- Trials with a EudraCT protocol (2,056)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
2,056 result(s) found for: Health outcomes.
Displaying page 1 of 103.
| EudraCT Number: 2020-001542-19 | Sponsor Protocol Number: 20-PP-04 | Start Date*: 2020-07-22 | |||||||||||
| Sponsor Name:CHU NICE | |||||||||||||
| Full Title: A 12-Week Multicentre, Randomized, Blinded, Parallel-Group Study Comparing the Efficacy and Safety of Ixekizumab to Placebo in Patients > 6 years of age with EB simplex generalized severe | |||||||||||||
| Medical condition: Epidermolysis bullosa simplex | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-004764-18 | Sponsor Protocol Number: 01-17 | Start Date*: 2017-07-24 |
| Sponsor Name:St Patrick’s Mental Health Services | ||
| Full Title: Ketamine as an adjunctive therapy for Major Depression - a randomised controlled pilot trial: The KARMA-Dep Trial | ||
| Medical condition: Depression | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: IE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-003810-42 | Sponsor Protocol Number: Version2.0;18/12/2013 | Start Date*: 2016-06-24 | ||||||||||||||||
| Sponsor Name:University of Edinburgh (ACCORD) [...] | ||||||||||||||||||
| Full Title: A pragmatic group sequential placebo controlled randomised trial to determine the effectiveness of Glyceryl trinitrate for retained placenta (GOT-IT Trial) | ||||||||||||||||||
| Medical condition: Retained placenta | ||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2019-001077-87 | Sponsor Protocol Number: IJB-RT-HNC-001 | Start Date*: 2019-08-08 | |||||||||||
| Sponsor Name:Institut Jules Bordet | |||||||||||||
| Full Title: Patient reported outcomes in term of swallowing and quality of life after prophylactic versus reactive percutaneous endoscopic gastrostomy tube placement in advanced head and neck cancer patients t... | |||||||||||||
| Medical condition: advanced head and neck cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-005012-42 | Sponsor Protocol Number: 747-302 | Start Date*: 2016-01-05 | |||||||||||
| Sponsor Name:Intercept Pharmaceuticals Inc. | |||||||||||||
| Full Title: A Phase 4, Double Blind, Randomized, Placebo Controlled, Multicenter Study Evaluating the Effect of Obeticholic Acid on Clinical Outcomes in Subjects with Primary Biliary Cholangitis. The COBALT S... | |||||||||||||
| Medical condition: Primary Biliary Cholangitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) LT (Prematurely Ended) AT (Prematurely Ended) BE (Completed) DK (Prematurely Ended) FI (Prematurely Ended) GB (GB - no longer in EU/EEA) EE (Prematurely Ended) ES (Prematurely Ended) NL (Prematurely Ended) FR (Ongoing) DE (Completed) BG (Prematurely Ended) PT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-000535-23 | Sponsor Protocol Number: HCB/2021/0060 | Start Date*: 2022-06-20 | |||||||||||
| Sponsor Name:Barcelona Institute for Global Health (ISGlobal) | |||||||||||||
| Full Title: Efficacy of low dose acetylsalicylic acid in preventing adverse maternal and perinatal outcomes in SARS-CoV-2 infected pregnant women | |||||||||||||
| Medical condition: SARS-CoV-2 infection | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-024477-39 | Sponsor Protocol Number: 105MS302 | Start Date*: 2011-05-06 | |||||||||||
| Sponsor Name:Biogen Idec Limited | |||||||||||||
| Full Title: A Dose-Frequency Blinded, Multicenter, Extension Study to Determine the Long-Term Safety and Efficacy of PEGylated Interferon Beta-1a (BIIB017) in Subjects With Relapsing Multiple Sclerosis | |||||||||||||
| Medical condition: Relapsing Multiple Sclerosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: LV (Completed) BE (Completed) DE (Completed) ES (Completed) BG (Completed) EE (Completed) GB (Completed) GR (Completed) CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003278-37 | Sponsor Protocol Number: INSIGHT-014-ACTIV-3 | Start Date*: 2020-09-04 | ||||||||||||||||
| Sponsor Name:Regents of the University of Minesota | ||||||||||||||||||
| Full Title: A Multicenter, Adaptive, Randomized, Blinded Controlled Trial of the Safety and Efficacy of Investigational Therapeutics for Hospitalized Patients with COVID-19 | ||||||||||||||||||
| Medical condition: Subjects infected with SARS-CoV-2, admitted to the hospital due to COVID-19. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) GB (GB - no longer in EU/EEA) SE (Prematurely Ended) PL (Completed) GR (Completed) IT (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2017-002402-13 | Sponsor Protocol Number: R04684 | Start Date*: 2018-02-02 | |||||||||||
| Sponsor Name:Manchester University NHS Foundation Trust | |||||||||||||
| Full Title: A Randomised controlled trial to Evaluate the effectiveness and cost benefit of prescribing high dose FLuoride toothpaste in preventing and treating dEntal Caries in high-risk older adulTs (REFLECT... | |||||||||||||
| Medical condition: Dental caries in high-risk older adults | |||||||||||||
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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) | |||||||||||||
| EudraCT Number: 2016-004354-15 | Sponsor Protocol Number: DANPAPP | Start Date*: 2017-12-13 | ||||||||||||||||
| Sponsor Name: Rigshospitalet | ||||||||||||||||||
| Full Title: Prevalence, pattern and disease course of arthritis and enthesitis in patients with psoriasis, and the effect of apremilast in subclinical US-defined psoriatic arthritis - A population-based study ... | ||||||||||||||||||
| Medical condition: Psoriasis and psoriatic arthritis | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2020-002135-30 | Sponsor Protocol Number: NCT04379973 | Start Date*: 2021-04-28 |
| Sponsor Name:Antwerp University Hospital (UZA) | ||
| Full Title: Live birth after additional tubal flushing with oil-based contrast versus no additional flushing: a randomised, multicentre, parallel group pragmatic trial in infertile women with at least one pate... | ||
| Medical condition: Infertility defined as lack of conception despite 12 months of unprotected intercourse, or three cycles of donor insemination without pregnancy or three ovulatory ovulation induction cycles without... | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: BE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-002447-22 | Sponsor Protocol Number: C4671031 | Start Date*: 2022-11-21 | |||||||||||
| Sponsor Name:Pfizer Inc. | |||||||||||||
| Full Title: AN INTERVENTIONAL EFFICACY AND SAFETY, PHASE 2, DOUBLE BLIND, 2 ARM STUDY TO INVESTIGATE ORALLY ADMINISTERED NIRMATRELVIR/RITONAVIR COMPARED WITH PLACEBO/RITONAVIR FOR THE TREATMENT OF SEVERE COVID... | |||||||||||||
| Medical condition: SARS-CoV-2 Infection | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BG (Completed) SK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-004565-14 | Sponsor Protocol Number: ECP-002e | Start Date*: 2014-02-13 | |||||||||||
| Sponsor Name:Edimer Pharmaceuticals, Inc. | |||||||||||||
| Full Title: Extension Study of XLHED-Affected Male Subjects treated with EDI200 in Protocol ECP-002 | |||||||||||||
| Medical condition: X-linked hypohidrotic ectodermal dysplasia (XLHED) is caused by inherited defects in the ectodysplasin (EDA) gene that disrupt synthesis and/or function of the primary translational product EDA-A1.... | |||||||||||||
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| Population Age: Infants and toddlers, Under 18 | Gender: Male | ||||||||||||
| Trial protocol: DE (Completed) FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-000124-14 | Sponsor Protocol Number: NL47077 | Start Date*: 2014-10-21 |
| Sponsor Name:Academic Medical Center | ||
| Full Title: Antibiotic prophylaxis to prevent wound infections following implant removal after foot, ankle and lower leg fractures. | ||
| Medical condition: Postoperative wound infection following implant removal below the knee | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-004835-19 | Sponsor Protocol Number: 38RC16.015 | Start Date*: 2017-07-20 | |||||||||||
| Sponsor Name:University Hospital Grenoble | |||||||||||||
| Full Title: Dexamethasone in Herpes Simplex Virus Encephalitis Open label Randomized Controlled Trial with an Observer-blinded evaluation at 6 months | |||||||||||||
| Medical condition: HSV encephalitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-002248-34 | Sponsor Protocol Number: FInCH | Start Date*: 2018-02-20 | |||||||||||||||||||||
| Sponsor Name:King's College London | |||||||||||||||||||||||
| Full Title: FInCH Study: A randomised feasibility study comparing fluoride interventions to prevent dental decay in older people in care homes. | |||||||||||||||||||||||
| Medical condition: Prevention of dental decay in older people in care homes | |||||||||||||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2018-001904-12 | Sponsor Protocol Number: 18040 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:University of Nottingham | |||||||||||||
| Full Title: Desmopressin for reversal of Antiplatelet drugs in Stroke due to Haemorrhage (DASH) | |||||||||||||
| Medical condition: Intracerebral haemorrhage | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-000356-33 | Sponsor Protocol Number: oxy123 | Start Date*: 2013-03-27 | |||||||||||
| Sponsor Name:Västra Götaland | |||||||||||||
| Full Title: Delay in labour due to ineffective uterine contractions is still a major problem in modern obstetric care. It is one of the main reasons for the increased rate of operative deliveries, particularly... | |||||||||||||
| Medical condition: Labor dystocia (LD) also referred to as prolonged labour is a commonly identified problem in modern delivery care with three described possible causes: inefficient uterine action, occiputposterior ... | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: SE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-003075-11 | Sponsor Protocol Number: 9HB01EXT | Start Date*: 2011-12-05 | |||||||||||
| Sponsor Name:Biogen Idec Research Ltd | |||||||||||||
| Full Title: An Open-Label, Multicenter Evaluation of the Long-Term Safety and Efficacy of Recombinant, Human Coagulation Factor IX Fusion Protein (rFIXFc) in the Prevention and Treatment of Bleeding Episodes i... | |||||||||||||
| Medical condition: The medical condition to be investigated is Hemophilia B, or Christmas disease. Hemophilia B is a deficiency in the clotting FIX and is a recessively inherited coagulation disorder due to an X-chro... | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: GB (Completed) DE (Completed) BE (Completed) SE (Completed) PL (Completed) IT (Completed) IE (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-004424-65 | Sponsor Protocol Number: 15085MS-AS | Start Date*: 2016-05-09 |
| Sponsor Name:Belfast Health and Social Care Trust | ||
| Full Title: Prevention of post-operative complications by using HMG-CoA Reductase Inhibitor in patients undergoing oesophagectomy - A multicentre, randomised, double blind, placebo controlled trial | ||
| Medical condition: Post-operative complications - Post-operative Pulmonary complication, Acute Respiratory Distress Syndrome and Myocardial Infarction | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: View results | ||
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