- Trials with a EudraCT protocol (1,163)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,163 result(s) found for: Healthy Volunteers.
Displaying page 39 of 59.
| EudraCT Number: 2009-016789-10 | Sponsor Protocol Number: 02-04-80 | Start Date*: 2010-02-19 |
| Sponsor Name:Div KIR AMC | ||
| Full Title: Efficacy of the H1N1 Flu (swine flu) vaccination in patients with Rheumatoid Arthritis treated with rituximab | ||
| Medical condition: To assess the efficacy of A/H1N1 vaccination in patients treated with rituximab therapy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-021879-85 | Sponsor Protocol Number: 10050 | Start Date*: 2010-09-08 |
| Sponsor Name:University of Nottingham | ||
| Full Title: Mode of action of Moviprep:impact on distribution of intestinal fluid and colonic microbiota | ||
| Medical condition: for bowel cleansing prior to any clinical procedure requiring a clean bowel, e.g, bowel endoscopy, lower gastrointestinal tract radiology or digestive tract surgery. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-002799-41 | Sponsor Protocol Number: SHRTRM3 | Start Date*: 2007-08-15 |
| Sponsor Name:Salford Royal Hospitals Trust [...] | ||
| Full Title: Iontophoresis as a possible therapy for digital ischaemia - preliminary studies in patients with scleroderma spectrum disorders | ||
| Medical condition: Digital ischaemia/ulceration in patients with scleroderma-spectrum disorders | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-002069-30 | Sponsor Protocol Number: 13069 | Start Date*: 2008-12-05 |
| Sponsor Name:Bayer Vital GmbH | ||
| Full Title: A randomized, double-blind, single centre, placebo-controlled pilot study to assess on a molecular level the influence of a 5 % dexpanthenol ointment in subjects with previously injured skin by inv... | ||
| Medical condition: Biopsy wounds on healthy volunteers | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-018181-36 | Sponsor Protocol Number: 09117 | Start Date*: 2010-02-23 |
| Sponsor Name:University of Nottingham | ||
| Full Title: Nitrous Oxide and Functional Magnetic Resonance Imaging to investigate cerebral regional blood flow, cerebral metabolism and neuronal activity. | ||
| Medical condition: This is part of a series of studies investigating the potential therapeutic use of low dose nitrous oxide in the treatment of cerebral vasospasm, a condition which occurs following brain injury and... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-002996-18 | Sponsor Protocol Number: ATI-2042-CLN-08 | Start Date*: 2005-03-10 | |||||||||||
| Sponsor Name:ARYx Therapeutics Limited | |||||||||||||
| Full Title: A Phase 2 Pilot Study of the Efficacy of ATI-2042 in subjects with Paroxysmal Atrial Fibrillation and Pacemakers | |||||||||||||
| Medical condition: Paroxysmal Atrial Fibrillation | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-000451-14 | Sponsor Protocol Number: 112896 | Start Date*: 2017-06-01 |
| Sponsor Name:GlaxoSmithKline Biologicals | ||
| Full Title: An open, single group, multi-centric, post marketing surveillance (PMS) to monitor the reactogenicity and safety of oral live attenuated human rotavirus (HRV) vaccine, Rotarix when administered acc... | ||
| Medical condition: Healthy volunteers (Active immunisation of infants from the age of 6 weeks for prevention of gastroenteritis due to rotavirus infection). | ||
| Disease: | ||
| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2012-001453-74 | Sponsor Protocol Number: Version01.1. | Start Date*: 2012-05-15 |
| Sponsor Name:Institute of Specific Prophylaxis and Tropical Medicine | ||
| Full Title: Comparison of vaccination routes: subcutaneus versus intramuscular application of FSME-Immun® | ||
| Medical condition: TBE vaccine (FSME-Immun®) is registered for intra-muscular application. Due to medical reasons (e.g. anticoagulant therapy, adipositas) intra-muscular application is not always possible. The aim o... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-023300-27 | Sponsor Protocol Number: JE-Boost | Start Date*: 2010-12-09 |
| Sponsor Name:Helsinki University Central Hospital | ||
| Full Title: Ability of the new Vero-cell-derived inactivated Japanese encephalitis vaccine (IXIARO) to elicit a booster response in travellers previously vaccinated with traditional mouse-brain derived vaccine... | ||
| Medical condition: The study subjects are healthy travelers and have no major chronic illnesses. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-004482-33 | Sponsor Protocol Number: THC-phMRI | Start Date*: 2007-07-31 | |||||||||||
| Sponsor Name:University Medical Center Utrecht | |||||||||||||
| Full Title: Investigating the acute effects of THC on functional brain systems | |||||||||||||
| Medical condition: This research project will be performed with healthy volunteers in order to determine whether THC modulates activity in functional brain systems. | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-022899-32 | Sponsor Protocol Number: TH0918 | Start Date*: 2011-01-19 | |||||||||||
| Sponsor Name:Celerion | |||||||||||||
| Full Title: An open label, randomised, single dose, 5 way cross over study to compare the rate and extent of absorption of a 8.75mg Flurbiprofen lozenge with flavour and excipient base variants of a 8.75mg Fl... | |||||||||||||
| Medical condition: Sore throat | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-000978-68 | Sponsor Protocol Number: | Start Date*: 2006-12-18 |
| Sponsor Name:AstraZeneca | ||
| Full Title: Treatment of systemic effects in patients with COPD | ||
| Medical condition: Chronic obstructive pulmonary disease (COPD) is a preventable and treatable disease state characterized by airflow limitation that is not fully reverible. The airflow limitation is usually progress... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-022772-31 | Sponsor Protocol Number: 20100812v2 | Start Date*: 2011-02-09 | |||||||||||
| Sponsor Name:Medizinische Universität Wien, Universitätsklinik für Psychiatrie und Psychotherapie | |||||||||||||
| Full Title: Brain Network Dysfunction as a Model for Schizophrenia: Connectivity Alterations using Ketamine and pharmacological Magnetic Resonance Imaging | |||||||||||||
| Medical condition: Quantify changes of resting-state functional connectivity in response to Esketamine in healthy volunteers. | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-024191-25 | Sponsor Protocol Number: CL3-20098-080 | Start Date*: 2012-03-30 | |||||||||||
| Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
| Full Title: Effects of agomelatine (25 to 50 mg/day) on circadian rhythms in patients with Major Depressive Disorder. An exploratory 6-week open, flexible dose, international multicentre, non comparative study. | |||||||||||||
| Medical condition: Major Depressive Disorder | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-004039-21 | Sponsor Protocol Number: 103366 | Start Date*: 2015-05-20 |
| Sponsor Name:GlaxoSmithKline | ||
| Full Title: An open, multicentric, post-marketing surveillance study to evaluate the safety and reactogenicity of GlaxoSmithKline Biologicals’ live attenuated oral Human Rotavirus (HRV) vaccine, Rotarix when a... | ||
| Medical condition: Healthy volunteers (Rotarix is indicated for the prevention of gastro-enteritis caused by Rotavirus, G1 and non G1 serotypes (such as G2, G3, G4, G9)) | ||
| Disease: | ||
| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2019-001869-32 | Sponsor Protocol Number: 24042019 | Start Date*: 2020-01-29 |
| Sponsor Name:Radboudumc | ||
| Full Title: Nano-MRI to visualize pancreatic inflammation in individuals with recent-onset type 1 diabetes | ||
| Medical condition: Type 1 Diabetes | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-002474-36 | Sponsor Protocol Number: IC51-301 | Start Date*: 2005-04-20 |
| Sponsor Name:Intercell AG | ||
| Full Title: Observer blinded, randomized Phase III study to investigate the non-inferiority of IC51 (JE-PIV) vs. JE-VAX as vaccines for japanese encephalitis in healthy volunteers | ||
| Medical condition: Japanese encephalitis (JE) is the most common viral encephalitis, with over 50,000 cases reported annually. It is a considerable public health problem for many Asian countries (WHO 1997). Close to ... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-005363-34 | Sponsor Protocol Number: EC/2008/50/FAHS | Start Date*: 2009-03-10 | |||||||||||
| Sponsor Name:University of Surrey | |||||||||||||
| Full Title: Investigation to explore whether there is a synergistic effect between nicotine replacement therapy and guided bodyscanning on cigarette cravings and withdrawal symptoms in temporarily abstinent sm... | |||||||||||||
| Medical condition: Healthy volunteers who currently smoke 10 or more cigarettes per day, for the last 3 years. The trial intends to explore whether there is a synergistic effect between the relaxation technique of g... | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-018596-24 | Sponsor Protocol Number: 6311 | Start Date*: 2011-05-19 |
| Sponsor Name:Oxford Radcliffe Hospital NHS Trust | ||
| Full Title: Assessment of Salmonella Typhim Vi(TM) vaccine (Sanofi Pasteur MSD) for the investigation of selective antibody deficiency to polysaccharide. | ||
| Medical condition: Suspected primary antibody deficiency states will be investigated | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-015679-28 | Sponsor Protocol Number: RHM CHI0499 | Start Date*: 2010-09-29 | |||||||||||
| Sponsor Name:Southampton University Hospitals Trust | |||||||||||||
| Full Title: PRIMARY PREVENTION OF ATOPY AND ASTHMA WITH ALLERGEN SUBLINGUAL IMMUNOTHERAPY | |||||||||||||
| Medical condition: Development of atopy | |||||||||||||
|
|||||||||||||
| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
| Download Options: | |
|---|---|
| Number of Trials to download: | |
| Download Content: | |
| Download Format: | |
| Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. | |
Query did not match any studies.