- Trials with a EudraCT protocol (3,586)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (30)
3,586 result(s) found for: Blood pressure.
Displaying page 1 of 180.
| EudraCT Number: 2008-005426-37 | Sponsor Protocol Number: 4733 | Start Date*: 2008-11-25 | ||||||||||||||||
| Sponsor Name:University Medical Center Utrecht | ||||||||||||||||||
| Full Title: The effect of sevoflurane and isoflurane on vasopressor need | ||||||||||||||||||
| Medical condition: Aim of this study is to determine the effect of isoflurane versus sevoflurane on blood pressure and systemic vascular resistance. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2009-017033-22 | Sponsor Protocol Number: 24052 | Start Date*: 2010-02-12 | |||||||||||
| Sponsor Name:Odense University Hospital | |||||||||||||
| Full Title: Syd Dansk Hypertensions- og Diabetes Studie Et prospektivt, dobbeltblindet, randomiseret multicenterstudie af effekten af spironolakton på blodtrykket hos type 2 diabetikere med behandlingsresiste... | |||||||||||||
| Medical condition: At undersøge i et randomiseret, placebokontrolleret, dobbeltblindet interventionsforsøg, om tillæg af spironolakton til anden antihypertensiv behandling af behandlingsresistente hypertonikere med t... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-024448-13 | Sponsor Protocol Number: 010884 | Start Date*: 2011-02-18 | |||||||||||
| Sponsor Name:Netherlands Heart Foundation | |||||||||||||
| Full Title: Effects of low-dose aspirin taken at bedtime on blood pressure of subjects with who use aspirin for prevention of recurrent cardiovascular events: the Aspirin In Reduction of Tension II (ASPIRETENS... | |||||||||||||
| Medical condition: The medical condition to be investigated is hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-023988-17 | Sponsor Protocol Number: 260777 | Start Date*: 2014-04-04 | |||||||||||
| Sponsor Name:BrepCo Biopharma Limited | |||||||||||||
| Full Title: Management of Hypotension In the Preterm: A multi centre, randomised, controlled trial of hypotension management in the extremely low gestational age newborn | |||||||||||||
| Medical condition: Low Blood Pressure | |||||||||||||
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| Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Prematurely Ended) CZ (Prematurely Ended) BE (Prematurely Ended) GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-000165-23 | Sponsor Protocol Number: INFORM | Start Date*: 2016-10-19 | |||||||||||
| Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and University of Cambridge | |||||||||||||
| Full Title: ComparIsoN oF Optimal Hypertension RegiMens (Part of the Ancestry Informative Markers in Hypertension (AIM HY) Programme – AIM HY-INFORM) | |||||||||||||
| Medical condition: Cardiovascular Hemodynamics | |||||||||||||
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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: 2005-000333-38 | Sponsor Protocol Number: Hcy2005 | Start Date*: 2005-05-25 |
| Sponsor Name:Organisation name was not entered | ||
| Full Title: A randomized placebo-controlled trial to investigate blood pressure lowering effects of folic acid in patients with borderline hypertension. | ||
| Medical condition: Patients with hyperhomocysteinemia and high-normal blood pressure, otherwise healthy | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-004190-16 | Sponsor Protocol Number: 69HCL14-0248 | Start Date*: 2014-12-02 | |||||||||||
| Sponsor Name:Hospices Civils de Lyon | |||||||||||||
| Full Title: Determination of the optimal dose of ephedrine to treat hypotension during surgery of newborn to six months infant | |||||||||||||
| Medical condition: Arterial Hypotension | |||||||||||||
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| Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-001580-12 | Sponsor Protocol Number: GIRARD-WOLFF-2014 | Start Date*: 2014-12-19 | |||||||||||
| Sponsor Name:CHU de DIJON | |||||||||||||
| Full Title: | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: FR (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003204-40 | Sponsor Protocol Number: PATHBP_2013 | Start Date*: 2014-01-20 | ||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:University of Edinburgh [...] | ||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Paracetamol treatment in hypertension: effect on blood pressure | ||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Hypertension | ||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2015-003049-24 | Sponsor Protocol Number: PHY201501 | Start Date*: 2016-07-27 |
| Sponsor Name:Uppsala University, Department of Medical Sciences | ||
| Full Title: The Precision Hypertension Care study | ||
| Medical condition: Hypertension | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-002513-12 | Sponsor Protocol Number: 6084 | Start Date*: 2007-02-06 | |||||||||||
| Sponsor Name:Sangart, Inc. | |||||||||||||
| Full Title: A multi-center, randomized, double-blind, controlled Phase III study of the efficacy and safety of an oxygen-carrying colloid and plasma expander, Hemospan, compared with colloid (Voluven) for prev... | |||||||||||||
| Medical condition: Prevention of hypotensive episodes during anesthesia/surgery and through the postoperative period (defined as the first 6 hours following skin closure) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) BE (Completed) SE (Completed) GB (Completed) NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-002514-35 | Sponsor Protocol Number: 6090 | Start Date*: 2007-01-04 | |||||||||||
| Sponsor Name:Sangart, Inc. | |||||||||||||
| Full Title: A multi-center, randomized, double-blind, controlled Phase III study of the efficacy and safety of an oxygen-carrying colloid and plasma expander, Hemospan, compared with colloid (Voluven) for trea... | |||||||||||||
| Medical condition: Treatment of perioperative hypotension in patients undergoing primary hip arthroplasty with spinal anesthesia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) CZ (Completed) BE (Completed) SE (Completed) GB (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-001283-10 | Sponsor Protocol Number: NL80929.091.22 | Start Date*: 2022-06-28 |
| Sponsor Name:Radboud University Medical Center | ||
| Full Title: The effects of medication induced blood pressure reduction on cerebral hemodynamics in hypertensive frail elderly | ||
| Medical condition: Hypertension | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-021987-13 | Sponsor Protocol Number: NL29900.04 | Start Date*: 2010-10-15 | |||||||||||
| Sponsor Name:University Medical Center Groningen | |||||||||||||
| Full Title: Renal Hemodynamic Effects of ALiskiren (rasilez) in comparison to ramipril (Tritrace) in patients with overweigHt/obeSiTy and UntreateD hYpertension: The renal HEALTH-STUDY | |||||||||||||
| Medical condition: Glomerular hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-003567-31 | Sponsor Protocol Number: KPUK0106 | Start Date*: 2007-05-25 | ||||||||||||||||
| Sponsor Name:Med. Klinik II, Grosshadern, Klinikum der Universität München | ||||||||||||||||||
| Full Title: Regulation of Inflammatory Parameters by Telmisartan in Hypertensive Patients | ||||||||||||||||||
| Medical condition: hypertension metabolic syndrome | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Ongoing) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-000509-54 | Sponsor Protocol Number: MB121-008 | Start Date*: 2012-09-12 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Phase 2B Trial to Evaluate the Safety and Efficacy of BMS-823778 in Overweight and Obese Subjects with Inadequately Cont... | |||||||||||||
| Medical condition: Hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-003407-17 | Sponsor Protocol Number: CLD-1-2021 | Start Date*: 2022-04-19 | |||||||||||
| Sponsor Name:University Clinic of Nephrology and Hypertension | |||||||||||||
| Full Title: Combined effects of potassium, nitrate and sodium on blood pressure in patients with hypertension | |||||||||||||
| Medical condition: Essential Hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-000869-38 | Sponsor Protocol Number: VGSKAS-12916 | Start Date*: 2008-06-02 |
| Sponsor Name:Skaraborg Hospital | ||
| Full Title: Impact of Losartan in hypertensive men with obstructive sleep apnea | ||
| Medical condition: Hypertension and obstructive sleep apnea (OSA) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-005327-27 | Sponsor Protocol Number: KOR15.1 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Robugen GmbH [...] | ||
| Full Title: Effects of Korodin Herz-Kreislauf-Tropfen on low blood pressure and cognitive functions in adolescents | ||
| Medical condition: low blood pressure | ||
| Disease: | ||
| Population Age: Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-003843-28 | Sponsor Protocol Number: STH13565 | Start Date*: 2005-03-18 |
| Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | ||
| Full Title: The acute effects of testosterone administration in patients with pulmonary hypertension | ||
| Medical condition: Pulmonary Hypertension | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
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