Flag of the European Union EU Clinical Trials Register Help

Clinical trials for Epidural analgesia

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   44347   clinical trials with a EudraCT protocol, of which   7375   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
     
    135 result(s) found for: Epidural analgesia. Displaying page 5 of 7.
    « Previous 1  2  3  4  5  6  7  Next»
    EudraCT Number: 2008-001236-13 Sponsor Protocol Number: 2008-001236-13 Start Date*: 2007-12-01
    Sponsor Name:AZIENDA OSPEDALIERA DI PADOVA
    Full Title: Sperimental controlled and randomized in singol blind study. Use of continuous epidural ketamina in patients submitted to toracotomy for pulmonary resection.
    Medical condition: pulmonary resection
    Disease: Version SOC Term Classification Code Term Level
    9.1 10038738 SOC
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2009-014832-38 Sponsor Protocol Number: 2009.558 Start Date*: 2010-01-18
    Sponsor Name:Hospices Civils de Lyon
    Full Title: Analgésie par Bloc Paravertébral après Vidéothoracoscopie. Etude comparative : Ropivacaïne versus Ropivacaïne et Sufentanil
    Medical condition: analgésie post-opératoire
    Disease: Version SOC Term Classification Code Term Level
    12.0 10036276 Postoperative analgesia LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: FR (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2010-018600-87 Sponsor Protocol Number: Peri-Trauma Start Date*: 2010-02-24
    Sponsor Name:AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA` DI NOVARA
    Full Title: POST-OPERATIVE PAIN CONTROL OF PEDIATRIC PATIENTS UNDERWENT ORTHOPEDIC SURGERY: COMPARISON OF INTRAVENOUS ANALGESIA AND ONE-SHOT EPIDURAL LUMBAR NERVE BLOCK.
    Medical condition: POST-OPERATIVE PAIN CONTROL OF PEDIATRIC PATIENTS UNDERWENT ORTHOPEDIC SURGERY
    Disease: Version SOC Term Classification Code Term Level
    9.1 10028395 SOC
    Population Age: Children, Adolescents, Under 18 Gender: Male, Female
    Trial protocol: IT (Completed)
    Trial results: (No results available)
    EudraCT Number: 2010-018548-15 Sponsor Protocol Number: GALLSPA001 Start Date*: 2012-03-23
    Sponsor Name:Anestesicentrum, Sundsvalls Sjukhus, Landstinget Västernorrland
    Full Title: Spinal vs intercostal block for analgesia after open cholecystectomy - differences in postoperative pain?
    Medical condition: Analgesia after open cholecystectomy.
    Disease: Version SOC Term Classification Code Term Level
    14.1 10042613 - Surgical and medical procedures 10008611 Cholecystectomy PT
    Population Age: Gender: Male, Female
    Trial protocol: SE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2014-002044-41 Sponsor Protocol Number: 38RC14.176 Start Date*: 2014-08-18
    Sponsor Name:University Hospital of Grenoble
    Full Title:
    Medical condition:
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: FR (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2006-002456-15 Sponsor Protocol Number: ANE 05/06 Start Date*: 2006-06-29
    Sponsor Name:UZ Leuven
    Full Title: The influence of prophylactic ephedrine on arterial hypotension and fetal dysrhythmia after combined spinal-epidural anesthesia during labour
    Medical condition: Comined spinal - epiural analgesia (CSE) during labour.
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: BE (Prematurely Ended)
    Trial results: View results
    EudraCT Number: 2013-000556-17 Sponsor Protocol Number: CIR-TAP-2012 Start Date*: 2013-03-25
    Sponsor Name:Fundació Parc Taulí
    Full Title: Randomized clinical trial to compare the control of postoperative pain in laparoscopic sigmoidectomy by administering local anesthetic epidural catheter analgesia with intravenous morphine patient-...
    Medical condition: Postoperative pain
    Disease: Version SOC Term Classification Code Term Level
    14.1 100000004863 10054711 Postoperative pain LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2016-000813-63 Sponsor Protocol Number: TACs Start Date*: 2016-04-06
    Sponsor Name:Universitair Ziekenhuis Brussel
    Full Title: Comparative doubleblind study with prilocaine 2 % and 2-chloroprocaine for elective caesarean section.
    Medical condition: Healthy pregnant women undergoing a elective caesarean section with an uncomplicated pregnancy of a singleton, "full-term", all between 18-40 y (ASAI-II) through combined spinal and epidural approach.
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2009-015659-26 Sponsor Protocol Number: 2009-015659-26 Start Date*: 2010-01-22
    Sponsor Name:Karolinska Institutet
    Full Title: Cortical and hormonal stress responses to pain management with morphine in standard clinical dosage
    Medical condition: Neonatal pain
    Disease: Version SOC Term Classification Code Term Level
    12.1 10056350 Pain management LLT
    12.1 10022519 Intensive care LLT
    12.1 10029392 Newborn LLT
    Population Age: Preterm newborn infants, Newborns, Under 18 Gender: Male, Female
    Trial protocol: SE (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2014-001857-17 Sponsor Protocol Number: ANE-BUP-2014-01 Start Date*: 2014-10-20
    Sponsor Name:Carlos Fernandez Galvan
    Full Title: Evaluating the effectiveness of TAP and management epidural morphine chloride in Caesarean sections.
    Medical condition: Caesarean delivery
    Disease: Version SOC Term Classification Code Term Level
    17.0 100000004865 10006921 Caesarean delivery (infant record) LLT
    Population Age: Adults Gender: Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2008-000529-20 Sponsor Protocol Number: FENHYDPAI4012 Start Date*: 2008-05-20
    Sponsor Name:Janssen-Cilag Limited
    Full Title: Comparison of Ionsys® and routine care with morphine IV PCA in the management of early post-operative mobilisation, ability to mobilise and in time to Fitness For Discharge (FFD)
    Medical condition: Evaluation of the mobilisation characteristics, clinical use, safety and Ease of Care (EOC) of a Fentanyl Iontophoretic Transdermal PCA system (Ionsys) and morphine IV PCA for management of acute...
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: GB (Prematurely Ended)
    Trial results: View results
    EudraCT Number: 2008-007987-40 Sponsor Protocol Number: KetaminaEsse Start Date*: 2008-12-29
    Sponsor Name:AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA` DI NOVARA
    Full Title: Low dose intravenous ketamine (S) associated to thoracic epidural analgesia: effects on the “post-thoracotomy pain syndrome” (PTPS)
    Medical condition: All patients that will undergo to an elective thoracotomic surgery in the Hospital “Maggiore della Carita`” of Novara for a 12 months period.
    Disease: Version SOC Term Classification Code Term Level
    9.1 10042613 SOC
    9.1 10052703 LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Completed)
    Trial results: (No results available)
    EudraCT Number: 2008-008527-14 Sponsor Protocol Number: Q8012-001 Start Date*: 2009-06-02
    Sponsor Name:University of Witten/Herdecke
    Full Title: A Randomized, Double-Blind, Active Controlled Study Comparing the Intravenous Dose of Morphine and Oxycodone Combined in a Ratio of 1:1 Versus Morphine Alone Required to Achieve Effective Pain Cont...
    Medical condition: To determine whether the intravenous coadministration of morphine and oxycodone has fewer opioid related adverse effects (AEs) than morphine alone at doses that result in effective and equi-analges...
    Disease: Version SOC Term Classification Code Term Level
    9.1 10036276 Postoperative analgesia LLT
    9.1 10054710 Postoperative hip pain LLT
    Population Age: Elderly Gender: Male, Female
    Trial protocol: DE (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2015-002958-12 Sponsor Protocol Number: 2015-003-M Start Date*: 2015-09-15
    Sponsor Name:Reinier de Graaf Groep
    Full Title: Median Local Anaesthetic dose (MLAD) of Intrathecal Bupivacaine in total hip arthroplasty with the anterior approach.
    Medical condition: Spinal anesthesia during total hip arthroplasty with anterior approach
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: NL (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2016-000082-23 Sponsor Protocol Number: 2016-001-M Start Date*: 2016-03-11
    Sponsor Name:Reinier de Graaf Groep
    Full Title: Median Local Anaesthetic Dose (MLAD) of intrathecal Bupivacaine in total knee arthroplasty
    Medical condition: Spinal anaesthesia during total knee arthroplasty
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: NL (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2013-002449-12 Sponsor Protocol Number: 2013-002449-12 Start Date*: 2013-11-19
    Sponsor Name:Westfriesgasthuis
    Full Title: Does buprenorphine (Temgesic) 0,3 mg prolongs the analgesic effect of a blockade of the femoral nerve with 20 ml ropivacaïne HCL Fresenius Kabi 0,2% for patiënts with a total knee replacement. A pr...
    Medical condition: -
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: NL (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2015-001944-13 Sponsor Protocol Number: ZAA15CPP Start Date*: 2016-07-27
    Sponsor Name:Zaans Medisch Centrum
    Full Title: Chloroprocaine vs prilocaine for spinal anaesthesia in day-case surgery: a double-blind randomized trial
    Medical condition: Patients scheduled for ambulatory knee arthroscopy surgery receive one of the two spinal anaesthetics
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: NL (Completed)
    Trial results: View results
    EudraCT Number: 2007-003926-11 Sponsor Protocol Number: MVDV 07/2007 Start Date*: 2007-10-03
    Sponsor Name:University Hospitals Leuven
    Full Title: Low dose of ephedrine versus phenylephrine in the prevention of arterial hypotension after low dosed CSE for elective C-section : is there a difference in umbilical blood gas values ?
    Medical condition: combined spinal-epidural analgesia during C-section
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2009-017326-39 Sponsor Protocol Number: MVDV11/09 Start Date*: 2010-02-24
    Sponsor Name:University Hospitals Leuven
    Full Title: Vergelijkende studie tussen PCEA en TAP-block als postoperatieve pijnstilling bij setio-patiënten
    Medical condition: pain treatment after C-section
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: BE (Prematurely Ended)
    Trial results: View results
    EudraCT Number: 2018-001305-82 Sponsor Protocol Number: IC3627/18 Start Date*: 2019-05-16
    Sponsor Name:Laura Perelló Moreno
    Full Title: Study on the advantages of local post-operative infiltration in forefoot surgery.
    Medical condition: management of postoperative pain in ambulatory foot surgery that allows the realization of immediate rehabilitation and better functional results and personal satisfaction
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    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  3  4  5  6  7  Next»
    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-Sat Jul 05 13:06:11 CEST 2025 | Domenico Scarlattilaan 6, 1083 HS Amsterdam, The Netherlands
    EMA HMA