- Trials with a EudraCT protocol (158)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
158 result(s) found for: Complications of hypertension.
Displaying page 1 of 8.
EudraCT Number: 2013-003144-23 | Sponsor Protocol Number: PANDA | Start Date*: 2014-02-03 | |||||||||||||||||||||
Sponsor Name:King's College London [...] | |||||||||||||||||||||||
Full Title: Pregnancy And chronic hypertension: NifeDipine or labetalol as Antihypertensive treatment | |||||||||||||||||||||||
Medical condition: Chronic hypertension in pregnancy | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-003778-29 | Sponsor Protocol Number: CTU/2013/064 | Start Date*: 2014-01-30 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: Combined Multi-Marker Screening and Randomised Patient Treatment with Aspirin for Evidence-based Pre-eclampsia Prevention | |||||||||||||
Medical condition: Pre-eclampsia | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) IT (Completed) BE (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000419-34 | Sponsor Protocol Number: RC15_0475 | Start Date*: 2016-10-24 | |||||||||||
Sponsor Name:CHU de Nantes | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023241-29 | Sponsor Protocol Number: 747-204 | Start Date*: 2011-02-10 | |||||||||||
Sponsor Name:Intercept Pharmaceuticals Inc | |||||||||||||
Full Title: A Pilot Study to Evaluate the Safety, Tolerability and Efficacy of Obeticholic Acid (INT-747) for the Treatment of Portal Hypertension (PESTO) | |||||||||||||
Medical condition: Portal Hypertension in Patients with Cirrhosis | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024175-58 | Sponsor Protocol Number: kardioIKEM2010 | Start Date*: 2011-06-30 | ||||||||||||||||
Sponsor Name:IKEM | ||||||||||||||||||
Full Title: Comparison of two treatment options for hypertension in heart transplant recipients | ||||||||||||||||||
Medical condition: Compensation of arterial hypertension in heart transplant recipients. Renal function and its changes in heart transplant recipients. | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004559-12 | Sponsor Protocol Number: SPP635CRD05 | Start Date*: 2007-11-07 | ||||||||||||||||||||||||||
Sponsor Name:Speedel Pharma Ltd. | ||||||||||||||||||||||||||||
Full Title: A Phase II a, Double-Blind, Randomized, Parallel-Design, Four-week Study to Investigate the Efficacy and Safety of Two Different Doses of the Renin-inhibitor SPP635 Once Daily in Type II Diabetic P... | ||||||||||||||||||||||||||||
Medical condition: Diabetes mellitus type II with mild to moderate hypertension and albuminuria | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IE (Completed) HU (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-005523-27 | Sponsor Protocol Number: CIRROXABAN | Start Date*: 2015-07-30 |
Sponsor Name:INSTITUTO DE INVESTIGACIONES BIOMEDICAS AUGUST PI I SUNYER (IDIBAPS) | ||
Full Title: Multicenter prospective randomized trial of the effect of rivaroxaban on survival and development of complications of portal hypertension in patients with cirrhosis | ||
Medical condition: Liver cirrhosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
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 | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: | Gender: Female | ||||||||||||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005130-22 | Sponsor Protocol Number: FFIS/2015/01/ST | Start Date*: 2016-08-03 | |||||||||||
Sponsor Name:Fundación para la Formación e Investigación Sanitaria (FFIS) | |||||||||||||
Full Title: Randomised Controlled Trial with Pravastatin versus Placebo for Prevention of Pre-eclampsia | |||||||||||||
Medical condition: Pre-eclampsia | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Prematurely Ended) BE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-005206-19 | Sponsor Protocol Number: FFIS/2016/02/ST | Start Date*: 2017-05-26 | |||||||||||
Sponsor Name:Fundación para la Formación e Investigación Sanitaria (FFIS) | |||||||||||||
Full Title: Randomised Controlled Trial with Pravastatin versus Placebo for Prevention of Preeclampsia | |||||||||||||
Medical condition: Pre-eclampsia | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) ES (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000036-96 | Sponsor Protocol Number: CR0014 | Start Date*: 2018-09-06 | |||||||||||
Sponsor Name:Ablative Solutions, Inc. | |||||||||||||
Full Title: A Phase 2, Multicenter, Blinded, Sham Procedure-Controlled Trial of Renal Denervation by the Peregrine System Kit, in Subjects with Hypertension, in the Absence of Antihypertensive Medications | |||||||||||||
Medical condition: Hypertension | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (GB - no longer in EU/EEA) DE (Completed) IE (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005330-10 | Sponsor Protocol Number: 987654321 | Start Date*: 2013-03-14 |
Sponsor Name:Erasmus University Medical Centre | ||
Full Title: Maternal pharmacokinetics and pharmacodynamics of nicardipine (iv) during treatment of severe hypertension in pregnancy. | ||
Medical condition: Pregnant patients with preeclampsia (hypertension and protein/creatinine ratio ≥ 30mg/mmol or ≥ 300mg protein/24hours) complicated with severe hypertension (systolic bloodpressure ≥ 160mmHg and/or ... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-005811-34 | Sponsor Protocol Number: 24d005 | Start Date*: 2018-07-05 |
Sponsor Name:VU Medical Center, Amsterdam | ||
Full Title: Pregnancy reLated Acute hyperTension INtervention Action: a randomized trial comparing labetalol and nicardipine in women with acute hypertension in pregnancy (Platina-trial) | ||
Medical condition: To asses optimal treatment of hypertension of hypertensive disorders in pregnancy | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004160-58 | Sponsor Protocol Number: CHASAP | Start Date*: 2021-06-11 | ||||||||||||||||
Sponsor Name:Centre hospitalier intercommunal de Créteil | ||||||||||||||||||
Full Title: Chronic Hypertension and Acetyl Salicylic Acid in Pregnancy, a multicenter prospective randomized double-blind placebo-controlled trial | ||||||||||||||||||
Medical condition: Pregnant women with chronic hypertension | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002587-24 | Sponsor Protocol Number: CMD_ALISKIREN | Start Date*: 2011-10-20 | |||||||||||
Sponsor Name:FONDAZIONE CENTRO S. RAFFAELE DEL MONTE TABOR | |||||||||||||
Full Title: Effects of Aliskiren on microcirculation dysfunction in patients affected by hypertension | |||||||||||||
Medical condition: dysfunction of coronary microcirculation in arterial hypertension | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004473-32 | Sponsor Protocol Number: IDN-6556-14 | Start Date*: 2016-12-27 | ||||||||||||||||
Sponsor Name:Conatus Pharmaceuticals Inc. | ||||||||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial of Emricasan, an Oral Caspase Inhibitor, in Subjects with Non-alcoholic Steatohepatitis (NASH) Cirrhosis and Severe Portal Hyperten... | ||||||||||||||||||
Medical condition: Non-Alcoholic Steatohepatitis (NASH) Cirrhosis and Severe Portal Hypertension | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) ES (Completed) FR (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 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000811-26 | Sponsor Protocol Number: STOPPRE | Start Date*: 2018-09-19 | |||||||||||
Sponsor Name:Vall D'Hebron Institut de Recerca (VHIR) | |||||||||||||
Full Title: A phase III, multicentric, Randomized, open-label, parallel-group clinical trial to detect false positives from first-trimester preeclampsia screening (StopPRE) at the second-trimester of pregnancy. | |||||||||||||
Medical condition: First-trimester pre-eclampsia patients | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001918-42 | Sponsor Protocol Number: 2009-107(Canadian) | Start Date*: 2014-01-17 | |||||||||||
Sponsor Name:Ottawa Hospital Research Institute | |||||||||||||
Full Title: Effect of folic acid supplementation in pregnancy on preeclampsia - Folic Acid Clinical Trial (FACT) A randomized, double-blind, placebo-controlled, Phase III, international multi-centre study of 4... | |||||||||||||
Medical condition: pre-eclampsia | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002545-32 | Sponsor Protocol Number: CR0002 | Start Date*: 2019-11-06 | |||||||||||
Sponsor Name:Ablative Solutions, Inc | |||||||||||||
Full Title: A Pivotal, Multicenter, Blinded, Sham Procedure-Controlled Trial of Renal Denervation by the Peregrine System™ Kit, in Subjects with Hypertension. | |||||||||||||
Medical condition: Hypertension | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Trial now transitioned) SE (Ongoing) BE (Trial now transitioned) NL (Trial now transitioned) IE (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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

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. |
