- Trials with a EudraCT protocol (99)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
99 result(s) found for: Family support.
Displaying page 1 of 5.
EudraCT Number: 2012-002107-17 | Sponsor Protocol Number: RG_11-152 | Start Date*: 2013-02-01 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: International Randomised Controlled Trial for the Treatment of Newly Diagnosed Ewing's Sarcoma Family of Tumours | |||||||||||||
Medical condition: Ewing's Sarcoma Family of Tumours | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Ongoing) BE (Completed) CZ (Completed) IE (Completed) HU (Completed) NL (Completed) DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004177-83 | Sponsor Protocol Number: 37202 | Start Date*: 2011-11-14 | |||||||||||
Sponsor Name:Academic Medical Center | |||||||||||||
Full Title: Boosting the oxytocin system in acute trauma: The effectiveness of intranasal oxytocin treatments and stimulation of social support on preventing trauma related psychopathology | |||||||||||||
Medical condition: Posttraumatic Stress Disorder (PTSD) according to criteria in the DSM-IV | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000492-16 | Sponsor Protocol Number: CCR2739 | Start Date*: 2006-07-20 | |||||||||||
Sponsor Name:Royal Marsden Foundation Hospital | |||||||||||||
Full Title: A Phase II, Single-Centre, Randomised, Controlled, Open-Label Clinical Trial to Compare the Efficacy and Safety of Three Therapeutic Interventions on the Treatment of Hypothalamic Obesity due to Ch... | |||||||||||||
Medical condition: Hypothalamic Obesity due to Childhood Cancer with Cranial Insults | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001722-66 | Sponsor Protocol Number: REP_COVID | Start Date*: 2020-04-23 | ||||||||||||||||
Sponsor Name:Fundació Clínic per a la recerca Biomèdica | ||||||||||||||||||
Full Title: Plasma turnover in patients with COVID-19 disease and invasive mechanical ventilation: a randomized study | ||||||||||||||||||
Medical condition: coronavirus (covid-19) infection with respiratory failure requiring mechanical ventilation. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003915-11 | Sponsor Protocol Number: CarniValI (Uni-Koeln-1107) | Start Date*: 2009-09-24 | |||||||||||
Sponsor Name:University of Utah | |||||||||||||
Full Title: Phase I/II Trial of Valproic Acid and Carnitine in Infants with Spinal Muscular Atrophy Type I (CARNI-VAL Type I) | |||||||||||||
Medical condition: Spinal Muscular Atrophy Type I in infants | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005547-17 | Sponsor Protocol Number: RHMNUT0048 | Start Date*: 2010-01-28 |
Sponsor Name:Southampton University Hospital NHS Trust | ||
Full Title: Refeeding risks in patients requiring nutrition support. A twin centre double-blind randomised controlled trial of parenteral nutrition support. | ||
Medical condition: Patients who have a non-functioning gastrointestinal tract require artifical intravenous nutrition. This is usally a result recent surgery or sepsis causing a reversible short term paralysis of th... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004552-37 | Sponsor Protocol Number: 18CH052 | Start Date*: 2019-05-07 | |||||||||||
Sponsor Name:CHU SAINT-ETIENNE | |||||||||||||
Full Title: Dose Study of Tranexamic Acid in Total Hip Replacement to Reduce Postoperative Hemoglobin Loss. A Phase 2 Randomized Double-blind Monocentric Study | |||||||||||||
Medical condition: Arthropathy of Hip | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006878-23 | Sponsor Protocol Number: APHP200023 | Start Date*: 2022-08-12 |
Sponsor Name:Assistance Publique Hopitaux Paris - APHP | ||
Full Title: Efficacy of Ruxolitinib as first line treatment in primary haemophagocytic lymphohistiocytosis (HLH) in children: a Phase 2, multicentre, non-comparative study R-HLH | ||
Medical condition: • Patient with Haemophagocytic lymphohistiocytosis (HLH) or lymphohistiocytic syndrome | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2021-003570-31 | Sponsor Protocol Number: ONITT | Start Date*: 2021-07-19 | ||||||||||||||||||||||||||
Sponsor Name:St. Jude Children's Research Hospital | ||||||||||||||||||||||||||||
Full Title: A Randomized Phase I/II Study of Onivyde in Combination with Talazoparib or Temozolomide in Children and Young Adults with Recurrent Solid Malignancies and Ewing Sarcoma | ||||||||||||||||||||||||||||
Medical condition: EWING SARCOMA | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003285-40 | Sponsor Protocol Number: 2019PI117 | Start Date*: 2020-12-15 | |||||||||||
Sponsor Name:CHRU de Nancy | |||||||||||||
Full Title: Evaluation of the hemodynamic tolerance of potassium canrenoate in brain-dead organ donors: randomized controlled clinical trial "CANREO-PMO" | |||||||||||||
Medical condition: hemodynamic of patients in a state of cerebral death candidate for renal or multiple organ removal (including kidney) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002219-69 | Sponsor Protocol Number: CHUBX2019/49 | Start Date*: 2021-07-19 |
Sponsor Name:CHU de Bordeaux | ||
Full Title: Long-term iron chelation in the prevention of secondary degeneration after cerebral infarction | ||
Medical condition: Stroke | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001413-20 | Sponsor Protocol Number: SILCOR-COVID19 | Start Date*: 2020-04-07 |
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | ||
Full Title: Phase 2, randomized, open-label study to compare the efficacy and safety of siltuximab vs. corticosteroids in hospitalized patients with COVID19 pneumonia | ||
Medical condition: COVID19 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004651-20 | Sponsor Protocol Number: 402-C-1808 | Start Date*: 2020-02-13 | |||||||||||
Sponsor Name:Reata Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 3 Trial of the Efficacy and Safety of Bardoxolone Methyl in Patients with Autosomal Dominant Polycystic Kidney Disease | |||||||||||||
Medical condition: Autosomal dominant polycystic kidney disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) FR (Prematurely Ended) CZ (Completed) BE (Completed) ES (Prematurely Ended) IT (Prematurely Ended) HU (Prematurely Ended) DK (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004613-34 | Sponsor Protocol Number: NordLOTS protocol 1.4 | Start Date*: 2008-03-14 | ||||||||||||||||
Sponsor Name:The Centre for Child and Adolescent Mental Health, Eastern and Southern Norway (R.BUP) | ||||||||||||||||||
Full Title: Nordic Longterm OCD treatment Study: A Nordic Multicenter treatment study evaluating a stepped care model based on the "Expert Clinical Guidelines". The study is performed with no sponsor from phar... | ||||||||||||||||||
Medical condition: Obsessive Compulsive Disorder | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Ongoing) DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000632-34 | Sponsor Protocol Number: AAUH-ICU-01 | Start Date*: 2017-04-25 | ||||||||||||||||
Sponsor Name:Department of Anaesthesia and Intensive Care Medicine, Aalborg University Hospital | ||||||||||||||||||
Full Title: Handling oxygenation targets in adults with acute hypoxaemic respiratory failure in the intensive care unit: A randomised clinical trial of a lower versus a higher oxygenation target Addendum: Tri... | ||||||||||||||||||
Medical condition: Acute hypoxaemic respiratory failure in patients admitted to the intensive care unit Addendum: Acute hypoxaemic respiratory failure in patients admitted to the intensive care unit with COVID-19 | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) FI (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001490-15 | Sponsor Protocol Number: RIS-BMN-3001 | Start Date*: 2007-04-23 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V | |||||||||||||
Full Title: A randomized, double-blind, placebo- and active-controlled, parallel-group study to evaluate the efficacy and safety of risperidone long-acting injectable for the prevention of mood episodes in the... | |||||||||||||
Medical condition: Subjects with a diagnosos of bipolar I disorder who are currently experiencing a manic or mixed episode (YMRS>20 and CGI-S>/= 4 [moderate]) or who are between mood episodes (non-acute; YMRS<12 and ... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019418-25 | Sponsor Protocol Number: CAFQ056A2217 | Start Date*: 2010-07-20 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: An open-label treatment study to evaluate the safety, tolerability and efficacy of AFQ056 in Parkinson’s patients with L-dopa induced dyskinesias | |||||||||||||
Medical condition: pazienti con malattia di Parkinson con discinesie indotte dalla L-dopa. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) FR (Prematurely Ended) DE (Prematurely Ended) FI (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003331-36 | Sponsor Protocol Number: FER-Loxapine-2015-01 | Start Date*: 2016-03-16 | |||||||||||
Sponsor Name:FERRER INTERNACIONAL SA | |||||||||||||
Full Title: A Phase IV, Open-label, Non-randomized, Clinical Trial to Evaluate the Safety of self-administered ADASUVE(R) (Staccato loxapine for inhalation) in Agitated Patients outside the hospital setting | |||||||||||||
Medical condition: Mild-to-moderate agitation in adult patients with schizophrenia or bipolar disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) NO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000955-25 | Sponsor Protocol Number: ClinDiab-08 | Start Date*: 2017-05-12 | |||||||||||
Sponsor Name:Medical University of Graz | |||||||||||||
Full Title: A single-centre, open-label, randomized controlled trial of efficacy, safety and usability of a basal insulin algorithm incorporated in the GlucoTab system compared to standard care for glycaemic m... | |||||||||||||
Medical condition: Diabetes mellitus type 2 | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000918-38 | Sponsor Protocol Number: C0311002 | Start Date*: 2019-05-16 | |||||||||||
Sponsor Name:Pfizer Inc. | |||||||||||||
Full Title: A PHASE 3, RANDOMIZED, MULTICENTER, OPEN-LABEL, CROSSOVER STUDY ASSESSING SUBJECT PERCEPTION OF TREATMENT BURDEN WITH USE OF WEEKLY GROWTH HORMONE (SOMATROGON) VERSUS DAILY GROWTH HORMONE (GENOTROP... | |||||||||||||
Medical condition: Growth Hormone Deficiency in Children | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) SK (Completed) CZ (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
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