- Trials with a EudraCT protocol (143)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (25)
143 result(s) found for: D2.
Displaying page 1 of 8.
EudraCT Number: 2022-002330-13 | Sponsor Protocol Number: COAM-CFD-01 | Start Date*: 2022-06-22 | |||||||||||
Sponsor Name:Fakultní nemocnice v Motole | |||||||||||||
Full Title: The randomized, double blind study phase III.b of the Comprehensive assessment of the musculoskeletal health in children with cystic fibrosis – on the search for means of improvement | |||||||||||||
Medical condition: musculoskeletal health in children with cystic fibrosis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001284-12 | Sponsor Protocol Number: PA-01 | Start Date*: 2014-11-19 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: The Role of the Dopamine D2 Receptor System in Pornographic Addiction – A [11C]-Raclopride PET Study | ||
Medical condition: pornographic addiction | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-006302-28 | Sponsor Protocol Number: OXYGENE | Start Date*: 2012-07-11 |
Sponsor Name:UNIVERSITA' DEGLI STUDI DI PARMA | ||
Full Title: Dopamine modulation of oxytocin prosocial effects | ||
Medical condition: HEALTHY VOLUNTEERS. FOR PATIENTS WITH AUTISM OR SCHIZOPHRENIA | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2010-024182-44 | Sponsor Protocol Number: NL3372110110 | Start Date*: 2011-01-12 | |||||||||||||||||||||
Sponsor Name: | |||||||||||||||||||||||
Full Title: Pilot study: Leucocyte actIvation and endothelial function after oral fat loading combined with VITamin D | |||||||||||||||||||||||
Medical condition: Endothelial function Leukocyte activation Triglyceride metabolism Skin autofluorescence | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002250-97 | Sponsor Protocol Number: NA | Start Date*: 2022-10-14 |
Sponsor Name:CHU de Liège | ||
Full Title: Comparison between periarticular infiltration, pericapsular nerve group block (PENG), and suprainguinal iliaca fascia block on postoperative functional recovery in total hip arthroplasty: a randomi... | ||
Medical condition: Total hip arthroplasty surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-001139-98 | Sponsor Protocol Number: IC2021-07 | Start Date*: 2022-06-13 | ||||||||||||||||
Sponsor Name:Institut Curie | ||||||||||||||||||
Full Title: Opioid-Free versus Opioid-Based Anaesthesia for secondary free-flap reconstruction surgery of the breast: A phase III multicentric randomized controlled study | ||||||||||||||||||
Medical condition: Anaesthesia during secondary free flap reconstruction surgery of the breast. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004062-41 | Sponsor Protocol Number: D2PET-2007 | Start Date*: 2007-08-13 |
Sponsor Name:Jarmo Hietala | ||
Full Title: Effect differences of conventional and newer atypical antipsychotics – Perphenazine and brain dopamine D2 receptor blockade | ||
Medical condition: Tutkittavat ovat terveitä. | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005097-66 | Sponsor Protocol Number: NCAG2512 | Start Date*: 2014-07-14 |
Sponsor Name:HOMVIORA Arzneimittel - Dr. Hagedorn GmbH & Co. | ||
Full Title: Effect of two homeopathic preparations on blood pressure in comparison to metoprolol (trade name Beloc-Zok® mite 47,5 mg) in 90 patients suffering from mild hypertonia. A prospective, confirmator... | ||
Medical condition: Patients suffering from mild hypertonia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-004469-11 | Sponsor Protocol Number: PP-SA-001 | Start Date*: 2022-01-11 |
Sponsor Name:PHERECYDES PHARMA | ||
Full Title: PhagoDAIR I: A Phase I/II Multicenter, Randomized, Double-Blind Study to Evaluate Efficacy and Safety of Phage Therapy in Patients with Hip or Knee Prosthetic Joint Infection due to Staphylococcus ... | ||
Medical condition: knee or hip prosthetic joint infection (PJI) due to Staphylococcus aureus, with the indication of DAIR and Suppressive Antibiotics Therapy (SAT | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004905-15 | Sponsor Protocol Number: DNDi-FEX-12-CH | Start Date*: 2017-09-13 |
Sponsor Name:Drugs for Neglected Diseases initiative (DNDi) | ||
Full Title: Phase 2 Randomized, Multicenter, Double-blinded Safety and Efficacy Study to Evaluate Oral Fexinidazole Dosing Regimens for the Treatment of Adult Patients with Chronic Indeterminate Chagas Disease | ||
Medical condition: Chagas disease (CD) is a disease caused by Trypanosoma cruzi, ranking among the world’s most neglected diseases. There is significant associated morbidity and mortality, particularly in chronic ph... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-002460-13 | Sponsor Protocol Number: VITDALIZE | Start Date*: 2017-01-03 |
Sponsor Name:Medical University of Graz | ||
Full Title: Effect of high-dose vitamin D3 on 28-day mortality in adult critically ill patients with severe vitamin D deficiency: a multicenter, placebo-controlled double-blind phase III RCT | ||
Medical condition: Adult critically ill patients with severe vitamin D deficiency | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004554-42 | Sponsor Protocol Number: TAMDMD | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:University of Basel Children's Hospital, Division of Neuropediatrics | |||||||||||||
Full Title: Tamoxifen in Duchenne muscular dystrophy: A multicenter, randomised, double-blind, placebo-controlled, phase 3 safety and efficacy 48-week trial Tamoxifen in Duchenne muscular dystrophy: A 48-week... | |||||||||||||
Medical condition: Duchenne muscular dystrophy | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (GB - no longer in EU/EEA) FR (Completed) ES (Prematurely Ended) NL (Prematurely Ended) BE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011264-11 | Sponsor Protocol Number: 25021960 | Start Date*: 2009-12-22 | |||||||||||
Sponsor Name:Queen Mary University of London
[...]
1. Queen Mary University of London
2. Medical Research Council |
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Full Title: A randomized, double blind, placebo controlled, phase II, multi-centre pilot study to investigate the effects of vitamin D2 or D3 supplementation on metabolic parameters in people at risk of type 2... | |||||||||||||
Medical condition: Preventing/ delaying the onset of type 2 diabetes mellitus and cardiovascular risk factors. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001748-39 | Sponsor Protocol Number: PHRC2013-01 | Start Date*: 2014-08-21 |
Sponsor Name:CHU d'Angers | ||
Full Title: TRAnexamic Acid for Preventing postpartum hemorrhage following a vaginal delivery : a multicenter randomised, double blind placebo controlled trial | ||
Medical condition: postpartum hemorrhage | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-006787-11 | Sponsor Protocol Number: 0819D1522 | Start Date*: 2009-01-15 | |||||||||||
Sponsor Name:Shionogi & Co., Ltd. | |||||||||||||
Full Title: A randomized, double blind, placebo-controlled, 2-period cross over study to evaluate effects of S-555739 on prostaglandin D2 (PGD2) induced nasal airway resistance in healthy adult volunteers | |||||||||||||
Medical condition: Allergic rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003816-38 | Sponsor Protocol Number: PHRC-N/2017-FJ-01 | Start Date*: 2020-11-09 | |||||||||||
Sponsor Name:CHU DE NIMES | |||||||||||||
Full Title: Add-on buprenorphine at analgesic doses for the treatment of severe suicidal ideas during a major depressive episode | |||||||||||||
Medical condition: Treatment of severe suicidal ideas in patients suffers from a current major depressive episode | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004748-36 | Sponsor Protocol Number: PA-CL-03A | Start Date*: 2008-10-30 | |||||||||||
Sponsor Name:Vifor (International) Inc. | |||||||||||||
Full Title: An open-label, randomized, active controlled multi center phase II dose finding study to evaluate the ability of PA21 to lower serum phosphate levels and the tolerability in patients with chronic k... | |||||||||||||
Medical condition: Hyperphosphatemia in patients with chronic kidney disease on maintenance hemodialysis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004729-25 | Sponsor Protocol Number: 9741 | Start Date*: 2006-04-14 |
Sponsor Name:R & D Directorate,Central Manchester and Manchester Children's University Hospitals NHS Trust | ||
Full Title: A pilot randomised controlled trial to determine if vitamin D treatment will result in a greater bone mass acquisition in pubertal girls | ||
Medical condition: Hypovitaminosis D in healthy subjects / Subclinical vitamin D deficiency. Recently there have been many reports of vitamin D deficiency in healthy adolescents worldwide. It is not yet known wheth... | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-000831-34 | Sponsor Protocol Number: GoforGH | Start Date*: 2022-01-11 |
Sponsor Name:Medical University of Vienna | ||
Full Title: InvestiGating the rOle of Growth Hormone in hepatic lipid metabolism in humans | ||
Medical condition: Healthy subjects | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001492-33 | Sponsor Protocol Number: CGE_2020_9 | Start Date*: 2020-04-10 |
Sponsor Name:Hôpital Fondation Adolphe de Rothschild | ||
Full Title: Interest in the administration of Dornase alpha aerosol in ARDS secondary to respiratory infection by the coronavirus SRASCoV-2 / COVID-19 | ||
Medical condition: Patients on mechanical ventilation, inpatient resuscitation for ARDS, secondary to COVID-19 infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
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