- Trials with a EudraCT protocol (105)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
105 result(s) found for: Validity.
Displaying page 1 of 6.
EudraCT Number: 2018-001758-89 | Sponsor Protocol Number: PSA-ULTRA | Start Date*: 2019-08-08 |
Sponsor Name:Medical University Graz; Department of Rheumatology and Immunology | ||
Full Title: Validation of the PsASon ULtrasound scores in patients with psoriatic arthritis undergoing TReatment with Apremilast | ||
Medical condition: Consecutive patients with PsA and with clinically active peripheral disease (arthritis, tenosynovitis, dactylitis and/or enthesitis) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2012-005723-33 | Sponsor Protocol Number: amantadineSCEDI. | Start Date*: 2015-03-27 |
Sponsor Name:GGZ Oost Brabant | ||
Full Title: Efficacy of amantadine on behavioural and emotional problems and impairment of executive functioning due to acquired brain injury to the frontal lobes: a series of single case experimental design s... | ||
Medical condition: behavioural and emotional problems and impairment of executive functioning due to acquired brain injury to the frontal lobes | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001539-23 | Sponsor Protocol Number: PET_ONKO | Start Date*: 2006-06-07 |
Sponsor Name:department of clinical pharmacology | ||
Full Title: Does imatinib therapy lead to an increased uptake of low molecular weight substances into solid tumor metastasis in patients with hormone refractory prostate cancer? | ||
Medical condition: patients with HRPC and bone metastases will be enrolled in the study | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-005026-31 | Sponsor Protocol Number: EFC6125 [AVE0005A/3001] | Start Date*: 2006-04-24 |
Sponsor Name:Sanofi-Synthelabo Recherche, a subsidiary of sanofi-aventis group | ||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Arm Study of the Effect of Intravenous AVE0005 (VEGF Trap) Administered Every 2 Weeks in Advanced Ovarian Cancer Patients with ... | ||
Medical condition: pacientes con cáncer de ovario avanzado con ascitis maligna sintomática recurrente | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Completed) GB (Completed) HU (Completed) AT (Prematurely Ended) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-007888-24 | Sponsor Protocol Number: 0881X1-4508-FR | Start Date*: 2008-07-31 |
Sponsor Name:Wyeth Pharmaceuticals France | ||
Full Title: Open-label Study to Evaluate the EULAR-RAID Score, Rheumatoid Arthritis Impact of Disease Score, in Rheumatoid Arthritis Patients Eligible to Etanercept and Who Will Receive Etanercept. | ||
Medical condition: RHEUMATOID ARTHRITIS | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-000815-42 | Sponsor Protocol Number: HighNxGHR_PK | Start Date*: 2015-04-28 | |||||||||||
Sponsor Name:Rigshospitalet, Copenhagen University Hospitals | |||||||||||||
Full Title: Pharmacokinetics of High-dose Target-controlled Naloxone Infusion. Companion study to: Effect of High-dose Target-controlled Naloxone Infusion on Pain and Hyperalgesia in Patients following Groin-H... | |||||||||||||
Medical condition: Healthy subjects | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002499-42 | Sponsor Protocol Number: Version1on02-02-2018 | Start Date*: 2018-08-29 |
Sponsor Name:Cliniques Universitaires Saint-Luc | ||
Full Title: Evaluation of the effect of repeated injections of high doses of botulinum toxin into the lower limb of spastic brain lesions on functional and biomechanical parameters of walking | ||
Medical condition: Patients with spastic brain lesions. Children with cerebral palsy (CP) and in the hemiplegic adult. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004579-37 | Sponsor Protocol Number: MZ12-PCP-PalenicekTomas-A | Start Date*: 2014-06-18 |
Sponsor Name:National Institute of Mental Health | ||
Full Title: Animal and human serotonergic model of schizophrenia: validity evaluated by qEEG and fMRI | ||
Medical condition: Inclusion criteria: a) Men and women at age between 28 and 65 years b) healthy volunteers with negative psychiatric history (severe mental illnesses that meet the criteria of ICD 10 F0.X - F99.X) ... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003821-25 | Sponsor Protocol Number: HIL-01 | Start Date*: 2005-10-11 |
Sponsor Name:Psychiatric Hospital | ||
Full Title: A 12 week multi-centre, randomized, double-blind, placebo controlled evaluation of the most efficacious and tolerable dose of escitalopram in the treatment of elderly patients. | ||
Medical condition: Depression in the elderly | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2020-000716-30 | Sponsor Protocol Number: RGL-003-001 | Start Date*: 2020-09-10 | |||||||||||
Sponsor Name:Gedeon Richter Plc. | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multicenter, proof-of-concept study to evaluate a combined oral contraceptive (COC) containing 30 µg ethinylestradiol and 150 µg levonorgestrel plus ... | |||||||||||||
Medical condition: Hypoactive sexual desire disorder (HSDD) secondary to combined oral contraception use. | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) BG (Completed) PL (Completed) CZ (Completed) RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020081-22 | Sponsor Protocol Number: R&D 2185 | Start Date*: 2011-02-08 |
Sponsor Name:North Bristol NHS Trust | ||
Full Title: The administration of Parathyroid hormone affects functional recovery from pertrochanteric fractured neck of femur: A prospective randomised comparative pilot study with blinded objective functiona... | ||
Medical condition: Osteoporotic or low energy pertrochanteric hip fractures | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003914-10 | Sponsor Protocol Number: sept2014 | Start Date*: 2015-02-02 |
Sponsor Name:uzleuven | ||
Full Title: ELABORATION OF A PATIENT-FRIENDLY TREATMENT STRATEGY WITH CAPSAICIN NASAL SPRAY IN PATIENTS WITH IDIOPATHIC RHINITIS | ||
Medical condition: idiopathic rhinitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-002687-14 | Sponsor Protocol Number: FUC 0301 INT | Start Date*: 2004-11-15 | |||||||||||
Sponsor Name:LEO Pharmaceutical Products Ltd. A/S (LEO Pharma A/S) | |||||||||||||
Full Title: Fucidin® Cream in the Treatment of Impetigo A phase IV study comparing clinical and bacteriological efficacy of Fucidin® cream with Fucidin® cream vehicle in the treatment of impetigo in paediatric... | |||||||||||||
Medical condition: Patients with a clinical diagnosis of impetigo, aged 2-11 years, with a severity score of minimum 1 for at least one of the following signs: Pustules/infected bullae, erythema and infiltration/indu... | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019647-19 | Sponsor Protocol Number: MAC_001 | Start Date*: 2011-02-04 |
Sponsor Name:University of Oxford | ||
Full Title: A double blind randomised placebo controlled trial of montelukast in the treatment of acute persistent cough in young people and adults (aged 16-49) in primary care | ||
Medical condition: Acute persistent cough with no established diagnosis | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-001801-42 | Sponsor Protocol Number: EPU-P76 | Start Date*: 2014-11-25 |
Sponsor Name:Maastricht University | ||
Full Title: Sensitivity of driving-related psychometric tests to the effects of two widely prescribed benzodiazepines: diazepam and oxazepam | ||
Medical condition: None | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003331-10 | Sponsor Protocol Number: HC03 | Start Date*: 2017-10-16 |
Sponsor Name:Leiden University | ||
Full Title: Acute effects of 40 mg cortisol on emotion and cognition. | ||
Medical condition: None. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-001453-23 | Sponsor Protocol Number: G-85974806 | Start Date*: 2023-01-12 |
Sponsor Name:ASATE | ||
Full Title: Pilot safety study of neoadjuvant radiotherapy in patients with glioblastoma. | ||
Medical condition: Glioblastoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-000393-20 | Sponsor Protocol Number: AX-CES1.2020 | Start Date*: 2020-10-23 | |||||||||||
Sponsor Name:DIP. MEDICINA DEI SISTEMI UNIVERSITà DEGLI STUDI DI ROMA TOR VERGATA | |||||||||||||
Full Title: USE OF SULFUR HEXAFLUORIDE MICROBUBBLES IN INTRAOPERATIVE SURGICAL EVALUATION OF AXILLARY LYMPH NODES IN LOCO-REGIONAL ANESTHESIA BREAST SURGERY: COMPARISON WITH THE TRADITIONAL METHODICAL. PRELIMI... | |||||||||||||
Medical condition: Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000432-27 | Sponsor Protocol Number: 5/2006/O/Sper | Start Date*: 2006-03-16 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Epidural analgesia vs systemic intravenous analgesia in the major gynecological surgery | |||||||||||||
Medical condition: increased isteroannessiectomia, isteroannessiectomia with linfoadenectomia, annessiectomia with linfoadenectomia with omentectomia, removal focus of endometriosis 4 stage | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002545-42 | Sponsor Protocol Number: INS-415 | Start Date*: 2021-02-08 | |||||||||||
Sponsor Name:Insmed Incorporated | |||||||||||||
Full Title: ARISE - A Randomized, Double-Blind, Placebo-Controlled, Active Comparator, Multicenter Study to Validate Patient-Reported Outcome Instruments in Adult Subjects with Newly Diagnosed Nontuberculous M... | |||||||||||||
Medical condition: Adult Subjects with Newly Diagnosed Nontuberculous Mycobacterial (NTM) Lung Infection Caused by Mycobacterium avium Complex (MAC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) DE (Completed) HU (Completed) AT (Completed) NL (Completed) GR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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