- Trials with a EudraCT protocol (29)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
29 result(s) found for: hydrocortisone sodium succinate.
Displaying page 1 of 2.
EudraCT Number: 2007-004822-26 | Sponsor Protocol Number: SFPT/01 | Start Date*: 2007-12-20 |
Sponsor Name:Birmingham Children's Hospital | ||
Full Title: A randomised pilot trial of a steroid-free immunosuppressant regimen in paediatric liver transplantation | ||
Medical condition: Post isolated liver transplant complications | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-000212-16 | Sponsor Protocol Number: HYKS-190116 | Start Date*: 2016-04-12 |
Sponsor Name:Helsinki University Central Hospital | ||
Full Title: Hydrocortisone vs. pasireotide in preventing pancreatic fistula and other complications after pancreatic resection - a prospective, randomized, controlled trial | ||
Medical condition: Patients undergoing pancreatic resection. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-001580-30 | Sponsor Protocol Number: 2006.SUR.ORT.01 | Start Date*: 2006-10-13 |
Sponsor Name:Royal Cornwall Hospitals NHS Trust | ||
Full Title: Investigation into the effects of steroid and local anaesthetic infiltration into soft tissues in total hip replacement wounds on post-operative pain relief. | ||
Medical condition: patients undergoing total hip replacement surgery for osteoarthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000182-45 | Sponsor Protocol Number: 2013AT001B | Start Date*: 2014-04-02 | |||||||||||
Sponsor Name:Royal Brompton and Harefield NHS Foundation Trust | |||||||||||||
Full Title: A pilot study into health pre and post treatment with intravenous Aminophylline and Hydrocortisone in severe asthmatics | |||||||||||||
Medical condition: Severe asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001395-15 | Sponsor Protocol Number: Awaiting | Start Date*: 2020-04-06 | ||||||||||||||||
Sponsor Name:Deparment of Intensive Care, Rigshospitalet | ||||||||||||||||||
Full Title: Low dose hydrocortisone in patients with COVID-19 and severe hypoxia – the COVID STEROID trial | ||||||||||||||||||
Medical condition: Adult patients with COVID-19 and severe hypoxia. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-019178-33 | Sponsor Protocol Number: BRD/10/1-L | Start Date*: 2010-05-27 | |||||||||||
Sponsor Name:CHU de Nantes | |||||||||||||
Full Title: Traitement de l'insuffisance surrénale secondaire à un traumatisme crânien grave. Etude multicentrique, contrôlée, randomisée portant sur un médicament. - Etude Corti-TC" | |||||||||||||
Medical condition: Insuffisance surrénale secondaire à un traumatisme crânien grave | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002346-30 | Sponsor Protocol Number: HC-SAP-012008 | Start Date*: 2008-10-03 | |||||||||||
Sponsor Name:Esko Kemppainen | |||||||||||||
Full Title: SUPRAFYSIOLOGINEN HYDROKORTISONI VAIKEASSA AKUUTISSA HAIMATULEHDUKSESSA | |||||||||||||
Medical condition: Vaikea akuutti haimatulehdus, johon liittyy verenkiertovajaus | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024273-38 | Sponsor Protocol Number: UZ1 | Start Date*: 2013-11-27 |
Sponsor Name:University Hospitals Leuven | ||
Full Title: Supplemental corticosteroids in cirrhotic hypotensive patients with suspicion of sepsis | ||
Medical condition: Cirrhotic patients under vasopressors admitted to the ICU because of persisting hypotension and with suspected infection. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Prematurely Ended) CZ (Completed) GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2014-005186-73 | Sponsor Protocol Number: WADA2014Pred | Start Date*: 2015-03-18 |
Sponsor Name:Bispebjerg University Hospital | ||
Full Title: Impact of intense exercise on pharmacokinetics of glucocorticoides in relation to doping analysis | ||
Medical condition: Impact of intense exercise on pharmacokinetics of glucocorticoids in relation to doping analysis | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003158-10 | Sponsor Protocol Number: GI-CCT372273 | Start Date*: 2014-04-11 | |||||||||||
Sponsor Name:The George Institute for Global Health | |||||||||||||
Full Title: ADRENAL- ADjunctive coRticosteroid trEatment iN criticAlly ilL patients with septic shock. | |||||||||||||
Medical condition: Septic Shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DK (Completed) IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001795-38 | Sponsor Protocol Number: ALLTogether1 | Start Date*: 2020-05-15 | |||||||||||
Sponsor Name:Karolinska University Hospital | |||||||||||||
Full Title: ALLTogether1– A Treatment study protocol of the ALLTogether Consortium for children and young adults (0-45 years of age) with newly diagnosed acute lymphoblastic leukaemia (ALL) | |||||||||||||
Medical condition: Acute lymphoblastic leukaemia (ALL) | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) FI (Trial now transitioned) SE (Trial now transitioned) DK (Trial now transitioned) IE (Trial now transitioned) GB (GB - no longer in EU/EEA) BE (Trial now transitioned) PT (Trial now transitioned) LT (Trial now transitioned) NO (Trial now transitioned) NL (Trial now transitioned) FR (Trial now transitioned) IS (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001620-33 | Sponsor Protocol Number: APHP200033 | Start Date*: 2021-01-13 |
Sponsor Name:ASSISTANCE-PUBLIQUE HOPITAUX DE PARIS (AP-HP) | ||
Full Title: HYdrocortisone and VAsopressin in Post-RESuscitation Syndrome | ||
Medical condition: Adult cardiac arrest patients with sustained ROSC and hemodynamic failure due to post-resuscitation syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005822-23 | Sponsor Protocol Number: REK231814 | Start Date*: 2012-10-16 | |||||||||||
Sponsor Name:Haukeland University Hospital | |||||||||||||
Full Title: CONTINUOUS SUBCUTANEOUS HYDROCORTISONE INFUSION IN CONGENITAL ADRENAL HYPERPLASIA | |||||||||||||
Medical condition: Congenital adrenal hyperplasia (CAH) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) SE (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2010-022640-20 | Sponsor Protocol Number: JL23 | Start Date*: 2011-01-12 | |||||||||||
Sponsor Name:Johanna Laukkarinen | |||||||||||||
Full Title: Cortisone treatment for the prevention of postoperative pancreatitis and pancreatitis-induced complications after pancreaticoduodenectomy (Whipple operation). | |||||||||||||
Medical condition: Tutkittavat potilaat ovat leikkauspotilaita, joille suoritetaan rutiinisti haimanpään-ja pohjukaissuolen poistoleikkaus (Whipplen operaatio) joko kasvaimen tai kroonisen haimatulehduksen vuoksi. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003097-97 | Sponsor Protocol Number: 00029 | Start Date*: 2009-03-09 | |||||||||||
Sponsor Name:HUS | |||||||||||||
Full Title: Endoskooppinen kortisoni vaikean juveniilin parotiitin hoidossa | |||||||||||||
Medical condition: juveniili parotiitti | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002788-28 | Sponsor Protocol Number: RHM CHI434 | Start Date*: 2008-01-15 | ||||||||||||||||
Sponsor Name:Southampton University Hospital NHS Trust | ||||||||||||||||||
Full Title: Evaluation of Corticosteroid therapy in Childhood Severe Sepsis (Steroids in Paediatric Sepsis, StePS) - a randomised pilot study | ||||||||||||||||||
Medical condition: Children with severe sepsis requiring mechanical ventilation presenting within 12 hours of onset. The majority of children will either have community acquired sepsis (most commonly meningococcal or... | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004401-10 | Sponsor Protocol Number: HYPRESS | Start Date*: 2008-01-15 | |||||||||||
Sponsor Name:Charité Universitätsmedizin Berlin | |||||||||||||
Full Title: Hydrocortisone for Prevention of Septic Shock Placebo-controlled, randomised, double-blind study to investigate the efficacy and safety of low dose hydrocortisone to prevent the development of se... | |||||||||||||
Medical condition: Patients with severe sepsis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010917-61 | Sponsor Protocol Number: NSDnr.17525 | Start Date*: 2010-08-25 | |||||||||||
Sponsor Name:Haukeland University hospital | |||||||||||||
Full Title: Glucocorticoid Replacement in Addison's disease | |||||||||||||
Medical condition: Autoimmune Addison's disease is a rare and chronic disease wich leads to primary adrenal failure. The conventional glucocorticoid replacement therapy in primary adrenal insufficiency (Addison’s dis... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017066-23 | Sponsor Protocol Number: RituxiRT | Start Date*: 2010-01-25 | |||||||||||
Sponsor Name:Guys and St Thomas Foundation Trust | |||||||||||||
Full Title: A randomized trial of Rituximab in induction therapy for living donor renal transplantation | |||||||||||||
Medical condition: End stage renal disease; renal function after renal transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
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