- Trials with a EudraCT protocol (2,310)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
2,310 result(s) found.
Displaying page 1 of 116.
EudraCT Number: 2012-000309-60 | Sponsor Protocol Number: 120101 | Start Date*: 2016-03-30 | |||||||||||
Sponsor Name:Göteborgs universitet | |||||||||||||
Full Title: Biochemical and neuropsychological effects on Premenstrual Dysphoric Disorder after acute administration of escitalopram | |||||||||||||
Medical condition: Premenstrual Dysphoric Disorder | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002112-41 | Sponsor Protocol Number: 2016-05-04 | Start Date*: 2016-07-16 |
Sponsor Name:Region Östergötland | ||
Full Title: Can Insuline improve the healing of dental implants? | ||
Medical condition: Missing teeth | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004376-64 | Sponsor Protocol Number: EURO17-09 | Start Date*: 2018-01-10 | |||||||||||
Sponsor Name:Eurocine Vaccines AB | |||||||||||||
Full Title: A Phase I/II, randomised, multicentre, placebo-controlled, partially-blinded, parallel-group study to assess the safety, tolerability and immune response following vaccination with ImmunoseTM FLU i... | |||||||||||||
Medical condition: Influenza | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002506-37 | Sponsor Protocol Number: SANNI-project:03 | Start Date*: 2020-01-08 |
Sponsor Name:Region Skane | ||
Full Title: Dexmedetomidine for analgosedation to newborn infants during neonatal intensive care – a prospective pharmacokinetic/ pharmacodynamic/ pharmacogenetic observational study.Cohort 3 in The SANNI Pr... | ||
Medical condition: Sick newborn infants in need of intensive care. | ||
Disease: | ||
Population Age: Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-001417-79 | Sponsor Protocol Number: DIAGNODE-1 | Start Date*: 2018-02-05 | |||||||||||
Sponsor Name:Linköping University | |||||||||||||
Full Title: Open Label Pilot Trial in patients with recent-onset T1D to evaluate the safety, diabetes status and immune response of GAD-antigen (Diamyd®) therapy administered into lymph nodes in combination wi... | |||||||||||||
Medical condition: Type 1 diabetes | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001373-33 | Sponsor Protocol Number: 2016-3 | Start Date*: 2017-02-17 |
Sponsor Name:Region Ostergotland | ||
Full Title: Clinical Study Protocol An open phase IV,RCT, evaluating patient controlled sedation, in three different dosages of propofol in healthy subjects undergoing elective gynaecological out-patient su... | ||
Medical condition: Gynecological outpatient surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-002008-28 | Sponsor Protocol Number: 2017-002008-28 | Start Date*: 2017-12-21 | |||||||||||
Sponsor Name:Region Skåne | |||||||||||||
Full Title: A prospective open label study to evaluate treatment of chronic HCV infection with glecaprevir/pibrentasvir in PWID attending a needle exchange program | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004279-11 | Sponsor Protocol Number: B7471007 | Start Date*: 2019-02-27 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A PHASE 3, RANDOMIZED, DOUBLE-BLIND TRIAL TO EVALUATE THE SAFETY AND IMMUNOGENICITY OF A 20-VALENT PNEUMOCOCCAL CONJUGATE VACCINE IN PNEUMOCOCCAL VACCINE–NAÏVE ADULTS 18 YEARS OF AGE AND OLDER | |||||||||||||
Medical condition: Pneumococcal Infections | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003106-16 | Sponsor Protocol Number: B2 | Start Date*: 2016-08-03 |
Sponsor Name:Antonis Valachis | ||
Full Title: Immunogenicity of influenza vaccination among breast cancer patients treated with trastuzumab in adjuvant setting | ||
Medical condition: Efficacy of vaccination against influenza in patients with breast cancer treated with Trastuzumab as adjuvant therapy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-005046-55 | Sponsor Protocol Number: 20151104 | Start Date*: 2016-08-23 |
Sponsor Name:Umeå University Hospital | ||
Full Title: Evaluation of [68Ga]PSMA PET/MRI in intermediate and high risk prostate cancer – a comparison with mpMRI, [11C]ACE PET/CT and histopathological validation | ||
Medical condition: Medium and high risk prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-018594-37 | Sponsor Protocol Number: EMN-alloRIC2010 | Start Date*: 2013-01-24 | ||||||||||||||||
Sponsor Name:European Myeloma Network | ||||||||||||||||||
Full Title: European Myeloma Network sequential phase I / phase II trial on RIC allogeneic transplantation: an optimized program for high risk relapsed patients | ||||||||||||||||||
Medical condition: Allogeneic transplantation for patients with multiple myeloma | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006042-32 | Sponsor Protocol Number: GE-067-019 | Start Date*: 2012-09-12 | |||||||||||
Sponsor Name:GE Healthcare Ltd and its affiliates | |||||||||||||
Full Title: A Single-Arm Open-Label Multi-Center Study to Determine the Test-Retest Variability of PET Brain Imaging with Flutemetamol (18F) Injection. | |||||||||||||
Medical condition: Subjects with amnestic Mild Cognitive Impairment (aMCI) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004940-31 | Sponsor Protocol Number: IMM-12-0074 | Start Date*: 2013-06-27 | |||||||||||
Sponsor Name:Dept of medical sciences, Rheumatology | |||||||||||||
Full Title: Dermal inflammation in psoriatic arthritis, the association to molecular mass of hyaluronan and effect of adalimumab. A prospective, open-label, multi-center study of hyaluronan molecular mass dis... | |||||||||||||
Medical condition: Active psoriatic arthritis according to CASPAR | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003743-30 | Sponsor Protocol Number: BEVPAC | Start Date*: 2012-11-20 |
Sponsor Name:Karolinska University Hospital | ||
Full Title: A prospective randomized Phase II study to identify predictive biomarkers and mechanisms of therapy resistance in patients with HER2-negative metastatic breast cancer (MBC) treated with the combina... | ||
Medical condition: Advanced breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-002217-19 | Sponsor Protocol Number: 232100-0024 | Start Date*: 2012-12-13 |
Sponsor Name:Dept of Surgery [...] | ||
Full Title: Postoperative treatment with Vitamin D for patients with a history of Bariatric Surgery in C and U County. | ||
Medical condition: Hypovitaminosis D after bariatric surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003479-20 | Sponsor Protocol Number: 2011/433 | Start Date*: 2013-04-15 | |||||||||||
Sponsor Name:Handkirurgiska kliniken, Universitetssjukhuset Örebro | |||||||||||||
Full Title: Lateral humerus epicondylitis- a clinical, muscle morpological, muscle metabolical and functional evaluation of a new model for treatment. | |||||||||||||
Medical condition: Chronic lateral humerus epiconcylitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005660-18 | Sponsor Protocol Number: PH-IUD-01 | Start Date*: 2012-03-26 | |||||||||||
Sponsor Name:Pharmanest AB | |||||||||||||
Full Title: An open label pharmcokinetic study of a topical formulation of lidocaine (SHACT) for pain relief in women receiving an Intra Uterine Device. | |||||||||||||
Medical condition: Pain during insertion of an intra uterine device | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000721-53 | Sponsor Protocol Number: ITT-PMSExt | Start Date*: 2012-12-07 | |||||||||||
Sponsor Name:Dept of Neurology, Umeå University Hospital, Umeå, Sweden | |||||||||||||
Full Title: ITT-PMS Extension An extension study of intrathecal therapy with monoclonal antibodies in progressive multiple sclerosis | |||||||||||||
Medical condition: Secondary progressive multiple sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004646-42 | Sponsor Protocol Number: 05PF1311 | Start Date*: 2014-03-17 | |||||||||||
Sponsor Name:Q-MED AB | |||||||||||||
Full Title: A randomized, evaluator-blinded, comparative study to evaluate the efficacy and safety of different injection volumes of botulinum toxin type A, Azzalure®, in the glabellar lines. | |||||||||||||
Medical condition: Glabella frown lines | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002690-22 | Sponsor Protocol Number: OXYPEP003 | Start Date*: 2013-08-21 | |||||||||||
Sponsor Name:PeP-Tonic Medical AB | |||||||||||||
Full Title: A pharmacokinetic study of vaginally and intravenously administered oxytocin in postmenopausal women with vaginal atrophy | |||||||||||||
Medical condition: Vaginal atrophy in postmenopausal women | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
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