Flag of the European Union EU Clinical Trials Register Help

Clinical trials for Conscience

The European Union Clinical Trials Register   allows you to search for protocol and results information on:
  • interventional clinical trials that were approved in the European Union (EU)/European Economic Area (EEA) under the Clinical Trials Directive 2001/20/EC
  • clinical trials conducted outside the EU/EEA that are linked to European paediatric-medicine development

    • EU/EEA interventional clinical trials approved under or transitioned to the Clinical Trial Regulation 536/2014 are publicly accessible through the
    Clinical Trials Information System (CTIS).

    The EU Clinical Trials Register currently displays   44338   clinical trials with a EudraCT protocol, of which   7368   are clinical trials conducted with subjects less than 18 years old.   The register also displays information on   18700   older paediatric trials (in scope of Article 45 of the Paediatric Regulation (EC) No 1901/2006).

    Phase 1 trials conducted solely on adults and that are not part of an agreed paediatric investigation plan (PIP) are not publicly available (see Frequently Asked Questions ).  
     
    Examples: Cancer AND drug name. Pneumonia AND sponsor name.
    How to search [pdf]
    Search Tips: Under advanced search you can use filters for Country, Age Group, Gender, Trial Phase, Trial Status, Date Range, Rare Diseases and Orphan Designation. For these items you should use the filters and not add them to your search terms in the text field.
    Advanced Search: Search tools
     
    28 result(s) found for: Conscience. Displaying page 2 of 2.
    « Previous 1  2 
    EudraCT Number: 2007-002319-16 Sponsor Protocol Number: Pr LEVY - PCa - CPRC 2006 Start Date*: 2007-09-07
    Sponsor Name:Centre Hospitalier Universitaire de Nancy
    Full Title: Modulation de la vasoréactivité dans le choc septique : impact de la protéine C recombinante
    Medical condition: sepsis : sont inclus les patients répondant aux critères conventionnels du choc septique qui intègrent ceux d’infection et d’infection sévère
    Disease: Version SOC Term Classification Code Term Level
    9.1 10040047 Sepsis LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: FR (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2021-004160-94 Sponsor Protocol Number: 69HCL21_0855 Start Date*: 2022-03-16
    Sponsor Name:HOSPICES CIVILS DE LYON
    Full Title: Etude de preuve de concept de phase IIB, multicentrique, en double aveugle, randomisée, contrôlée versus placebo, évaluant le diltiazem en association avec le traitement standard dans la prise en ...
    Medical condition: Patients adultes dont l’infection COVID-19 est confirmée par une RT-PCR, positive pour SARS-CoV-2, dans les 72h qui précèdent l’inclusion dans l’étude et nécessitant une hospitalisation en service ...
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: FR (Prematurely Ended)
    Trial results: View results
    EudraCT Number: 2014-000791-26 Sponsor Protocol Number: PHRI13-GF/LEVNEONAT-1 Start Date*: Information not available in EudraCT
    Sponsor Name:CHRU TOURS
    Full Title: Lévétiracétam pour le traitement en première intention des convulsions du nouveau-né : étude de phase II
    Medical condition: Nouveau-nés à terme présentant des convulsions dans les premières 72h de vie. Nés dans un contexte d'asphyxie périnatale qu'ils soient éligibles ou non à l'hypothermie thérapeutique.
    Disease: Version SOC Term Classification Code Term Level
    19.0 100000004852 10070512 Hypoxic-ischemic encephalopathy LLT
    Population Age: Newborns, Under 18 Gender: Male, Female
    Trial protocol: FR (Completed)
    Trial results: (No results available)
    EudraCT Number: 2020-000140-58 Sponsor Protocol Number: NL7255100000 Start Date*: 2020-07-23
    Sponsor Name:Leiden University Medical Center
    Full Title: Complement Inhibition: Attacking the Overshooting Inflammation @fter Traumatic Brain Injury - A phase II trial on the safety and efficacy of C1 esterase inhibitor Cinryze for the acute management o...
    Medical condition: Severe traumatic Brain Injury (TBI) with GCS < 13
    Disease: Version SOC Term Classification Code Term Level
    20.1 100000004863 10060690 Traumatic brain injury LLT
    Population Age: Adults Gender: Male, Female
    Trial protocol: NL (Trial now transitioned)
    Trial results: (No results available)
    EudraCT Number: 2007-000293-23 Sponsor Protocol Number: 2007-01 Start Date*: 2007-05-10
    Sponsor Name:Karolinska Universitetssjukhuset i Solna, Thoraxanestesi & intensivvård
    Full Title: Narkosgas jämfört med konventionell intravenös sedering vid respiratorvård efter kranskärlskirurgi.
    Medical condition: Studiegruppen består av kranskärlssjuka patienter som efter genomgången kranskärlskirurgi respiratorvårdas vid thoraxintensivvårdsavdelningen, enligt gängse postoperativ rutin, fram tills att förhå...
    Disease: Version SOC Term Classification Code Term Level
    9.1 10012208 Delayed recovery from anesthesia LLT
    9.1 10006894 CABG LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: SE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2010-022428-58 Sponsor Protocol Number: PRECONII Start Date*: 2010-09-21
    Sponsor Name:Aarhus University Hospital, Skejby
    Full Title: PRECON 2 – Fast-track cardiac surgery (kvalitetssikringsprojekt). Remifentanyl anæstesi til koronar bypass (CABG) med eller uden samtidig udskiftning af aortaklappen (AVR) bedømt ved opvågningsforl...
    Medical condition: Anæstesi til hjertekirurgiske patienter.Studiet er randomiseret med inklusion af patienter til elektiv CABG med/ uden samtidig AVR med anvendelse af cardiopulmonal bypass. Patienter randomiseres ti...
    Disease: Version SOC Term Classification Code Term Level
    12.1 10002092 Anaesthesia and allied procedures HLT
    12.1 10007530 Cardiac complications of anaesthesia or other sedation in labour and delivery LLT
    12.1 10012206 Delayed recovery from anaesthesia LLT
    12.1 10021722 Induction and maintenance anaesthesia LLT
    12.1 10031777 Other complications of anaesthesia or other sedation in labour and delivery LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: (No results available)
    EudraCT Number: 2011-003248-36 Sponsor Protocol Number: 61383082 Start Date*: 2011-09-30
    Sponsor Name:Central Military Hospital
    Full Title: The clinical significance of epigenetic factors research to refine the diagnosis, estimate prognosis and risk of recurrence after curative pancreatic cancer resection.
    Medical condition: The aim of the study to estimate frequence of epigenetics changes in pancreatic cancer and to assess the signidicance of apllication of the intravenous contrast agent during endosonography to bette...
    Disease: Version SOC Term Classification Code Term Level
    14.0 10018065 - General disorders and administration site conditions 10016335 Feeling hot and cold LLT
    14.0 10040785 - Skin and subcutaneous tissue disorders 10037872 Rash NOS LLT
    14.0 10037175 - Psychiatric disorders 10032168 Other insomnia LLT
    14.0 10007541 - Cardiac disorders 10008481 Chest pain - cardiac LLT
    14.0 10017947 - Gastrointestinal disorders 10064907 Functional abdominal pain LLT
    14.0 10029205 - Nervous system disorders 10048324 Dizziness aggravated LLT
    14.0 10029205 - Nervous system disorders 10033777 Paraesthesia distal LLT
    14.0 10022891 - Investigations 10050786 Fasting blood glucose increased LLT
    14.0 10018065 - General disorders and administration site conditions 10022096 Injection site reaction NOS LLT
    14.0 10021881 - Infections and infestations 10034838 Pharyngitis NOS LLT
    14.0 10018065 - General disorders and administration site conditions 10016259 Fatigueability LLT
    14.0 10021428 - Immune system disorders 10020762 Hypersensitivity type I LLT
    14.0 10028395 - Musculoskeletal and connective tissue disorders 10048412 Back pain aggravated LLT
    14.0 10021428 - Immune system disorders 10020756 Hypersensitivity reaction LLT
    14.0 10017947 - Gastrointestinal disorders 10028822 Nauseated LLT
    14.0 10047065 - Vascular disorders 10048347 Flushing aggravated LLT
    14.0 10029205 - Nervous system disorders 10024857 Loss of consiousness LLT
    14.0 10029205 - Nervous system disorders 10019218 Headache NOS LLT
    14.0 10040785 - Skin and subcutaneous tissue disorders 10037096 Pruritus NOS LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: CZ (Completed)
    Trial results: (No results available)
    EudraCT Number: 2007-001887-55 Sponsor Protocol Number: SCO/BIA-2093-305 Start Date*: 2007-10-12
    Sponsor Name:BIAL - Portela & Ca, S.A.
    Full Title: Efficacy and safety of eslicarbazepine acetate (BIA 2-093) as adjunctive therapy for refractory partial seizures in children: a double-blind, randomised, placebo-controlled, parallel-group, multice...
    Medical condition: children and adolescents with refractory partial epileptic seizures
    Disease: Version SOC Term Classification Code Term Level
    14.1 10029205 - Nervous system disorders 10015037 Epilepsy PT
    Population Age: Children, Adolescents, Under 18, Adults Gender: Male, Female
    Trial protocol: PT (Completed) HU (Completed) CZ (Completed) AT (Completed) FR (Completed) SK (Completed) IT (Completed) ES (Completed) GB (Completed) DE (Completed)
    Trial results: View results
    Download Options:
    Number of Trials to download:
    Download Content:
    Download Format:
    Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial.
    « Previous 1  2 
    Query did not match any studies.
    For support, Contact us.
    The status and protocol content of GB trials is no longer updated since 1 January 2021. For the UK, as of 31 January 2021, EU Law applies only to the territory of Northern Ireland (NI) to the extent foreseen in the Protocol on Ireland/NI. Legal notice
    As of 31 January 2023, all EU/EEA initial clinical trial applications must be submitted through CTIS . Updated EudraCT trials information and information on PIP/Art 46 trials conducted exclusively in third countries continues to be submitted through EudraCT and published on this website.

    European Medicines Agency © 1995-Fri May 23 18:54:52 CEST 2025 | Domenico Scarlattilaan 6, 1083 HS Amsterdam, The Netherlands
    EMA HMA