- Trials with a EudraCT protocol (15)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
15 result(s) found for: Terlipressin.
Displaying page 1 of 1.
EudraCT Number: 2012-002275-33 | Sponsor Protocol Number: 0805-2012-1 | Start Date*: 2014-01-15 |
Sponsor Name:Dept. of Gastroenterology, Universityhospital Odense | ||
Full Title: Renal and cardiac effects of terlipressin and dobutamin in cirrhosis and ascites. A randomised study. | ||
Medical condition: Liver cirrhosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-004328-39 | Sponsor Protocol Number: INFUTER | Start Date*: 2020-04-13 |
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica_FCRB | ||
Full Title: Hemodynamic profile of terlipressin and octreotide in patients with cirrhosis and portal hypertension. A randomised, single blinded clinical trial. | ||
Medical condition: The proposed study aims to investigate the hemodynamic effects of terlipressin and the time profile of these effects in patients with cirrhosis and portal hypertension when given as continuous infu... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001199-31 | Sponsor Protocol Number: 57231 | Start Date*: 2017-03-20 |
Sponsor Name: | ||
Full Title: Improving treatment of right ventricular failure in pulmonary hypertension patients. | ||
Medical condition: End stage right ventricular failure in pulmonary hypertension patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-005756-37 | Sponsor Protocol Number: CONTENTSS | Start Date*: 2021-11-02 | ||||||||||||||||
Sponsor Name:Fundación Pública Andaluza para la Gestión de la | ||||||||||||||||||
Full Title: Double blind randomized clinical trial comparing noradrenaline plus placebo versus noradrenaline plus terlipressin in septic shock | ||||||||||||||||||
Medical condition: Patients with septic shock who remain without reaching the hemodynamic goal of TAM> 65 mmHg, despite volume replacement and administration of noradrenaline at doses equal to or greater than 0.2 μg ... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002837-19 | Sponsor Protocol Number: RD-5103-037-05 | Start Date*: 2007-04-16 | |||||||||||
Sponsor Name:DERBY HOSPITALS NHS FOUNDATION TRUST | |||||||||||||
Full Title: A DOUBLE BLIND PLACEBO CONTROLLED TRIAL OF TERLIPRESSIN IN THE MANAGEMENT OF SEVERE ALCOHOLIC HEPATITIS – A PRELIMINARY STUDY | |||||||||||||
Medical condition: Severe alcoholic hepatitis as judged by a Maddrey score >32 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-005182-37 | Sponsor Protocol Number: OT-0401 | Start Date*: 2005-07-25 | |||||||||||
Sponsor Name:Curatis Pharma GmbH | |||||||||||||
Full Title: A double-blind, randomized, placebo-controlled, multicenter phase III study of intravenous terlipressin in patients with hepatorenal syndrome type 1 | |||||||||||||
Medical condition: Hepatorenal Syndrome Type 1 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000513-12 | Sponsor Protocol Number: NR 9284-3 | Start Date*: 2007-02-15 | |||||||||||
Sponsor Name:Úrazová nemocnice brno | |||||||||||||
Full Title: Terlipressin in the treatment of catecholamine-resistant septic shock | |||||||||||||
Medical condition: Septic shock refractory to standard dose of norepinephrine | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005931-58 | Sponsor Protocol Number: APHP200043 | Start Date*: 2021-04-02 |
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | ||
Full Title: ACTIVE : ACid tranexamic or Terlipressin for Initial emergency treatment of mild to seVere hEmoptysis | ||
Medical condition: Hemoptysis, whatever the cause, with the exception of cystic fibrosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002166-20 | Sponsor Protocol Number: AMELIORATE | Start Date*: 2012-02-08 | ||||||||||||||||
Sponsor Name:Fundació Clinic per a la Recerca Biomèdica | ||||||||||||||||||
Full Title: Treatment of hepatorenal syndrome with terlipressin infusion adjusted to hemodynamic response | ||||||||||||||||||
Medical condition: Hepatorenal syndrome (HRS) type 1 | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005090-21 | Sponsor Protocol Number: NA-TER | Start Date*: 2006-10-26 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA S. GIOVANNI BATTISTA DI TORINO | |||||||||||||
Full Title: Noradrenalin vs terlipressin in patients with hepatorenal syndrome | |||||||||||||
Medical condition: Hepatorenal syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000236-26 | Sponsor Protocol Number: CRLX030X2201 | Start Date*: 2012-11-06 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: An exploratory study to investigate the haemodynamic effects of serelaxin in patients with compensated cirrhosis and portal hypertension | |||||||||||||
Medical condition: Compensated alcohol-related cirrhosis and portal hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024138-43 | Sponsor Protocol Number: AN-2010/28 | Start Date*: 2011-06-27 | |||||||||||
Sponsor Name:Javier Pascual Ramírez | |||||||||||||
Full Title: Protocolo de suero salino hipertónico y terlipresina en la mejora funcional del shock séptico | |||||||||||||
Medical condition: Shock séptico | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001420-34 | Sponsor Protocol Number: 0001 | Start Date*: 2020-04-14 | |||||||||||
Sponsor Name:Aarhus University | |||||||||||||
Full Title: Senicapoc in COVID-19 Patients with Severe Respiratory Insufficiency – A Randomized, Open-Label, Phase II Trial | |||||||||||||
Medical condition: Infection with COVID19 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003942-35 | Sponsor Protocol Number: APHP200018 | Start Date*: 2021-04-27 | |||||||||||
Sponsor Name:Assistance Publique - Hôpitaux Paris | |||||||||||||
Full Title: HydrOcortisone and fludRocortisoNe for critical ILLness-related corticosteroid insufficiency | |||||||||||||
Medical condition: Critically ill patients with a SOFA score (SOFA; Sequential Organ Failure Assessment) ≥ 6, for at least 6 consecutive hours, suffering from CIRCI, to the notable exception of patients with septic s... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001969-33 | Sponsor Protocol Number: TAK-242-2001 | Start Date*: 2020-05-28 | |||||||||||
Sponsor Name:Akaza Bioscience Limited | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Proof-of-Concept, Phase 2a Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Intravenous TAK-242 in Subj... | |||||||||||||
Medical condition: Acute Alcoholic Hepatitis Causing Decompensation of Alcohol related Cirrhosis and Acute-on-Chronic Liver Failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Prematurely Ended) HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
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