- Trials with a EudraCT protocol (620)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
620 result(s) found for: Effect size.
Displaying page 1 of 31.
EudraCT Number: 2013-005430-37 | Sponsor Protocol Number: | Start Date*: 2015-01-02 | |||||||||||
Sponsor Name:North Bristol NHS Trust | |||||||||||||
Full Title: Use of co-trimoxazole to prevent pneumonia in patients with severe head injury | |||||||||||||
Medical condition: Pneumonia secondary to severe head injury. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003686-13 | Sponsor Protocol Number: P04805-V2.0 | Start Date*: 2007-05-31 | ||||||||||||||||
Sponsor Name:Allergie-Centrum-Charite, Department of Dermatology, Charite - Universitätsmedizin Berlin | ||||||||||||||||||
Full Title: An exploratory phase III, randomised, double blind, therapeutic single dose-related effect, parallel group study to assess and compare the effects of 5mg vs. 20mg Desloratadine on skin lesions in p... | ||||||||||||||||||
Medical condition: Chronic urticaria is characterized by the spontaneous development of wheal and flare type skin reactions. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-002724-17 | Sponsor Protocol Number: 02-NDOL-006 | Start Date*: 2005-04-19 |
Sponsor Name:Fresenius Kabi Deutschland GmbH | ||
Full Title: Efficacy of Neodolpasse™ in the treatment of postoperative pain: Morphine sparing effect during the first 24 hours postoperatively after unilateral total hip arthroplasty. | ||
Medical condition: Patients with ASA classification I-III, female or male between 18 and 85 years of age, undergoing primary cementless unilateral total hip arthroplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-000240-30 | Sponsor Protocol Number: 80308 | Start Date*: 2022-04-19 |
Sponsor Name:Center for Experimental and Molecular Medicine, G2 (AMC) | ||
Full Title: The chemopreventive effect of Lithium on adenoma development in patients with familial adenomatous polyposis (FAP); a pilot study | ||
Medical condition: Familial adenomatous polyposis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-001529-27 | Sponsor Protocol Number: 20050401 | Start Date*: 2005-06-13 |
Sponsor Name:Jan Engvall | ||
Full Title: Effect of reperfusion on infarct size and cardiac function evaluated with MRI and echocardiography/Effekt av reperfusion på infarktstorlek och hjärtfunktion utvärderat med MR och ultraljud | ||
Medical condition: Patients recovering 6weeks after primary PCI for ST-elevation Myocardial Infarction. This application concerns the use of gadolinium contrast to visualise myocardial infarct size using MRI. Aden... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000349-30 | Sponsor Protocol Number: NL60669 | Start Date*: 2017-08-02 |
Sponsor Name:Academic Medical Center | ||
Full Title: Effect of INtervention with DMR, GLP-1 and lifestyle intensification -in Subjects with insulin dePendent type 2 diabetes- on Insulin Requirement and mEtabolic parameters | ||
Medical condition: Type 2 diabetes mellitus | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-005226-19 | Sponsor Protocol Number: SitaDFU_v1.0 | Start Date*: 2016-07-19 |
Sponsor Name:Medical University of Innsbruck | ||
Full Title: Accelerated wound healing in diabetic ulcers by Sitagliptin | ||
Medical condition: diabetic foot ulcer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-003671-30 | Sponsor Protocol Number: VHL-HOPE-2014-1 | Start Date*: 2014-10-31 |
Sponsor Name:ALIANZA ESPAÑOLA DE FAMILIAS DE VON HIPPEL-LINDAU | ||
Full Title: Therapeutic effect of propranolol in a series of patients with von Hippel-Lindau disease and retinal hemangioblastomas in short, medium and long term treatment. | ||
Medical condition: VON HIPPEL-LINDAU DISEASE | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004291-21 | Sponsor Protocol Number: 33IC30_166855 | Start Date*: 2018-01-15 |
Sponsor Name:Insel Gruppe AG - Inselspital Universitätsklinik für Kardiologie | ||
Full Title: Effect of phosphodiesterase-5 inhibition with Tadalafil on SystEmic Right VEntricular size and function – a multi-center, double-blind, randomized, placebo-controlled clinical trial – SERVE Trial | ||
Medical condition: Adults with congenital heart disease (CHD) and a right ventricle (RV) in subaortic (systemic) position. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-004505-34 | Sponsor Protocol Number: 201800881 | Start Date*: 2021-02-17 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: A phase 2a study on the anti-tumoral effect of cannabis oil (THC 10% / CBD 5%) in patients with advanced untreatable hepatocellular carcinoma | ||
Medical condition: The anti-tumoral effect of cannabis oil will be investigated in patients with untreatable HCC | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003415-22 | Sponsor Protocol Number: AP-W-CLI-2018-8 | Start Date*: 2019-03-22 | |||||||||||
Sponsor Name:Aurealis Oy | |||||||||||||
Full Title: A Phase 1/2A clinical study to evaluate the safety, tolerability and efficacy of single and repeated doses of AUP1602-C as topical treatment of diabetic foot ulcers | |||||||||||||
Medical condition: Diabetic foot ulcers | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001234-22 | Sponsor Protocol Number: NL52821.018.15 | Start Date*: 2015-07-01 | |||||||||||
Sponsor Name:Academic Medical Center | |||||||||||||
Full Title: A randomized placebo-controlled study in patients with a Gallium-68 DOTATATE PET/CT positive, clinically non-functioning pituitary macroadenoma (NFMA) of the effect of Lanreotide autosolution on Tu... | |||||||||||||
Medical condition: Clinically non-functioning pituitary macroadenoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000573-72 | Sponsor Protocol Number: ATOS-010 | Start Date*: 2018-04-21 |
Sponsor Name:Atossa Genetics Inc | ||
Full Title: Karma CREME-1: A double-blind, placebo-controlled, three-armed, pilot study of the effects, safety and tolerability of topical endoxifen in women within the Karma Cohort | ||
Medical condition: The mammographic density reduction in healthy women. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-001772-20 | Sponsor Protocol Number: CMR001/05 | Start Date*: 2007-03-15 |
Sponsor Name:Clinica Rotger | ||
Full Title: Effect of intracoronary injection of autologous stemm cells on left ventricular ejection fraction and volumes one year after an acute myocardial infarction. Efecto de la inyección intracoronaria d... | ||
Medical condition: The trial evaluates the effect on left ventricular function recovery of the intracoronary injection of mononuclear white cells obtained from peripheral blood in the week after an acute myocardial i... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003099-39 | Sponsor Protocol Number: LWH0604 | Start Date*: 2008-08-21 |
Sponsor Name:Liverpool Women's NHS Foundation Trust Hospital | ||
Full Title: A Randomised Controlled Trial of Thyroxine in Preterm Infants Under 28 weeks' Gestation. | ||
Medical condition: Hypothyroidism is a condition where there is a lack of thyroid hormone in the body. Thyroid hormones are important for normal brain development and growth. Children who are born with low thyroid ho... | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-002196-15 | Sponsor Protocol Number: DSC127-2012-02 | Start Date*: 2015-07-29 |
Sponsor Name:Derma Sciencs Inc | ||
Full Title: A Randomized, Double-Blind, Parallel-group, Vehicle and Standard of Care-controlled Phase 3 Clinical Trial to Evaluate the Efficacy and Safety of Aclerastide (DSC127) in Treating Non-healing Foot U... | ||
Medical condition: Diabetic Foot Ulcers | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: LV (Prematurely Ended) EE (Prematurely Ended) HU (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2022-002611-29 | Sponsor Protocol Number: 82050 | Start Date*: 2023-06-12 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: DEnosumab for the treatment of FIbrous Dysplasia/McCune-Albright Syndrome in adults (DeFiD): a randomized double-blind placebo-controlled trial | ||
Medical condition: Fibrous Dysplasia/ McCune Albright Syndrome | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-005046-12 | Sponsor Protocol Number: Final protocol | Start Date*: 2005-09-22 |
Sponsor Name:Ulster Community & Hospitals Trust | ||
Full Title: A double blind prospective randomised controlled trial to evaluate the effect of topical phenytoin on the healing of venous leg ulcers | ||
Medical condition: Venous Leg Ulceration | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002514-23 | Sponsor Protocol Number: Car20130917 | Start Date*: 2015-01-07 |
Sponsor Name:VU Medical Center | ||
Full Title: Reduction Of Microvascular Injury Utilizing Sonolysis | ||
Medical condition: Myocardial infarction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-000827-11 | Sponsor Protocol Number: T50/2021 | Start Date*: 2022-09-02 |
Sponsor Name:Turku University Hospital | ||
Full Title: Clinical use of USPIO contrast media in the assessment of pelvic lymph node metastasis in rectal cancer. | ||
Medical condition: Pelvic lymph node metastasis in rectal cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Trial now transitioned) | ||
Trial results: (No results available) |
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