- Trials with a EudraCT protocol (134)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
134 result(s) found for: Intention to treat analysis.
Displaying page 1 of 7.
EudraCT Number: 2017-005179-21 | Sponsor Protocol Number: 4RIBC-2018 | Start Date*: 2018-03-09 | |||||||||||
Sponsor Name:Department of infectious Diseases, Odense University Hospital | |||||||||||||
Full Title: Four weeks treatment for chronic hepatitis C in patients under 50 years of age with no significant liver fibrosis | |||||||||||||
Medical condition: Chronic Hepatitis C | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003139-31 | Sponsor Protocol Number: 38RC18.103 | Start Date*: 2018-12-04 |
Sponsor Name:CHU GRENOBLE ALPES | ||
Full Title: Efficacy and safety of levocetirizine alone or in combination with tranexamic acid in the treatment of spontaneous chronic urticaria. Multicentric controlled randomized study in cross-over, double-... | ||
Medical condition: Chronique Spontaneous urticaria | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000151-10 | Sponsor Protocol Number: TAR-PRO | Start Date*: 2017-08-02 |
Sponsor Name:Fundación para la Investigación Biomédica del Hospital Universitario La Paz | ||
Full Title: Antiretroviral therapy proviral genotype-guided: pilot-proof of concept clinical trial. | ||
Medical condition: Human Immunodeficiency Virus | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002977-44 | Sponsor Protocol Number: ASAA-Study | Start Date*: 2011-06-28 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA "OSPEDALI RIUNITI DI BERGAMO" (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: Antibiotics vs Surgery in Acute Appendicitis: an intention to treat prospective randomised controlled study, The ASAA-Study | |||||||||||||
Medical condition: All the patients between 18 and 65 years old admitted to the hospital with a first episode of suspected acute appendicitis diagnosed by Andersson's score | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001554-61 | Sponsor Protocol Number: ACASA-TAVI-2.1 | Start Date*: 2021-08-19 |
Sponsor Name:Oslo University Hospital | ||
Full Title: Anti-Coagulation versus AcetylSalicylic Acid after Transcatheter Aortic Valve Implantation (ACASA-TAVI) | ||
Medical condition: Patients with aortic stenosis undergoing transcatheter aortic valve implantation. | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NO (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001617-32 | Sponsor Protocol Number: MINOR | Start Date*: 2013-12-05 |
Sponsor Name:AUSL di Piacenza | ||
Full Title: Thrombolysis in Minor Stroke | ||
Medical condition: The condition to be treated is the stroke of “minor” grade (National Institutes of Health Stroke Scale (NIHSS) score < 5). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001060-21 | Sponsor Protocol Number: 374/11 | Start Date*: 2011-10-17 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Safety and efficacy of switching a stable combined antiretroviral therapeutic regimen to atazanavir with ritonavir plus lamivudine in treatment experienced HIV positive patients with full and stabl... | |||||||||||||
Medical condition: HIV | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002378-68 | Sponsor Protocol Number: SIRES | Start Date*: 2007-10-30 | |||||||||||
Sponsor Name:SERVICIO NEFROLOGIA HOSPITAL BELLVITGE | |||||||||||||
Full Title: Estudio piloto de Selección de la Inmunosupresión basado en un régimen basado en inhibidores de CNI o libre de CNI dependiendo de la aloreactividad donante-especifica mediante el ensayo ELISPOT en ... | |||||||||||||
Medical condition: PATIENTS THAT RECEIVE A FIRST RENAL ALLOGRAFT TRANSPLANTATION. It has been shown that the assessment of the donor specific T-cell alloimmune response can be successfully performed by using new too... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006041-36 | Sponsor Protocol Number: PH-L19IL2TNFBASK-04/21 | Start Date*: 2022-02-08 |
Sponsor Name:Philogen S.p.A. | ||
Full Title: A phase II study of L19IL2/L19TNF in patients with skin cancers amenable to intralesional treatment | ||
Medical condition: Patients with malignant tumors of the skin amenable to intratumoral injection, and in a curative or neoadjuvant or palliative intention, including: • Basal cell carcinoma (BCC) • Cutaneous squamou... | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) IT (Trial now transitioned) ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004436-19 | Sponsor Protocol Number: Tribe-2 | Start Date*: 2014-12-22 |
Sponsor Name:G.O.N.O. | ||
Full Title: First-line FOLFOXIRI plus bevacizumab followed by reintroduction of FOLFOXIRI plus bevacizumab at progression versus FOLFOX plus bevacizumab followed by FOLFIRI plus bevacizumab at progression in f... | ||
Medical condition: METASTATIC COLORECTAL CANCER | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000515-14 | Sponsor Protocol Number: GESIDA8014 | Start Date*: 2014-06-26 | |||||||||||
Sponsor Name:Fundación SEIMC-GESIDA | |||||||||||||
Full Title: Comparative, randomized, open study to evaluate maintenance with Darunavir/ritonavir once daily plus Lamivudine once daily versus continuing Darunavir/ritonavir once-daily plus Tenofovir/Emtricitab... | |||||||||||||
Medical condition: HIV chronic infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001121-24 | Sponsor Protocol Number: P00804 | Start Date*: 2011-04-21 |
Sponsor Name:Papworth Hospital NHS Trust | ||
Full Title: Prospective randomised controlled trial of video assisted thorascopic (VATS) cytoreductive pleurectomy compared to talc pleurodesis in patients with suspected or proven malignant mesothelioma | ||
Medical condition: Mesothelioma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004354-28 | Sponsor Protocol Number: S-20120017 | Start Date*: 2013-07-02 |
Sponsor Name:Børneafdelingen Kolding | ||
Full Title: Maintenance treatment in childhood constipation. A randomized placebo-controlled intervention study | ||
Medical condition: Childhood functional constipation. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-002852-17 | Sponsor Protocol Number: GOG-0277 | Start Date*: 2013-03-13 | |||||||||||
Sponsor Name:EORTC | |||||||||||||
Full Title: A Phase III Randomised Trial of Gemcitabine plus Docetaxel followed by Doxorubicin versus observation for uterus-limited, high grade uterine leiomyosarcoma | |||||||||||||
Medical condition: Patients with high risk uterine LMS, FIGO stage I (confined to corpus +/- cervix). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) FR (Prematurely Ended) BE (Prematurely Ended) ES (Prematurely Ended) NL (Prematurely Ended) DE (Prematurely Ended) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000256-35 | Sponsor Protocol Number: CNPOBC2020 | Start Date*: 2020-12-16 | |||||||||||
Sponsor Name:Aalborg University Hospital | |||||||||||||
Full Title: Intravenous immunoglobulin and prednisolone to women with unexplained recurrent pregnancy loss after assisted reproductive technology treatment: a randomised, double-blind, placebo-controlled trial | |||||||||||||
Medical condition: Recurrent pregnancy loss after assisted reproductive technology treatment | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005589-31 | Sponsor Protocol Number: 44-2015 | Start Date*: 2015-03-25 | |||||||||||
Sponsor Name:Department of infectious Diseases, Odense University Hospital | |||||||||||||
Full Title: 4 Week treatment for Injecting Drug Users with chronic hepatitis C A phase 4, post marketing randomized clinical open label trial comparing 4 weeks of Ledipasvir/Sofosbuvir (co-formulated) and Ri... | |||||||||||||
Medical condition: Chronic Hepatitis C in patients with no or minimal liver fibrosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-005066-22 | Sponsor Protocol Number: CTSU_MDCO-PCS-17-01 | Start Date*: 2018-06-11 | |||||||||||
Sponsor Name:University of Oxford [...] | |||||||||||||
Full Title: HPS-4/TIMI 65/ORION-4: A double-blind randomized placebo-controlled trial assessing the effects of inclisiran on clinical outcomes among people with atherosclerotic cardiovascular disease | |||||||||||||
Medical condition: Atherosclerotic cardiovascular disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005569-12 | Sponsor Protocol Number: CSTI571E2203 | Start Date*: 2006-01-26 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A randomized, double-blind, placebo-controlled study to evaluate the safety and efficacy of six months treatment with the tyrosine kinase inhibitor of STI571 for the treatment of pulmonary arterial... | ||
Medical condition: pulmonary arterial hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Prematurely Ended) AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-002947-74 | Sponsor Protocol Number: 1-12 | Start Date*: 2013-07-19 |
Sponsor Name:Medizinische Universität Wien | ||
Full Title: A prospective randomized, double blind, placebo-controlled, cross-over study to investigate the analgesic effect of Aspirin® to prevent the pain during the treatment with capsaicin patch 8% (Qutenza®) | ||
Medical condition: Qutenza is an approved product for the treatment of pain due to postherpetic neuralgia and peripheral neuropathies. Since its application is painful, it is often necessary to give analgesics or loc... | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-000671-25 | Sponsor Protocol Number: 1242-001 | Start Date*: 2016-09-30 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Randomized Parallel-Group, Placebo-Controlled, Double-Blind, Event-Driven, Multi- Center Pivotal Phase III Clinical Outcome Trial of Efficacy and Safety of the Oral sGC Stimulator Vericiguat in S... | |||||||||||||
Medical condition: Treatment of chronic heart failure with reduced ejection fraction (HFrEF) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) CZ (Completed) HU (Completed) ES (Completed) FR (Completed) GB (Completed) DK (Completed) NL (Completed) FI (Completed) PL (Completed) BE (Completed) GR (Completed) AT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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