- Trials with a EudraCT protocol (10)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
10 result(s) found for: Coversyl (perindopril).
Displaying page 1 of 1.
EudraCT Number: 2009-010058-37 | Sponsor Protocol Number: 1 | Start Date*: 2009-04-23 |
Sponsor Name:Odense University Hospital | ||
Full Title: Chronic subdural hematome - reduction of risc of recurrence by treatment with ACE inhibitors (in Danish: Kronisk subduralt hæmatom – reduktion af recidiv risiko ved behandling med ACE hæmmere) | ||
Medical condition: The project aims at investigating if treatment with the ACE inhibitor Coversyl (perindopril) for 3 months after surgery for chronic subdural hematom will decrease the risc of recurrence. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-003328-11 | Sponsor Protocol Number: DM4-90652-001 | Start Date*: 2012-11-14 | |||||||||||
Sponsor Name:Servier International / Les Laboratoires Servier | |||||||||||||
Full Title: | |||||||||||||
Medical condition: Arterial Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000749-13 | Sponsor Protocol Number: SPON CU 101 | Start Date*: 2005-07-30 |
Sponsor Name:Cardiff University | ||
Full Title: A Randomised Double-Blind Trial of Medical Treatment In Marfan Syndrome. | ||
Medical condition: Marfan Syndrome | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-004891-16 | Sponsor Protocol Number: CL3-05179-002 | Start Date*: 2021-10-20 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Evaluation of the clinical efficacy and safety of perindopril 10 mg/indapamide 2.5 mg/amlodipine 5 or 10 mg/bisoprolol 5 mg in single-pill combination after 8 weeks of treatment versus the free com... | |||||||||||||
Medical condition: Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) PT (Completed) LT (Completed) IT (Completed) LV (Completed) SK (Completed) HU (Completed) CZ (Completed) BG (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007026-22 | Sponsor Protocol Number: CL2-09490-157 | Start Date*: 2008-03-28 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Assessment of the effects on 24-hour ambulatory blood pressure and the safety of a once-a-day oral 8 mg perindopril morning administration versus evening administration in hypertensive patients. An... | |||||||||||||
Medical condition: Essential arterial hyperpertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020226-17 | Sponsor Protocol Number: CRO 1644 | Start Date*: 2010-12-23 | |||||||||||
Sponsor Name:Imperial College | |||||||||||||
Full Title: An evaluation of the effect of an angiotensin-converting enzyme (ACE) inhibitor on the growth rate of small abdominal aortic aneurysms | |||||||||||||
Medical condition: Abdominal Aortic Aneurysms | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003568-20 | Sponsor Protocol Number: RGR | Start Date*: 2008-08-08 |
Sponsor Name:Prof Alice Stanton | ||
Full Title: Renin Genotype and Response to Renin Angiotensin System Blockade. | ||
Medical condition: Hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-023184-18 | Sponsor Protocol Number: C10-44 | Start Date*: 2012-01-25 | |||||||||||
Sponsor Name:Inserm | |||||||||||||
Full Title: PRE clinical mutation CARriers from families with DIlated cardiomyopathy and ACE inhibitors (PRECARDIA-INHERITANCE study) Preventive effect of ACE inhibitor (perindopril) on the onset or progres... | |||||||||||||
Medical condition: dilated cardiomyopathy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002877-71 | Sponsor Protocol Number: 261409 | Start Date*: 2018-02-28 |
Sponsor Name:European Commission FP7 Health 2010 | ||
Full Title: cGMP Enhancing Therapeutic Strategy for HFpEF: The cGETS Study An interventional, single blind, multicentre study. | ||
Medical condition: HFpEF patients over 18 years old and concomitant arterial hypertension, overweight or obesity and pulmonary hypertension. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005886-21 | Sponsor Protocol Number: CL2-16257-073 | Start Date*: 2007-03-14 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Evaluation des effets de l’ivabradine 5 mg et 7.5 mg en 2 prises par jour par voie orale chez des patients insuffisants cardiaques avec une hypertension artérielle insuffisamment équilibrée par Per... | |||||||||||||
Medical condition: Insuffisance cardiaque | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
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