- Trials with a EudraCT protocol (717)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (73)
717 result(s) found for: Diagnostic tests.
Displaying page 1 of 36.
EudraCT Number: 2018-004159-19 | Sponsor Protocol Number: 2018-00938 | Start Date*: Information not available in EudraCT |
Sponsor Name:University Hospital Basel | ||
Full Title: Use of Copeptin Measurement after Arginine Infusion for the Diagnosis of Diabetes Insipidus - the CARGOx Study | ||
Medical condition: Polyuria-polydipsia syndrome (PPS) is divided into the three main entities central (complete or partial) diabetes insipidus (DI), nephrogenic DI and primary polydipsia (PP). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004397-99 | Sponsor Protocol Number: MBCC28040 | Start Date*: 2014-06-17 |
Sponsor Name:Instituto Tecnológico PET, S.A.U. (ITP) | ||
Full Title: A Phase III Clinical Trial to evidence the safety and efficacy of the radio-drug 18f-Fluorocholine (18F-FCH), using Positron Emission Tomography (PET) for the diagnosis of the prostate carcinoma in... | ||
Medical condition: Prostate Carcinoma in patients with biochemical relapse. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-023095-31 | Sponsor Protocol Number: HUM-001 | Start Date*: 2012-11-28 | |||||||||||
Sponsor Name:Humedics GmbH | |||||||||||||
Full Title: | |||||||||||||
Medical condition: liver resection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000824-36 | Sponsor Protocol Number: HLSC-UCD-01 | Start Date*: 2021-12-09 | |||||||||||
Sponsor Name:Unicyte AG | |||||||||||||
Full Title: An open-label, controlled, multi-site, Phase I clinical trial to assess the ureagenesis capacity in newborns and infants up to the age of 12 months with neonatal and infantile onset of urea cycle d... | |||||||||||||
Medical condition: Subject has a genetically confirmed diagnosis of any of the following urea cycle disorders: ASS, CPS1, ASL, OTC Subjects without UCD can have other stable illness that not interfere with the clini... | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) AT (Prematurely Ended) IT (Prematurely Ended) BE (Completed) DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007405-37 | Sponsor Protocol Number: 1497/08 | Start Date*: 2009-03-07 | ||||||||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | ||||||||||||||||||
Full Title: Multicenter, not-for-profit study to evaluate tolerability, safety of tramadol once-a-day in older patients with dementia and difficulty to verbalize | ||||||||||||||||||
Medical condition: Pain in older patients with dementia | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003958-25 | Sponsor Protocol Number: PI18/01097 | Start Date*: 2019-10-25 |
Sponsor Name:Fundación Pública Andaluza para la Gestión de la Investigación en Salud de Sevilla | ||
Full Title: Screening for cancer with PET / CT in patients with unprovoked venous thromboembolic disease with a high risk of developing cancer. Open randomized clinical trial. | ||
Medical condition: Venous thromboembolic disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002597-41 | Sponsor Protocol Number: O321 | Start Date*: 2018-11-14 | |||||||||||
Sponsor Name:Adamed Pharma S.A. | |||||||||||||
Full Title: A multi-centre clinical trial evaluating patients’ ability to independently and safely use the medicinal product indicated in the treatment of erectile dysfunction | |||||||||||||
Medical condition: Erectile dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002527-21 | Sponsor Protocol Number: AMYPAD-01 | Start Date*: 2018-05-23 |
Sponsor Name:University of Geneva | ||
Full Title: Multicentre, Open-label, Randomised Study to Assess the Diagnostic Value of Amyloid PET Imaging in Patients with Subjective Cognitive Decline Plus, Mild Cognitive Impairment, or Dementia Where Alzh... | ||
Medical condition: Alzheimer's disease Mild Cognitive Impairment Subjective Cognitive Decline Plus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) DE (Completed) ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-001158-41 | Sponsor Protocol Number: P.64CU.001.01 | Start Date*: 2016-02-19 | |||||||||||
Sponsor Name:SPARKLE SRL | |||||||||||||
Full Title: “Technical and diagnostic performances of PET/CT with 64Cu(II)Cl2 in localization of metastases from prostate carcinoma, in patients undergoing restaging for disease progression during ADT” | |||||||||||||
Medical condition: metastatic prostate carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000274-36 | Sponsor Protocol Number: APACH2 | Start Date*: 2019-07-03 | |||||||||||
Sponsor Name:Centre François Baclesse | |||||||||||||
Full Title: Phase III trial comparing 2 diagnostic strategies for the preoperative localization of parathyroid adenoma in primary hyperparathyroidism: TEMP / CT with Tc99m-sestaMIBI or PET / CT with F18-choli... | |||||||||||||
Medical condition: Patient with primary hyperparathyroidism and for which surgical resection is provided. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000316-31 | Sponsor Protocol Number: HIDR-0721/COV | Start Date*: 2021-07-15 |
Sponsor Name:FAES FARMA S.A. | ||
Full Title: Multicenter, double-blind, randomized clinical trial to evaluate the efficacy of calcifediol soft capsules versus placebo in reducing hospital admissions in patients with a positive diagnostic test... | ||
Medical condition: SARS-CoV-2 coronavirus infection (COVID-19). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-000210-21 | Sponsor Protocol Number: TON/02/05-CLIN | Start Date*: 2006-03-27 |
Sponsor Name:Prof Jes Olesen | ||
Full Title: A single centre, double-blind, randomised, placebo controlled cross-over study to evaluate the efficacy and tolerability of tonabersat in the prophylaxis of migraine in patients presenting with mig... | ||
Medical condition: Migraine with aura meeting the diagnostic criteria of the International Classification of Headache Disorders (Edition 2) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-006561-32 | Sponsor Protocol Number: OxyCog-01 | Start Date*: 2009-11-05 |
Sponsor Name:LWL University Hospital Bochum | ||
Full Title: Effects of intranasal application of oxytocin on empathy and mentalising in patients with psychotic disorders and severe personality disorders | ||
Medical condition: Schizophrenia, bipolar disorder, major depression, personality disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-002592-34 | Sponsor Protocol Number: RID-TB:Dx | Start Date*: 2020-08-28 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: Research to Improve the Detection and Treatment of Latent Tuberculosis Infection: Diagnostics (RID-TB:Dx) A randomised controlled trial to evaluate the effectiveness of using the RD-1 based C Tb s... | |||||||||||||
Medical condition: Latent Tuberculosis infection (LTBI) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001342-28 | Sponsor Protocol Number: PHRC2013-02 | Start Date*: 2015-07-23 |
Sponsor Name:CHU Angers | ||
Full Title: TOMOSCINTIGRAPHIE HYBRIDE AUX LEUCOCYTES MARQUES DANS LE DIAGNOSTIC DES INFECTIONS DE PROTHESES VASCULAIRES. Etude LEUCOPRO® | ||
Medical condition: infection de prothèse vasculaire | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-005169-39 | Sponsor Protocol Number: D9914C00002 | Start Date*: 2005-08-11 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A single-blind single arm study to validate the Reflux Disease Questionnaire (RDQ) for the diagnosis of reflux disease in primary care in patients treated with esomeprazole 40 mg o.d. | ||
Medical condition: Symptoms from the upper gastrointestinal tract | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) GB (Completed) DE (Completed) DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-004979-19 | Sponsor Protocol Number: EK Reg.-Nr. 040-2007 | Start Date*: 2009-01-08 |
Sponsor Name:University of Leipzig | ||
Full Title: In-vivo assessment of nicotinic acetylcholine receptor binding in neurodegenerative diseases using the radioligand 2-[18F]FA-85380 and positron emission tomography (PET) | ||
Medical condition: To test a diagnostic imaging tool for specifically assessing the nicotinic acetylcholine receptor in vivo in patients with neurodegenerative diseases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-003652-21 | Sponsor Protocol Number: 2019-23 | Start Date*: 2020-01-23 | |||||||||||
Sponsor Name:OSPEDALE CLASSIFICATO EQUIPARATO SACRO CUORE DON CALABRIA - PRESIDIO OSPEDALIERO ACCREDITATO | |||||||||||||
Full Title: Interventional two arms open-label study for evaluating the diagnostic performance of PET PSMA in patients affected by biochemical recurrent prostate cancer. | |||||||||||||
Medical condition: Biochemical recurrent prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003956-30 | Sponsor Protocol Number: CHDR1429 | Start Date*: 2014-10-13 |
Sponsor Name:Centre for Human Drug Research | ||
Full Title: A single-centre randomized double-blind, double-dummy, placebo-controlled, four-way crossover study in healthy subjects to investigate the effect of ethanol 0.5 and 1.0 g/L and alprazolam 1 mg on a... | ||
Medical condition: A total of 24 healthy subjects, both male and female, will be enrolled into the study following satisfactory completion of a screening visit where eligibility for the study will be checked. Subje... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002534-37 | Sponsor Protocol Number: RAME-04 | Start Date*: 2021-03-08 | |||||||||||
Sponsor Name:ENTE OSPEDALIERO OSPEDALI GALLIERA | |||||||||||||
Full Title: Diagnostic and predictive role of 64CuCl2 PET / CT in bladder cancer patients eligible for chemotherapy | |||||||||||||
Medical condition: bladder cancer patients eligible for cisplatin chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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