ||||||||||||||||||
Full Title: Effects of discontinuing renin-angiotensin system inhibitors in patients with and without COVID-19 | ||||||||||||||||||
Medical condition: Coronavirus disease 2019 (COVID-19) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011157-41 | Sponsor Protocol Number: LT2345-PIII-12/08 | Start Date*: 2009-07-24 | ||||||||||||||||
Sponsor Name:laboratoires théa | ||||||||||||||||||
Full Title: Efficacy and Safety assessment of T2345 unpreserved eyedrops versus Xalatan® in ocular hypertensive or glaucomatous patients. Phase III study, multicentre, international, randomised, investigator-m... | ||||||||||||||||||
Medical condition: The study population is suffering from glaucoma. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) BE (Completed) ES (Completed) PT (Completed) IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002750-38 | Sponsor Protocol Number: C-08-09 | Start Date*: 2008-10-22 | |||||||||||||||||||||
Sponsor Name:Alcon Research Ltd | |||||||||||||||||||||||
Full Title: 24-hour IOP control with Travoprost / Brinzolamide fixed combination once-daily (QD)in the evening vs TRAVATAN | |||||||||||||||||||||||
Medical condition: Open-angle glaucoma or ocular hypertension | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-005091-42 | Sponsor Protocol Number: 192024-041D | Start Date*: 2012-05-08 | |||||||||||||||||||||
Sponsor Name:Allergan Limited | |||||||||||||||||||||||
Full Title: An Open Label (Stage 1) and Randomized (Stage 2), 24-Month Study of Safety and Efficacy of Bimatoprost Drug Delivery System in Patients With Open-Angle Glaucoma or Ocular Hypertension | |||||||||||||||||||||||
Medical condition: open-angle glaucoma (OAG) and ocular hypertension (OHT) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003423-21 | Sponsor Protocol Number: IK-7002-COPD-006 | Start Date*: 2014-09-29 | |||||||||||||||||||||||||||||||
Sponsor Name:Bellerophon Pulse Technologies LLC | |||||||||||||||||||||||||||||||||
Full Title: An Exploratory, Two-Part, Clinical Study to Assess the Effect of Pulsed, Inhaled Nitric Oxide (iNO) on Functional Pulmonary Imaging Parameters in Subjects with World Health Organization (WHO) Group... | |||||||||||||||||||||||||||||||||
Medical condition: Part 1: Pulmonary Hypertension (PH) Associated with Chronic Obstructive Pulmonary Disease (COPD) Part 2: Pulmonary Hypertension (PH) Associated with Idiopathic pulmonary fibrosis (IPF) | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-022984-36 | Sponsor Protocol Number: 201051 | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||
Sponsor Name:Santen Oy | ||||||||||||||||||||||||||||
Full Title: A phase III, randomized, double-masked 6-month clinical study to compare the efficacy and safety of the preservative-free fixed dose combination of tafluprost 0.0015% and timolol 0.5% eye drops to ... | ||||||||||||||||||||||||||||
Medical condition: Patients diagnosed with ocular hypertension or open-angle glaucoma (primary open-angle glaucoma [POAG], capsular glaucoma or pigmentary glaucoma). | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: HU (Completed) LV (Completed) CZ (Completed) ES (Completed) PT (Completed) AT (Completed) BG (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-002235-25 | Sponsor Protocol Number: A1481131 | Start Date*: 2006-12-14 | |||||||||||
Sponsor Name:Pfizer Ltd, Ramsgate Rd, Sandwich, Kent, United Kingdom | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo Controlled, Dose Ranging, Parallel Group Study of Oral Sildenafil in the Treatment of Children, Aged 1-17 Years, With Pulmonary Arterial Hypertension | |||||||||||||
Medical condition: Pulmonary Arterial Hypertension | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FI (Prematurely Ended) SK (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004890-15 | Sponsor Protocol Number: EU-C-001-II-01 | Start Date*: 2019-06-05 | |||||||||||
Sponsor Name:Eustralis Pharmaceuticals Ltd. | |||||||||||||
Full Title: A double-blind placebo-controlled study with an open-label pilot phase, assessing the efficacy, tolerability and safety of EU-C-001 in patients with moderate to severe traumatic brain injury | |||||||||||||
Medical condition: Traumatic brain injury | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024512-34 | Sponsor Protocol Number: C-10-040 | Start Date*: 2011-05-17 | ||||||||||||||||
Sponsor Name:Alcon Research, Ltd. | ||||||||||||||||||
Full Title: Safety and IOP-Lowering Efficacy of Brinzolamide 10 mg/ml / Brimonidine 2 mg/ml Fixed Combination Eye Drops, Suspension compared to Brinzolamide 10 mg/ml Eye Drops, Suspension and Brimonidine 2 mg/... | ||||||||||||||||||
Medical condition: Open-angle glaucoma and ocular hypertension | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) PT (Completed) LV (Completed) DE (Completed) HU (Completed) LT (Completed) ES (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
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