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Clinical trials for Alfentanil

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   43881   clinical trials with a EudraCT protocol, of which   7295   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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    17 result(s) found for: Alfentanil. Displaying page 1 of 1.
    EudraCT Number: 2018-000026-54 Sponsor Protocol Number: 18662008 Start Date*: 2018-09-12
    Sponsor Name:Medicinkliniken, Sjukhuset Lidköping
    Full Title: A comparison of sedatives used during gastroscopy, alfentanil vs midazolam
    Medical condition: Sedative effect during gastroscopy
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: SE (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2014-005170-11 Sponsor Protocol Number: UCLDexAlf1 Start Date*: 2015-01-26
    Sponsor Name:Cliniques universitaires Saint Luc
    Full Title: Can we get conscious sedation in optimal safety conditions in an emergency department, by combining dexmedetomidine with alfentanil?
    Medical condition: Adult over 18 years, of both sexes, for which a procedural sedation is needed in emergency room.
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2021-003821-31 Sponsor Protocol Number: Futurum-963747 Start Date*: 2022-03-15
    Sponsor Name:Region Jönköping, Sweden [...]
    1. Region Jönköping, Sweden
    2. Region Östergötland, Sweden
    Full Title: Patient-controlled Sedation in Port Implantation (PACSPI 2)- a randomized controlled trial
    Medical condition: Patients ≥18 years with cancer in need of subcutaneous venous port will be offered to participate in the trial. The aim of the trial is to determine if patient-controlled sedation (PCS) with prop...
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: SE (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2011-001903-10 Sponsor Protocol Number: OX51-002 Start Date*: 2012-08-07
    Sponsor Name:Orexo AB
    Full Title: A randomized, double-blind, placebo-controlled, dose finding trial using sublingual alfentanil to alleviate pain associated with a prostate biopsy procedure
    Medical condition: Pain associated with prostate biopsy.
    Disease: Version SOC Term Classification Code Term Level
    16.0 10022891 - Investigations 10004857 Biopsy prostate PT
    Population Age: Adults, Elderly Gender: Male
    Trial protocol: FI (Completed) CZ (Completed) ES (Completed) DK (Completed)
    Trial results: View results
    EudraCT Number: 2006-007053-51 Sponsor Protocol Number: 003/APR06 Start Date*: 2007-07-02
    Sponsor Name:Gloucestershire Hospitals NHS Foundation Trust
    Full Title: Diamorphine or alfentanil for subcutaneous use in hospice in-patients
    Medical condition: Palliative Care
    Disease: Version SOC Term Classification Code Term Level
    9.1 10059513 Palliative care LLT
    9.1 10059513 Palliative care PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: GB (Completed)
    Trial results: View results
    EudraCT Number: 2015-002667-42 Sponsor Protocol Number: ABR53999 Start Date*: 2015-09-09
    Sponsor Name:AMC
    Full Title: Sedation with propofol TCI during ERCP: Is the combination with esketamine more effective and safer than with alfentanil (SPEKA): A randomized controlled multicentre trial
    Medical condition: Patients undergoing ERCPs under propofol sedation combined with ketamine or alfentanil given by trained anesthesia nurse.
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: NL (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2011-004206-19 Sponsor Protocol Number: ABR36861 Start Date*: 2012-01-12
    Sponsor Name:AMC
    Full Title: Patient and Endoscopist Satisfaction with DEXmedetomidine versus Propofol/Alfentanil sedation during oesophagus interventions (PESDEX).
    Medical condition: Patients undergoing therapeutically esophageal interventions under sedation (dexmedetomidine or propofol/alfentanil) given by trained anesthesia nurse.
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: NL (Completed)
    Trial results: View results
    EudraCT Number: 2009-017274-20 Sponsor Protocol Number: 0927 Start Date*: Information not available in EudraCT
    Sponsor Name:Centre Hospitalier Universitaire de GRENOBLE
    Full Title: Evaluation de l’efficacité de l’Alfentanil chez l’enfant en réanimation infantile par rapport au Sufentanil - traitement de référence - sur le confort du patient lors de l’aspiration trachéale
    Medical condition: confort de l'enfant lors de l'aspiration trachéale en réanimation pédiatrique
    Disease:
    Population Age: Infants and toddlers, Children, Adolescents, Under 18 Gender: Male, Female
    Trial protocol: FR (Ongoing)
    Trial results: View results
    EudraCT Number: 2016-001373-33 Sponsor Protocol Number: 2016-3 Start Date*: 2017-02-17
    Sponsor Name:Region Ostergotland
    Full Title: Clinical Study Protocol An open phase IV,RCT, evaluating patient controlled sedation, in three different dosages of propofol in healthy subjects undergoing elective gynaecological out-patient su...
    Medical condition: Gynecological outpatient surgery
    Disease:
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: SE (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2006-004415-22 Sponsor Protocol Number: 632-31 Start Date*: 2007-02-19
    Sponsor Name:Karolinska University Hospital
    Full Title: Utvärdering av två oloika strategier att smärtbehandla patienter som genomgår ablationsbehandling mot hjärtrytmrubbningar i hjärtat
    Medical condition: Patients undergoing catheter ablation due to arrhythmias.
    Disease: Version SOC Term Classification Code Term Level
    8.1 10016566 Fibrillation atrial LLT
    Population Age: Gender: Male, Female
    Trial protocol: SE (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2012-001849-41 Sponsor Protocol Number: DOX-101 Start Date*: 2012-06-18
    Sponsor Name:Leids Universitair Medisch Centrum (LUMC)
    Full Title: Two-part, Randomized, Placebo-controlled, Repeated Stepped Infusion Dose Study of the Pharmacodynamics of Doxapram when Co-administered with Opioids (Protocol – doxapram-101).
    Medical condition: acute respiratory insufficiency, including such conditions as opioid and anesthetic-induced respiratory depression, post-anesthetic atelectasis, and central apneas (e.g., apnea of prematurity).
    Disease: Version SOC Term Classification Code Term Level
    14.1 10038738 - Respiratory, thoracic and mediastinal disorders 10038738 Respiratory, thoracic and mediastinal disorders SOC
    Population Age: Adults Gender: Male
    Trial protocol: NL (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2012-005528-13 Sponsor Protocol Number: 30112012 Start Date*: 2014-06-17
    Sponsor Name:Helsinki University Hospital
    Full Title: Comparison of Novel Articaine Lozenge Versus Placebo for Upper Gastrointestinal Endoscopy in Adults. A Randomized Double-blinded Controlled Study
    Medical condition: Patients who undergo esophagogastroduodenoscopy procedure for a first time
    Disease: Version SOC Term Classification Code Term Level
    17.0 10022891 - Investigations 10014819 Endoscopy upper gastrointestinal tract PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: FI (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2015-005489-46 Sponsor Protocol Number: OPEGG Start Date*: 2016-02-02
    Sponsor Name:Umeå University
    Full Title: Recovery of gastric function after treatment with shortacting opioids.
    Medical condition: The effect of opioids on gastric electrical activity
    Disease: Version SOC Term Classification Code Term Level
    18.1 100000004856 10018043 Gastroparesis LLT
    18.1 10022117 - Injury, poisoning and procedural complications 10018044 Gastroparesis postoperative PT
    18.1 100000004856 10021227 Idiopathic gastroparesis LLT
    Population Age: Adults Gender: Male, Female
    Trial protocol: SE (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2020-005177-27 Sponsor Protocol Number: 2020-005177-27 Start Date*: 2021-09-22
    Sponsor Name:Bispebjerg Hospital
    Full Title: Preoperative Viscous Lidocaine for Upper Gastrointestinal Endoscopy
    Medical condition: Topical local anesthesia for upper gastrointestinal endoscopy
    Disease: Version SOC Term Classification Code Term Level
    21.1 100000004865 10024760 Local anesthetic LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2009-012398-36 Sponsor Protocol Number: a003c Start Date*: 2009-06-18
    Sponsor Name:Helsinki University Hospital
    Full Title: Patient-controlled sedation with propofol in ERCP:alfentanyl vs remifentanyl
    Medical condition: Billiar tract and pancreatic disoderes
    Disease: Version SOC Term Classification Code Term Level
    9.1 10004676 Biliary tract disease LLT
    9.1 10004677 Biliary tract disorder NOS LLT
    9.1 10033616 Pancreatic disorder LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: FI (Completed)
    Trial results: (No results available)
    EudraCT Number: 2021-002816-30 Sponsor Protocol Number: 01072021 Start Date*: 2021-11-12
    Sponsor Name:Department of Anaesthesiology, Aarhus University Hospital
    Full Title: Individualised perioperative blood pressure and fluid therapy in oesophagectomy - Study protocol for a prospective randomised controlled trial
    Medical condition: Oesophagectomy
    Disease: Version SOC Term Classification Code Term Level
    20.0 10042613 - Surgical and medical procedures 10030215 Oesophagectomy PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2009-014862-25 Sponsor Protocol Number: a004c Start Date*: 2010-01-22
    Sponsor Name:Helsinki University Central Hospital
    Full Title: Dexmedetomidine vs placebo in ERCP sedation
    Medical condition: ERCP(Endoscopic retrograde cholangiopancreatography)
    Disease: Version SOC Term Classification Code Term Level
    12.1 10049192 Pancreatic fistula LLT
    12.1 10052108 Pancreatic duct stone LLT
    12.1 10033634 Pancreatic therapeutic procedures HLT
    12.1 10033615 Pancreatic cyst LLT
    12.1 10033616 Pancreatic disorder LLT
    12.1 10033635 Pancreatic pseudocyst LLT
    12.1 10052377 Pancreatic sphincterotomy LLT
    12.1 10015115 ERCP LLT
    Population Age: Adults Gender: Male, Female
    Trial protocol: FI (Completed)
    Trial results: (No results available)
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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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