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Clinical trials for Sufentanil

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   44334   clinical trials with a EudraCT protocol, of which   7366   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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    84 result(s) found for: Sufentanil. Displaying page 1 of 5.
    1  2  3  4  5  Next»
    EudraCT Number: 2009-013801-33 Sponsor Protocol Number: 201010 Start Date*: 2009-10-07
    Sponsor Name:Steen W. Henneberg, Børnesmerteenheden, Anæstesi afd. 4013, Juliane Marie Centeret, Rigshospitalet
    Full Title: Nasal administration af sufentanil+ketamin til procedure-relaterede smerter hos børn.
    Medical condition: Procedure-relaterede smerter hos børn
    Disease: Version SOC Term Classification Code Term Level
    12.0 10049124 Sedation during medical procedure LLT
    Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: (No results available)
    EudraCT Number: 2012-002533-10 Sponsor Protocol Number: SuRe-001 Start Date*: 2013-05-22
    Sponsor Name:UMCG
    Full Title: Comparison of the effects of atropine on haemodynamics and tissue oxygenation in anaesthesia with propofol and sufentanil versus propofol and remifentanil’
    Medical condition: Comparison of the effects of atropine on haemodynamics and tissue oxygenation in anaesthesia with propofol and sufentanil versus propofol and remifentanil
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: NL (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2011-003648-31 Sponsor Protocol Number: PKPDHM-001 Start Date*: 2011-11-17
    Sponsor Name:Universitätsklinikum Erlangen
    Full Title: Pharmacokinetic-pharmacodynamic modeling of the postoperative pain sensation during patient-controlled analgesia with target-controlled infusion of Hydromorphone, taking into account the interactio...
    Medical condition: Pain therapy after elective cardiac surgery
    Disease: Version SOC Term Classification Code Term Level
    14.0 10042613 - Surgical and medical procedures 10036236 Postoperative pain relief LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DE (Completed)
    Trial results: View results
    EudraCT Number: 2009-014741-89 Sponsor Protocol Number: 0916202 Start Date*: 2009-10-20
    Sponsor Name:Centre Hospitalier de Toulouse
    Full Title: Recherche de la DE90 d'un bolus de sufentanil pour l'analgésie des soins douloureux de nursing des malades intubés de réanimation
    Medical condition: patients intubés en réanimation sous ventilation mécanique
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: FR (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2006-005614-12 Sponsor Protocol Number: 10.0 Start Date*: 2007-05-18
    Sponsor Name:Medical University Vienna
    Full Title: CSE at Vaginal Delivery - MLAD of Ropivacain and the Effect of Sufentanil
    Medical condition: Dose-finding study of Ropivacain 5% with different doses of Sufentanil intrathecal at the combined spinal epidural anesthesia at labouring patients. If patients are requesting analgesia during labo...
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: AT (Completed)
    Trial results: View results
    EudraCT Number: 2015-001721-16 Sponsor Protocol Number: 2014_09 Start Date*: 2015-07-24
    Sponsor Name:Centre Hospitalier Régional et Universitaire de Lille
    Full Title: SUFENTANIL maternal and foetal pharmacokinetic evaluation after intra–amniotic injection
    Medical condition:
    Disease: Version SOC Term Classification Code Term Level
    18.0 10022891 - Investigations 10053098 Foetal and neonatal investigations HLGT
    Population Age: In utero, Under 18, Adults Gender: Female
    Trial protocol: FR (Completed)
    Trial results: (No results available)
    EudraCT Number: 2015-002843-32 Sponsor Protocol Number: 54015 Start Date*: 2016-09-20
    Sponsor Name:
    Full Title: The haemodynamic effects of spinal anaesthesia with versus without sufentanil added to bupivacaine heavy
    Medical condition: Patient undergoing surgery for which they receive spinal anaesthesia
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: NL (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2018-000016-19 Sponsor Protocol Number: PSCs Start Date*: 2018-04-04
    Sponsor Name:Universitair ziekenhuis Brussel
    Full Title: Randomized comparative double blind prospective study with hyperbaric prilocaine 2 % and 3 different doses of sufentanil for elective caesarean section.
    Medical condition: Healthy pregnant women
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: BE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2017-004038-28 Sponsor Protocol Number: Zalviso Start Date*: 2018-02-21
    Sponsor Name:Universitair Ziekenhuis Brussel
    Full Title: Comparative Prospective Randomized Study in Postoperative Cardiac Surgery Patients on Analgesia with Morphine Continuous Infusion or Sublingual Sufentanil (Zalviso®).
    Medical condition: -Postoperative pain treatment after cardiac surgery
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2008-003621-16 Sponsor Protocol Number: ALLAI1 Start Date*: 2008-08-19
    Sponsor Name:ERASME HOSPITAL
    Full Title: Utilisation du sufentanil en péridural lors du travail obstétrical: étude des répercussions sur le nouveau-né et l'allaitement maternel
    Medical condition: BREAST FEEDING
    Disease: Version SOC Term Classification Code Term Level
    9.1 10006248 Breast feeding problem (infant) LLT
    Population Age: Adults Gender: Female
    Trial protocol: BE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2016-001603-23 Sponsor Protocol Number: RBHP_2016_FUTIER Start Date*: 2017-03-08
    Sponsor Name:CHU de Clermont-Ferrand
    Full Title: .
    Medical condition: .
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: FR (Completed)
    Trial results: (No results available)
    EudraCT Number: 2008-005712-40 Sponsor Protocol Number: 1253/08 Start Date*: 2008-09-19
    Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI
    Full Title: Evaluation of postoperative pain management with thoracic paravertebral block using levobupivacaine associated with sufentanil
    Medical condition: postoperative pain
    Disease: Version SOC Term Classification Code Term Level
    9.1 10036286 Post-operative pain LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Completed)
    Trial results: (No results available)
    EudraCT Number: 2021-003258-21 Sponsor Protocol Number: PDC-01-0205 Start Date*: 2022-05-19
    Sponsor Name:Cessatech A/S
    Full Title: Analgesic Efficacy and Pharmacokinetic-pharmacodynamic Relationship of Intranasally Administered Sufentanil, Ketamine, and CT001 after Impacted Mandibular Third Molar Extraction
    Medical condition: Healthy male or female participants scheduled for surgical removal of an impacted mandibular third molar, where bone removal is judged to be needed.
    Disease: Version SOC Term Classification Code Term Level
    21.0 100000004865 10050327 Dental surgery NOS LLT
    Population Age: Adults Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: View results
    EudraCT Number: 2022-003178-22 Sponsor Protocol Number: 91255 Start Date*: 2022-11-16
    Sponsor Name:Unknown at this point Between jobs [...]
    1. Unknown at this point Between jobs
    2. Unknown at this point Between jobs
    Full Title: Intrathecal morphine versus sufentanil in ultra-low dose of isobaric bupivacaine in the management of postoperative pain in patients with hip fractures
    Medical condition: Patients Habile
    Disease: Version SOC Term Classification Code Term Level
    20.0 100000004865 10041537 Spinal anaesthesia (all forms) LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Prematurely Ended)
    Trial results: (No results available)
    EudraCT Number: 2007-005544-24 Sponsor Protocol Number: Sufentanil/Fentanyl in toracotomia Start Date*: 2007-06-20
    Sponsor Name:AZIENDA OSPEDALIERA DI PADOVA
    Full Title: Sperimental, controlled, randomized single blind study. Sufentanil vs fentanyl in patientes with thoracotomy for pulmonary resection and videolaparoscopic surgery.
    Medical condition: Patientes with thoracotomy for pulmonary resection and videolaparoscopic surgery.
    Disease: Version SOC Term Classification Code Term Level
    9.1 10062043 Lung operation LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Completed)
    Trial results: (No results available)
    EudraCT Number: 2020-004488-14 Sponsor Protocol Number: PDC01-0204 Start Date*: 2021-02-10
    Sponsor Name:Cessatech A/S
    Full Title: Bioavailability study of intranasal sufentanil/ketamine fixed combination in healthy volunteers
    Medical condition: Not applicable - healthy volunteers
    Disease: Version SOC Term Classification Code Term Level
    22.0 10022891 - Investigations 10022891 Investigations SOC
    Population Age: Adults Gender: Male
    Trial protocol: DK (Completed)
    Trial results: View results
    EudraCT Number: 2009-017665-31 Sponsor Protocol Number: CSE Start Date*: 2010-09-30
    Sponsor Name:AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA` DI NOVARA
    Full Title: Effect on mother and fetus of epidural and combined spinal-epidural techniques for labour analgesia
    Medical condition: Labour
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: IT (Completed)
    Trial results: (No results available)
    EudraCT Number: 2009-015752-22 Sponsor Protocol Number: gymoese007 Start Date*: 2009-11-24
    Sponsor Name:Bent Gymoese Jørgensen
    Full Title: Tilsætning af sufentanil til interskalenerblokade ved skulderoperation
    Medical condition: Postoperative smerter efter arthroskopisk skulderoperation
    Disease: Version SOC Term Classification Code Term Level
    12.0 10003393 Arthropathy, unspecified, involving shoulder region LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: (No results available)
    EudraCT Number: 2019-001232-59 Sponsor Protocol Number: AGO/2019/002 Start Date*: 2020-01-29
    Sponsor Name:Ghent University Hospital
    Full Title: Safety and Efficacy of Patient Controlled Analgesia using the Sublingual Sufentanil Tablet System (SSTS) in a fast track rehabilitation program after Total Knee Arthroplasty.
    Medical condition: Total Knee Arthroplasty
    Disease: Version SOC Term Classification Code Term Level
    21.1 10042613 - Surgical and medical procedures 10036276 Postoperative analgesia PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2013-001665-16 Sponsor Protocol Number: 1312 Start Date*: 2013-08-01
    Sponsor Name:University Hospital Grenoble
    Full Title: Intranasal Sufentanyl analgesia Versus Morphine IV in Emergency room.
    Medical condition:
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: FR (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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