- Trials with a EudraCT protocol (28,960)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
28,960 result(s) found for: Informed Consent.
Displaying page 712 of 1,448.
| EudraCT Number: 2015-000841-22 | Sponsor Protocol Number: HZA107112 | Start Date*: 2015-08-04 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research and Development Ltd | |||||||||||||
| Full Title: A randomised, double-blind, two-way crossover study to investigate the effect of inhaled fluticasone furoate on short-term growth in paediatric subjects with asthma | |||||||||||||
| Medical condition: Chronic disease of the lungs characterized by airway inflammation, bonchoconstriction and increased airway responsiveness. | |||||||||||||
|
|||||||||||||
| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-004178-40 | Sponsor Protocol Number: B1841008 | Start Date*: 2015-04-03 |
| Sponsor Name:Pfizer, Inc. | ||
| Full Title: A Phase 4, Open-label Trial to Assess the Safety, Tolerability, and Immunogenicity of Prevenar in Older Infants and Young Children in China Who Are Naive to Previous Pneumococcal Vaccination | ||
| Medical condition: Pneumococcal Infections | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2014-004177-16 | Sponsor Protocol Number: B1841007 | Start Date*: 2015-04-09 |
| Sponsor Name:Pfizer Japan, Inc. | ||
| Full Title: A Phase 4, Randomized, Open-Label Trial Evaluating the Safety, Tolerability, and Immunogenicity of DTaP Vaccine in Healthy Infants Given With a 7-valent Pneumococcal Conjugate Vaccine in Japan. | ||
| Medical condition: Prevention of disease caused by a type of bacteria called Streptococcus pneumoniae (pneumococcal disease). | ||
| Disease: | ||
| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2013-000797-30 | Sponsor Protocol Number: SPI-IIT-002 | Start Date*: 2013-10-08 | |||||||||||||||||||||
| Sponsor Name:Department of Medical Research, Odense University Hospital, Svendborg Hospital | |||||||||||||||||||||||
| Full Title: Inhibition of aldosterone to diminish diffuse myocardial fibrosis in atrial fibrillation | |||||||||||||||||||||||
| Medical condition: Paroxysmal and persistent atrial fibrillation | |||||||||||||||||||||||
|
|||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2018-004519-31 | Sponsor Protocol Number: ENTERL08784 | Start Date*: 2019-01-31 | |||||||||||
| Sponsor Name:Sanofi | |||||||||||||
| Full Title: Randomized, placebo-controlled, clinical trial to evaluate the efficacy of probiotic Bacillus clausii in the treatment of pediatric patients with irritable bowel syndrome | |||||||||||||
| Medical condition: Irritable bowel syndrome | |||||||||||||
|
|||||||||||||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002611-29 | Sponsor Protocol Number: MEL001 | Start Date*: 2012-04-04 |
| Sponsor Name:Freistaat Bayern | ||
| Full Title: A prospective phase I and consecutive phase II, twoarm, randomized multi-center trial of temsirolimus in combination with pioglitazone, etoricoxib and metronomic low-dose trofosfamide versus dacarb... | ||
| Medical condition: metastatic melanoma or metastatic uveal carcinoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-005886-15 | Sponsor Protocol Number: VASOCONTROL-I | Start Date*: 2021-07-21 |
| Sponsor Name:University Medical Center Groningen | ||
| Full Title: Evaluation of pharmacokinetic and –dynamic characteristics of norepinephrine for the augmentation of arterial blood pressure in healthy volunteers prior to and during general anesthesia | ||
| Medical condition: Bloodpressure during anaesthesia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-004290-19 | Sponsor Protocol Number: SP873 | Start Date*: 2006-01-25 | |||||||||||
| Sponsor Name:Schwarz Biosciences GmbH | |||||||||||||
| Full Title: A double-blind, placebo-controlled, parallel group, proof of concept trial to assess the tolerabiltiy, safety and efficacy of rotigotine nasal spray for the acute treatment of 'off' symptoms in sub... | |||||||||||||
| Medical condition: advanced-stage, idiopathic Parkinson's disease | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) GB (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005474-31 | Sponsor Protocol Number: AT305-X-06-004 | Start Date*: 2008-02-25 | |||||||||||
| Sponsor Name:Akros Pharma Inc. | |||||||||||||
| Full Title: A Phase 2, Randomized, Double-blind, Placebo-controlled, Parallel Group Study Evaluating the Efficacy and Safety of JTT-305 Administered for Six Months in Postmenopausal Women with Osteoporosis | |||||||||||||
| Medical condition: Osteoporosis in postmenopausal women | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-000730-19 | Sponsor Protocol Number: HEEL-2011-02 | Start Date*: 2012-08-23 | |||||||||||
| Sponsor Name:Radboud University Nijmegen Medical Centre | |||||||||||||
| Full Title: The analgesic efficacy of Δ9-THC (Namisol®) in Chronic Pancreatitis Patients Suffering From Persistent Abdominal Pain: a Randomized, Double-blinded, Placebo-controlled, Parallel Design | |||||||||||||
| Medical condition: Chronic pancreatitis with persistant abdominal pain | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-000812-27 | Sponsor Protocol Number: HEEL-2011-03 | Start Date*: 2012-07-19 | ||||||||||||||||
| Sponsor Name:Radboud University Nijmegen Medical Centre | ||||||||||||||||||
| Full Title: The analgesic efficacy of Δ9-THC (Namisol®) in patients with persistent postsurgical abdominal pain: a randomized, double-blinded, placebo-controlled, parallel design’ | ||||||||||||||||||
| Medical condition: Patients with persistent postsurgical abdominal pain | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-000928-18 | Sponsor Protocol Number: PROMESA | Start Date*: 2013-11-21 |
| Sponsor Name:Hospital of the Ludwig-Maximilians-University of Munich | ||
| Full Title: Double blind, randomised, prospective placebo controlled parallel group phase III study to investigate the Effect of EGCG supplementation on disease progression of patients with Multiple System Atr... | ||
| Medical condition: Progression of patients with Multiple System Atrophy (MSA) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-000358-65 | Sponsor Protocol Number: A00394 | Start Date*: 2005-11-21 | |||||||||||
| Sponsor Name:UCB Pharma S.A. | |||||||||||||
| Full Title: A multicentre, double-blind, two parallel groups, randomized trial over four weeks of treatment to compare the clinical efficacy and safety of Levocetirizine 5 mg oral capsules once daily in the mo... | |||||||||||||
| Medical condition: Chronic Idiopathic Urticaria | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) GB (Completed) ES (Completed) IT (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-000476-13 | Sponsor Protocol Number: SP738 | Start Date*: 2004-08-10 |
| Sponsor Name:Schwarz Biosciences GmbH | ||
| Full Title: LONG-TERM OPEN-LABEL EXTENSION TRIAL FOR SUBJECTS COMPLETING THE PHASE 3 TRIAL OF FESOTERODINE (SP583) FOR THE TREATMENT OF OVERACTIVE BLADDER SYNDROME | ||
| Medical condition: overactive bladder | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-023324-25 | Sponsor Protocol Number: ABCSG32 | Start Date*: 2011-03-31 |
| Sponsor Name:ABCSG (Austrian Breast & Colorectal Cancer Study Group) | ||
| Full Title: Multicentre randomized phase II study of neoadjuvant trastuzumab plus docetaxel with and without bevacizumab and trastuzumab plus docetaxel plus non-pegylated liposome-encapsulated doxorubicin (NPL... | ||
| Medical condition: HER2-positive, adenocarcinoma of the breast (except inflammatory breast cancer, T4d) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-004969-40 | Sponsor Protocol Number: RHFERAMH-0001 | Start Date*: 2012-11-27 | |||||||||||
| Sponsor Name:Fertility Clinic, Copenhagen University Hospital, Rigshospitalet | |||||||||||||
| Full Title: An AMH based indivdualised controlled ovarian stimulation regiment using Corifollitrophin or graded doses of rFSH versus a standard protocol. A randomised controlled trial | |||||||||||||
| Medical condition: In vitro fertilization include controlled ovarian stimulation (COS), where follicles are stimulated to full maturity. One of the main problems of the IVF treatment is still to some patients deve... | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-002015-17 | Sponsor Protocol Number: 2016-002015-17 | Start Date*: 2017-03-10 | |||||||||||
| Sponsor Name:Odense University Hospital | |||||||||||||
| Full Title: Low-flow Low-gradient Aortic Stenosis – Diagnostic Usefullness of Ivabradine | |||||||||||||
| Medical condition: Aortic valve stenosis with reduced ejection fraction | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-002421-37 | Sponsor Protocol Number: A4291043 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Pfizer Ltd., Ramsgate Road, Sandwich, Kent, CT13 9NJ, UK | |||||||||||||
| Full Title: A PHASE 2, 12 WEEK, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO- CONTROLLED, PARALLEL GROUP, PROOF OF CONCEPT STUDY EVALUATING THE EFFICACY AND SAFETY OF PD 0299685 FOR THE TREATMENT OF SYMPTOMS... | |||||||||||||
| Medical condition: INTERSTITIAL CYSTITIS/PAINFUL BLADDER SYNDROME. | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) DK (Completed) FR (Completed) FI (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019009-40 | Sponsor Protocol Number: A7331010 | Start Date*: 2010-07-08 | |||||||||||
| Sponsor Name:Pfizer, S.A. | |||||||||||||
| Full Title: Estudio clínico de Fase 2A, multicéntrico aleatorizado, doble ciego, controlado con placebo y con un fármaco activo, de diseño cruzado con dos cohortes y dos dosis, para la evaluación de la eficaci... | |||||||||||||
| Medical condition: Tratamiento del vasospasmo en el fenómeno de Raynaud primario y secundario. | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) SE (Completed) CZ (Completed) DE (Completed) HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-004667-61 | Sponsor Protocol Number: SUITE - CUOG-TE 05 | Start Date*: 2007-02-22 | |||||||||||
| Sponsor Name:Universitätsklinikum Hamburg-Eppendorf | |||||||||||||
| Full Title: Prospective open-labeled non randomized Phase-II study of SU011248 (Sunitinib) in male patients with relapsed or cisplatin-refractory germ cell cancer - A CUOG/GTCSG cooperative phase II study | |||||||||||||
| Medical condition: germ cell cancer | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: DE (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.