- Trials with a EudraCT protocol (14)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
14 result(s) found for: Digital medicine.
Displaying page 1 of 1.
EudraCT Number: 2017-000317-22 | Sponsor Protocol Number: BRE-ASA01 | Start Date*: 2017-04-13 |
Sponsor Name:Linköping University | ||
Full Title: A pilot study of low dose acetylsalicylic acid (ASA) for reduction of breast density and inflammation | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002494-10 | Sponsor Protocol Number: | Start Date*: 2020-07-17 | |||||||||||
Sponsor Name:Queen Mary University of London | |||||||||||||
Full Title: Personalised Electronic Record Supported OptimisatioN when ALone for Patients with Hypertension- Pilot Study for Remote Medical Management of Hypertension During the COVID-19 Pandemic | |||||||||||||
Medical condition: Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004602-17 | Sponsor Protocol Number: 031-201-00186 | Start Date*: 2018-03-12 | |||||||||||
Sponsor Name:Otsuka Pharmaceutical | |||||||||||||
Full Title: A Multicentre, 8-week, Single-arm, Open-label, Pragmatic Trial to Explore Acceptance and Performance of Using a Digital Medicine System with Healthcare Professionals and Adult Subjects with Schizo... | |||||||||||||
Medical condition: Schizophrenia, Schizoaffective Disorder, or First Episode Psychosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000531-17 | Sponsor Protocol Number: D5160C00002 | Start Date*: 2014-05-20 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase II, Open Label, Single-arm Study to Assess the Safety and Efficacy of AZD9291 in Patients with EGFRm+/T790M+, Locally Advanced or Metastatic NSCLC who have Progressed Following Prior Therap... | |||||||||||||
Medical condition: Non Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001387-28 | Sponsor Protocol Number: NL73559.091.20 | Start Date*: 2020-06-22 | ||||||||||||||||
Sponsor Name:Radboud University Medical Center | ||||||||||||||||||
Full Title: 18F-PSMA-1007 PET to detect primary prostate cancer: a comparative study with mpMRI and correlation to histopathology. | ||||||||||||||||||
Medical condition: 75 patients with the suspicion on PCa (elevated PSA and/or abnormal digital rectal exam) will receive a PSMA-PET following mpMRI. 25 patients with PIRADS 1-2 (probably benign disease), 25 patients ... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000123-12 | Sponsor Protocol Number: 2020110469 | Start Date*: 2021-06-22 |
Sponsor Name:Odense University Hospital | ||
Full Title: PRISMA-PET – Primary Staging of Prostate Cancer: A Randomized Controlled Trial Comparing 18F-PSMA-1007 PET/CT to Conventional Imaging. | ||
Medical condition: Newly diagnosed prostate cancer, PET/CT scan used to stage newly diagnosed prostate cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003391-40 | Sponsor Protocol Number: 2020-KEP-456 | Start Date*: 2020-12-17 | |||||||||||
Sponsor Name:London School of Hygiene and Tropical Medicine | |||||||||||||
Full Title: Intramuscular tranexamic acid for the treatment of symptomatic mild traumatic brain injury in older adults: a randomised, double-blind, placebo-controlled trial. | |||||||||||||
Medical condition: Mild traumatic brain injury. | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002276-37 | Sponsor Protocol Number: AK-2017-PC-1 | Start Date*: 2017-08-25 | |||||||||||
Sponsor Name:Rigshospitalet, Department of Clinical Physiology, Nuclear Medicine & PET | |||||||||||||
Full Title: Phase II trial: uPAR-PET/MR in patients with newly diagnosed prostate cancer; non-invasive characterization of tumor aggressiveness | |||||||||||||
Medical condition: Prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000580-24 | Sponsor Protocol Number: | Start Date*: 2019-05-17 |
Sponsor Name:Hull & East Yorkshire Hospitals NHS trust | ||
Full Title: A single arm, open-label clinical trial of azithromycin in pulmonary sarcoidosis | ||
Medical condition: Sarcoidosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2019-000245-12 | Sponsor Protocol Number: Repha_1436 | Start Date*: 2020-01-20 | ||||||||||||||||
Sponsor Name:Repha GmbH | ||||||||||||||||||
Full Title: Controlled clinical trial to evaluate the efficacy and safety of MYRRHINIL-INTEST® versus placebo in patients with diarrhea-dominant irritable bowel syndrome (IBS-D) and patients with mixed-type ir... | ||||||||||||||||||
Medical condition: A confirmed diagnosis of irritable bowel syndrome (IBS-D or IBS-M) by a specialist in gastroenterology and/or internal medicine and/or general medicine | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001464-19 | Sponsor Protocol Number: GE-122-020 | Start Date*: 2016-02-11 | ||||||||||||||||
Sponsor Name:GE Healthcare Ltd. and its affiliates | ||||||||||||||||||
Full Title: AdreView™ Myocardial Imaging for Risk Evaluation – A multicentre trial to guide ICD implantation in NYHA class II & III heart failure patients with 30%≤LVEF≤35% ADMIRE-ICD | ||||||||||||||||||
Medical condition: Heart failure | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Prematurely Ended) ES (Prematurely Ended) NL (Prematurely Ended) CZ (Prematurely Ended) DE (Prematurely Ended) DK (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-005823-35 | Sponsor Protocol Number: 20201206 | Start Date*: 2021-01-28 | |||||||||||||||||||||
Sponsor Name:Aarhus Universitet [...] | |||||||||||||||||||||||
Full Title: ILIT.FT – Dose finding for intralymphatic allergen immunotherapy in a randomized, parallel group, double blind placebo-controlled field trial | |||||||||||||||||||||||
Medical condition: Allergic rhinitis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002749-37 | Sponsor Protocol Number: ISAV | Start Date*: 2011-10-11 | |||||||||||
Sponsor Name:UNIVERSITA' DEGLI STUDI DI MILANO - BICOCCA | |||||||||||||
Full Title: Validation of digital-PCR analysis through programmed imatinib interruption in PCR negative chronic myeloid leukemia patients. | |||||||||||||
Medical condition: Chronic Myeloid Leukemia (CML) with substained Complete Molecular Response (CMR). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) ES (Completed) DE (Completed) NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001060-28 | Sponsor Protocol Number: 2020-001060-28 | Start Date*: 2021-03-16 | |||||||||||||||||||||
Sponsor Name:Aarhus Universitet | |||||||||||||||||||||||
Full Title: Documentation of efficacy for intralymphatic allergen immunotherapy in a phase III randomized, parallel group, double blind placebo-controlled multisite field trial | |||||||||||||||||||||||
Medical condition: Allergic rhinitis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) SE (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
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