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Clinical trials for General anesthesia

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
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    • 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   44339   clinical trials with a EudraCT protocol, of which   7369   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 ).  
     
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    368 result(s) found for: General anesthesia. Displaying page 5 of 19.
    « Previous 1  2  3  4  5  6  7  8  9  Next» Last»»
    EudraCT Number: 2018-002258-56 Sponsor Protocol Number: SD-DXP Start Date*: 2018-08-27
    Sponsor Name:University Hospitals Leuven
    Full Title: The use of xenon and dexmedetomidine for the prevention of postoperative emergence delirium after anaesthesia for pediatric cardiac catheterization: A randomized, controlled, observer-blinded pilot...
    Medical condition: xenon-dexmedetomidine Anesthesia in children undergoing cardiac catheterization
    Disease:
    Population Age: Newborns, Infants and toddlers, Children, Under 18 Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2012-002834-36 Sponsor Protocol Number: Retro-001 Start Date*: 2012-09-13
    Sponsor Name:UMCG
    Full Title: Evaluation of the effects of the addition of atropine during propofol/remifentanil induction of anesthesia on hemodynamics, microvascular blood flow and tissue oxygenenation in patients undergoing ...
    Medical condition: ophthalmic surgery
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: NL (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2017-001011-36 Sponsor Protocol Number: ICO-A-2016-04 Start Date*: 2017-05-24
    Sponsor Name:INSTITUT DE CANCEROLOGIE DE L'OUEST
    Full Title: Multicentric, comparative, randomized, open study comparing an early post-operative prophylactic non-invasive ventilation (NIV) to standard post-operative care in patients at high-risk of respir...
    Medical condition: Legally adult patient going to have an operation under loco-regional or general anesthesia.
    Disease: Version SOC Term Classification Code Term Level
    19.1 10022117 - Injury, poisoning and procedural complications 10072651 Postoperative respiratory failure PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: FR (Completed)
    Trial results: View results
    EudraCT Number: 2018-000656-18 Sponsor Protocol Number: 2042015 Start Date*: 2018-11-09
    Sponsor Name:SINTETICA SA
    Full Title: Randomized, multi-center, double-blind, two-armed, parallel active groups, prospective trial, to evaluate, in pediatric population undergoing 'Calcaneo stop' surgery or Inguinal hernia repair, the ...
    Medical condition: Pediatric patients undergoing surgery of flatfoot or inguinal hernia
    Disease: Version SOC Term Classification Code Term Level
    20.0 100000004865 10002325 Anesthesia local LLT
    Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 Gender: Male, Female
    Trial protocol: IT (Trial now transitioned) ES (Restarted)
    Trial results: (No results available)
    EudraCT Number: 2010-021022-35 Sponsor Protocol Number: 0908125 Start Date*: 2010-10-12
    Sponsor Name:CHU de Saint-Etienne
    Full Title: Effet of curarization under general anaesthesia on eye movements in non-strabismus children
    Medical condition: Healthy volunteer who will have a surgery requiring curare administration (amygdalectomy...)
    Disease: Version SOC Term Classification Code Term Level
    12.1 10042609 Surgery LLT
    12.1 10057290 Curarization LLT
    Population Age: Children, Adolescents, Under 18 Gender: Male, Female
    Trial protocol: FR (Completed)
    Trial results: (No results available)
    EudraCT Number: 2007-005279-32 Sponsor Protocol Number: NeuroMorfeo - FARM6FKJKK Start Date*: 2007-12-10
    Sponsor Name:A.O. San Gerardo di Monza
    Full Title: ANESTHESIOLOGICAL STRATEGIES IN ELECTIVE CRANIOTOMY: RANDOMIZED, EQUIVALENCE, OPEN TRIAL
    Medical condition: Study population. This is a multicenter randomized, open label, controlled trial, utilizing an equivalence design and evaluating three different anesthesiological strategies in patients undergoin...
    Disease: Version SOC Term Classification Code Term Level
    9.1 10053302 Nervous system surgery LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Completed)
    Trial results: View results
    EudraCT Number: 2008-007996-26 Sponsor Protocol Number: RC 47/07 Start Date*: 2008-12-15
    Sponsor Name:ISTITUTO PER L`INFANZIA BURLO GAROFOLO
    Full Title: Comparison between wound infiltration with different ropivacaine concentrations following inguinal herniotomy for postoperative analgesia in children: a randomized, double-blind, placebo-controlle...
    Medical condition: Children ASA 1-2, aged 1 to 8 years.
    Disease: Version SOC Term Classification Code Term Level
    9.1 10021945 Infiltration anaesthesia LLT
    Population Age: Infants and toddlers, Children, Under 18 Gender: Male, Female
    Trial protocol: IT (Prematurely Ended)
    Trial results: (No results available)
    EudraCT Number: 2007-007951-14 Sponsor Protocol Number: 19.4.318 Start Date*: 2008-05-05
    Sponsor Name:NV Organon
    Full Title: A multi-center, randomized, parallel-group, comparative, active-controlled, safety-assessor blinded trial in adult subjects comparing the efficacy and safety of sugammadex administered at 1-2 PTC w...
    Medical condition: Not applicable
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: FI (Completed) GB (Completed) DE (Completed)
    Trial results: View results
    EudraCT Number: 2015-000051-24 Sponsor Protocol Number: RemiPedEntropy_v1.0 Start Date*: 2015-03-26
    Sponsor Name:Klaus Olkkola/University of Helsinki
    Full Title: The pharmacokinetics and –genomics of remifentanil, and its effects on the depth-of-anaesthesia monitors and the protein synthesis in children.
    Medical condition: otherwise healthy patients undergoing an operation necessitating general anaesthesia
    Disease:
    Population Age: Children, Adolescents, Under 18 Gender: Male, Female
    Trial protocol: FI (Completed)
    Trial results: (No results available)
    EudraCT Number: 2019-002200-40 Sponsor Protocol Number: MEV90-TQL-ZUH Start Date*: 2019-07-04
    Sponsor Name:Anæstesiologisk afdeling, Sjællands Universitetshospital, Roskilde
    Full Title: The minimal effective volume (MEV90) of ropivacaine 0.75 % for ultrasound-guided transmuscular quadratus lumborum block for unilateral percutaneous nephrolitotomy – A dose finding study.
    Medical condition: Postoperative pain following percutaneous nephrolithotomy.
    Disease: Version SOC Term Classification Code Term Level
    20.0 100000004865 10059805 Nephrolithotomy LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: (No results available)
    EudraCT Number: 2010-024185-22 Sponsor Protocol Number: Start Date*: 2011-06-08
    Sponsor Name:Med. Univ. Wien, Klinik für Anästhesie, Allgemeine Intensivmedizin und Schmerztherapie
    Full Title: Prospective, Randomized Clinical Pilot Study: Use of Lidocaine/Tetracaine Patch (Rapydan®) for Topical Anesthesia before Aterial Access
    Medical condition: Rapydan, ein neuartiges Schmerzpflaster, enthält zwei Lokalanästhetika (Lidocain und Tetracain) in höherer Dosierung (jeweils 70mg) als herkömmliche topische Schmerzpflaster. Die Studie soll zeigen...
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: AT (Completed)
    Trial results: View results
    EudraCT Number: 2014-002147-18 Sponsor Protocol Number: ABR49503 Start Date*: 2015-07-02
    Sponsor Name:Academic Medical Center
    Full Title: A randomized controlled double-blinded trial comparing the effect of on Demand ROcuronium boluses vs continuous infusion on rating of surgical and anesthesia conditions and need for reversal in Pat...
    Medical condition: oesophageal carcinoma
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: NL (Completed)
    Trial results: (No results available)
    EudraCT Number: 2006-002890-31 Sponsor Protocol Number: Pregab1 Start Date*: 2006-08-25
    Sponsor Name:Dept. of Anaesthesia, Medical University of Vienna
    Full Title: Does Pregabalin reduce preoperative anxiety: a placebo controlled study
    Medical condition: Patients should receive Pregabalin or placebo as premedication one hour before ambulatory elective surgery. After this they have to assess their anxiety and pain with Visual Analog Scale (VAS) for ...
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: AT (Completed)
    Trial results: View results
    EudraCT Number: 2013-000905-22 Sponsor Protocol Number: 5505 Start Date*: 2013-07-09
    Sponsor Name:Hôpitaux Universitaires de Strasbourg
    Full Title: à compléter
    Medical condition: akathisia
    Disease: Version SOC Term Classification Code Term Level
    18.0 10029205 - Nervous system disorders 10001540 Akathisia PT
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: FR (Completed)
    Trial results: (No results available)
    EudraCT Number: 2018-004512-22 Sponsor Protocol Number: P2018/568 Start Date*: 2019-02-18
    Sponsor Name:Erasme University Hospital
    Full Title: Effect of dexmedetomidine vs 0.9% sodium chloride on Nol-Index guided remifentanil analgesia: a double-blinded bicenter randomized controlled trial
    Medical condition: Intraoperative analgesia during general anesthesia
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2019-004121-25 Sponsor Protocol Number: NMBA_ELDERLY2019ROCU_REMI Start Date*: 2019-12-17
    Sponsor Name:Rigshospitalet
    Full Title: A single-blinded multicenter randomized study comparing intubating conditions after either rocuronium 0.6 mg/kg or remifentanil 2 µg/kg in elderly patients.
    Medical condition: The aim of this study is to determine the effect on intubating conditions and laryngeal morbidity after either rocuronium 0.6 mg/kg or remifentanil 2 µg/kg in patients with age ≥ 80 years.
    Disease: Version SOC Term Classification Code Term Level
    21.1 100000004865 10002323 Anesthesia general LLT
    Population Age: Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: View results
    EudraCT Number: 2011-004733-14 Sponsor Protocol Number: GSKET102011 Start Date*: 2012-03-22
    Sponsor Name:Medizinische Universität Wien
    Full Title: Intravenous S-Ketamine as an Analgesic Adjunct to General Anesthesia in chronic opioid-tolerant patient
    Medical condition: In the present investigation, we will compare the perioperative subanesthetic infusion of ketamine with placebo in opioid-resistant patients undergoing major orthopedic surgery. By powering the stu...
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: AT (Prematurely Ended)
    Trial results: View results
    EudraCT Number: 2016-002323-28 Sponsor Protocol Number: prop01 Start Date*: 2016-06-28
    Sponsor Name:Universitair Ziekenhuis Brussel
    Full Title: Blood concentration and pharmacokinetic analysis of propofol following administration of single induction dose in small children
    Medical condition: Children scheduled for elective surgery
    Disease:
    Population Age: Infants and toddlers, Children, Under 18 Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2013-002247-28 Sponsor Protocol Number: SM2-RS-2013 Start Date*: 2013-07-04
    Sponsor Name:Rigshospitalet
    Full Title: The effect of chlorzoxazone of moderate to severe postoperative pain after back surgery
    Medical condition: Patients set to back surgery in general anesthesia
    Disease: Version SOC Term Classification Code Term Level
    16.0 100000004865 10036236 Postoperative pain relief LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: (No results available)
    EudraCT Number: 2011-000157-23 Sponsor Protocol Number: version1.1SFINX Start Date*: 2011-09-27
    Sponsor Name:UMC St Radboud
    Full Title: Street Fitness In surgical patieNts undergoing general anesthesia after reversal of neuromuscular rest blockade with sugammadeX (SFINX study)
    Medical condition: Males and females in the age of 18-65 undergoing minor surgery/gynaecological procedures with a medical need for general anesthesia and neuromuscular blockade will be included in the study.
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: NL (Completed)
    Trial results: View results
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    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.

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