- Trials with a EudraCT protocol (80)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
80 result(s) found for: Adrenal insufficiency.
Displaying page 1 of 4.
EudraCT Number: 2021-002528-18 | Sponsor Protocol Number: RESCUE2131PE9 | Start Date*: 2022-02-22 | |||||||||||
Sponsor Name:Copenhagen University Hospital Rigshospitalet | |||||||||||||
Full Title: RESCUE - Effect of supplemental hydrocortisone during stress in prednisolone-induced adrenal insufficiency; A multicentre, randomised, double blinded, placebo-controlled clinical trial on health-re... | |||||||||||||
Medical condition: Glucocorticoid-induced adrenal insufficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-006121-65 | Sponsor Protocol Number: 65411807 | Start Date*: 2021-08-31 | |||||||||||
Sponsor Name:Odense University Hospital | |||||||||||||
Full Title: STUDY PROTOCOL: A multi-centre, randomized, double-blinded, placebo controlled 1-year study to compare the effect of hydrocortisone and palcebo in patients with partial adrenal insufficiency after ... | |||||||||||||
Medical condition: To investigate the effects of hydrocortisone replacement in participants with previous PMR and GCA, who are in GC-free remission and exhibit biochemical evidence of mild to moderate adrenal insuffi... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003241-15 | Sponsor Protocol Number: SCH/12/043 | Start Date*: 2012-10-09 | ||||||||||||||||
Sponsor Name:Sheffield Children's NHS Foundation Trust | ||||||||||||||||||
Full Title: NeSST2: A multi-stage clinical study to develop a non-invasive Short Synacthen Test (SST) with nasally administered Synacthen and salivary cortisol. The validated non-invasive SST will be used to e... | ||||||||||||||||||
Medical condition: In stages 1+2 of the study healthy volunteers will be used to determine the bioequivalence of nasal Synacthen with 1 microgram of intravenous synacthen. Stage 3 will use healthy children to establi... | ||||||||||||||||||
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Population Age: Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004772-21 | Sponsor Protocol Number: Dual_Hydrocortisone_gluc_variabilit | Start Date*: 2018-02-22 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA INTEGRATA VERONA | |||||||||||||
Full Title: Dual-release hydrocortisone compared to immediate-release glucocorticoid replacement therapy in terms of glucose control, insulin sensitivity and glucose variability in patients with adrenal insuff... | |||||||||||||
Medical condition: adrenal insufficienty | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001682-33 | Sponsor Protocol Number: 6176/RADS2 | Start Date*: 2012-09-06 | |||||||||||||||||||||
Sponsor Name:Newcastle upon Tyne Hospitals NHS Foundation Trust | |||||||||||||||||||||||
Full Title: Combined Immunotherapy and Trophic Adrenocortical Stimulation in New Onset Autoimmune Addison’s Disease | |||||||||||||||||||||||
Medical condition: Autoimmune Addison's disease: autoimmune primary adrenal insufficiency | |||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-013355-29 | Sponsor Protocol Number: SCH/09/018 | Start Date*: 2010-07-02 | ||||||||||||||||
Sponsor Name:Sheffield Children's NHS Foundation Hospital | ||||||||||||||||||
Full Title: A multi-stage clinical study to develop a non-invasive Short Synacthen Test (SST) with nasally administered synacthen and salivary cortisol. The validated non-invasive SST will be used to establish... | ||||||||||||||||||
Medical condition: In stages 1+2 of the study healthy volunteers will be used to determine the bioequivalence of nasal synacthen with 1 microgram of intravenous synacthen. Stage 3 will use healthy children to establi... | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-018209-32 | Sponsor Protocol Number: DHEA091209 | Start Date*: 2010-02-17 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA "S. GIOVANNI BATTISTA DI TORINO" | |||||||||||||
Full Title: EFFECTS OF DHEA TREATMENT ON ANTHROPOMETRIC AND METABOLIC PARAMETERS, AND ON QUALITY OF LIFE (QOL) IN PATIENTS WITH ADDISON S DISEASE UNDER GLUCORTICOID-MINERALCORTICOID SUBSTITUTIVE TREATMENT | |||||||||||||
Medical condition: Addison s disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000260-28 | Sponsor Protocol Number: Infacort001 | Start Date*: 2013-06-26 | |||||||||||
Sponsor Name:Diurnal Ltd | |||||||||||||
Full Title: A single centre, open label, randomised, crossover study in dexamethasone-suppressed healthy adult male volunteers to compare the pharmacokinetics of Infacort® versus immediate-release hydrocortiso... | |||||||||||||
Medical condition: Adrenal Insufficiency | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002336-15 | Sponsor Protocol Number: 578 | Start Date*: 2011-08-31 | ||||||||||||||||
Sponsor Name:King's College London [...] | ||||||||||||||||||
Full Title: The effect of prednisolone versus hydrocortisone as glucocorticoid replacement therapy on hypoglycaemia frequency in people with Type 1 diabetes and adrenal insufficiency: a pilot study. | ||||||||||||||||||
Medical condition: Type 1 diabetes and adrenal insufficiency. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-000056-14 | Sponsor Protocol Number: 06/DTD/3791E | Start Date*: 2008-03-03 | ||||||||||||||||
Sponsor Name:Cardiff University | ||||||||||||||||||
Full Title: Determination of method-specific normal cortisol and adrenal hormone responses to the short Synacthen test | ||||||||||||||||||
Medical condition: Normal, healthy volunteers to establish a reference range for the synacthen test, plus patients with hypoadrenalism/hypopituitarism | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-003990-42 | Sponsor Protocol Number: DC08/01 | Start Date*: 2008-07-28 | |||||||||||
Sponsor Name:DuoCort Pharma AB | |||||||||||||
Full Title: An open, multi-centre, phase IIIb, long term follow-up study to assess the safety, tolerability and efficacy of once-daily oral modified-release hydrocortisone in patients with adrenal insufficiency. | |||||||||||||
Medical condition: Primary adrenal insufficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2009-018074-56 | Sponsor Protocol Number: G0900001:RoSAv1.1:12_09 | Start Date*: 2010-05-05 | |||||||||||
Sponsor Name:Newcastle upon Tyne Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Revival of autochthonous adrenocortical stem cells in autoimmune Addison’s disease (RoSA) | |||||||||||||
Medical condition: Autoimmune Addison's disease | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004028-12 | Sponsor Protocol Number: PLEN2013 | Start Date*: 2014-05-13 | |||||||||||
Sponsor Name:Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico | |||||||||||||
Full Title: Replacement therapy with modified-release hydrocortisone (Plenadren) in patients with central adrenal insufficiency | |||||||||||||
Medical condition: Central hypoadrenalism | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-007084-89 | Sponsor Protocol Number: DC 06/02 | Start Date*: 2007-04-20 | |||||||||||
Sponsor Name:DuoCort Pharma AB | |||||||||||||
Full Title: A randomised, controlled, open, two-armed, two-period cross-over, multi-centre phase II/III study to assess the safety, tolerability and pharmacokinetics of once-daily oral modified-release hydroco... | |||||||||||||
Medical condition: Primary adrenal insufficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002687-25 | Sponsor Protocol Number: PHYSCA-1 | Start Date*: 2011-11-16 | ||||||||||||||||
Sponsor Name:University Hospital of Wuerzburg | ||||||||||||||||||
Full Title: Pharmacokinetics of Hydrocortisone after Subcutaneous Administration Compared with Intramuscular Injection in Chronic Adrenal Insufficiency (PHYSCA-Trial) | ||||||||||||||||||
Medical condition: Adrenal insufficiency under chronic glucocorticoid replacement | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-003062-18 | Sponsor Protocol Number: 4071 | Start Date*: 2008-06-05 | |||||||||||
Sponsor Name:Newcastle upon Tyne Hospitals NHS Trust | |||||||||||||
Full Title: Immunotherapeutic Rescue of steroidogenic function in autoimmune Addison’s Disease (RAD): Pilot study | |||||||||||||
Medical condition: Autoimmune Addison's disease (adrenocortical failure) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (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: 2005-000115-10 | Sponsor Protocol Number: SPON CU 086 | Start Date*: 2005-10-14 |
Sponsor Name:Cardiff University | ||
Full Title: A randomised, double blind, placebo-controlled, cross-over study of the effects of dehydroepiandrosterone replacement on vascular function in patients with primary and secondary adrenal insufficiency. | ||
Medical condition: Primary and secondary adrenal failure | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-006487-24 | Sponsor Protocol Number: ADNorGC | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Helse Bergen HF | |||||||||||||
Full Title: A registry-based, open-label, randomized study to investigate quality-of-life with Plenadren compared with Cortison in participants aged 16-80 with newly diagnosed primary adrenal insufficiency | |||||||||||||
Medical condition: Primary adrenal insufficiency | |||||||||||||
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Population Age: Adolescents, Under 18, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005170-30 | Sponsor Protocol Number: 07-031 | Start Date*: 2007-12-08 | |||||||||||
Sponsor Name:CHU CAEN | |||||||||||||
Full Title: Pharmacocinétique de l’Hydrocortisone chez le patient ADdisonien : évaluation de la valeur prédictive de l’ACTH plasmatique pour la titration du traitement substitutif | |||||||||||||
Medical condition: ADDISON'S DISEASE | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
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