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Clinical trials for Pain management

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   44341   clinical trials with a EudraCT protocol, of which   7370   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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    489 result(s) found for: Pain management. Displaying page 1 of 25.
    1  2  3  4  5  6  7  8  9  Next» Last»»
    EudraCT Number: 2008-000239-17 Sponsor Protocol Number: 08-PP-03 Start Date*: 2008-05-06
    Sponsor Name:CHU de NICE
    Full Title: Use of MEOPA by elderly with dementia
    Medical condition: PAIN DUE TO BEDSORE OR WOUND BY ELDERLY WITH DEMENTIA
    Disease: Version SOC Term Classification Code Term Level
    9.1 10056350 Pain management LLT
    Population Age: Elderly Gender: Male, Female
    Trial protocol: FR (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2010-020547-13 Sponsor Protocol Number: 201001 Start Date*: 2011-08-24
    Sponsor Name:Foot and Ankle Surgical center
    Full Title: A randomized study comparing etoricoxib and diclofenac sodium in post hallux valgus surgery pain
    Medical condition: Postoperative pain
    Disease: Version SOC Term Classification Code Term Level
    12.1 10056350 Pain management PT
    Population Age: Adults Gender: Male, Female
    Trial protocol: SE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2009-011233-27 Sponsor Protocol Number: 09/WNo02/7 Start Date*: 2009-09-10
    Sponsor Name:North Wales NHS Trust
    Full Title: Comparison of efficacy of concentration with volume of local anaesthetics in femoral-sciatic blocks for total knee replacement
    Medical condition: No medical condition or disease under investigation.
    Disease: Version SOC Term Classification Code Term Level
    9.1 10002182 Analgesia LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: GB (Prematurely Ended)
    Trial results: (No results available)
    EudraCT Number: 2009-011458-16 Sponsor Protocol Number: N/A Start Date*: 2009-09-10
    Sponsor Name:North Wales NHS Trust
    Full Title: Comparison of efficacy and side effects of intrathecal fentanyl with intrathecal morphine
    Medical condition: Analgesia
    Disease: Version SOC Term Classification Code Term Level
    9.1 10002182 Analgesia LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: GB (Prematurely Ended)
    Trial results: (No results available)
    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: 2011-002935-24 Sponsor Protocol Number: 1.0 Start Date*: 2011-09-08
    Sponsor Name:The Princess Alexandra Hospital NHS Trust
    Full Title: A pilot study comparing the effectiveness of peripheral nerve block in forefoot surgery for post-operative pain relief when administered at the beginning rather than at the end of surgery.
    Medical condition: Post-operative pain control following forefoot sugery
    Disease: Version SOC Term Classification Code Term Level
    14.0 10042613 - Surgical and medical procedures 10056350 Pain management PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: GB (GB - no longer in EU/EEA)
    Trial results: (No results available)
    EudraCT Number: 2011-001783-21 Sponsor Protocol Number: 3288 Start Date*: 2012-07-11
    Sponsor Name:Childrens's Research Institute
    Full Title: Optimizing Pain Treatment in Pre-Term Neonates
    Medical condition: Critically Ill Premature Neonates between 23 and 32 weeks of gestation who are receiving morphine as part of their routine medical management of pain or other medically indicated condition for whic...
    Disease: Version SOC Term Classification Code Term Level
    14.1 10042613 - Surgical and medical procedures 10056350 Pain management PT
    Population Age: Preterm newborn infants, Under 18 Gender: Male, Female
    Trial protocol: NL (Prematurely Ended)
    Trial results: (No results available)
    EudraCT Number: 2019-000178-50 Sponsor Protocol Number: 2gas Start Date*: 2019-06-19
    Sponsor Name:Medical University of Graz
    Full Title: Perioperative off-label application (from admission up to 72 hours postoperatively) of Fentanyl TTS as part of a pain management in comparison to a certified pain medication management in adult pat...
    Medical condition: Elderly Patientens with hip-fracture (ICD-10 72.01-72.2)
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: AT (Completed)
    Trial results: (No results available)
    EudraCT Number: 2013-000384-87 Sponsor Protocol Number: AGO/2013/001 Start Date*: 2013-03-05
    Sponsor Name:Ghent University Hospital
    Full Title: Intraperitoneal atomization of levobupivacaine during gynecological laparoscopic procedures : Impact on pain, opioid use and length of recovery room stay (IPLA).
    Medical condition: Patients who are planned for gynecological laparoscopic interventions on an ambulatory basis.
    Disease: Version SOC Term Classification Code Term Level
    14.1 100000004865 10002182 Analgesia LLT
    Population Age: Adults Gender: Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2004-001201-10 Sponsor Protocol Number: FEN-PPA-401 Start Date*: 2004-07-26
    Sponsor Name:JANSSEN-CILAG
    Full Title: Comparison of transdermal fentanyl PCA and IV morphine PCA in the management of post-operative pain control.
    Medical condition: Treatment of moderate to severe post-operative pain in subjects who have undergone an elective major abdominal or orthopaedic surgical procedure.
    Disease: Version SOC Term Classification Code Term Level
    6.1 10056350 PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Completed) ES (Completed)
    Trial results: View results
    EudraCT Number: 2007-003976-20 Sponsor Protocol Number: GRC6211-201 Start Date*: 2007-09-12
    Sponsor Name:GLENMARK PHARMACEUTICALS SA
    Full Title: A randomised, double blind, placebo and active controlled, parallel group study to evaluate the analgesic effect of a single dose of GRC 6211, a TRPV1 receptor antagonist on pain following third...
    Medical condition: treatment of pain following third molar extraction
    Disease: Version SOC Term Classification Code Term Level
    10056350 PT
    Population Age: Adults Gender: Male, Female
    Trial protocol: IT (Prematurely Ended)
    Trial results: (No results available)
    EudraCT Number: 2006-006820-21 Sponsor Protocol Number: P060501 Start Date*: 2007-03-28
    Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP)
    Full Title: Réduction de la douleur lors des prélèvements veineux chez le nouveau-né prématuré : apport de la crème Emla et du saccharose
    Medical condition: Nouveau-nés prématurés hospitalisés dans les services de néonatologie de l'hôpital d'enfants Armand-Trousseau et du Centre Hospitalier de Meaux
    Disease: Version SOC Term Classification Code Term Level
    8.1 10056350 Pain management PT
    Population Age: Preterm newborn infants, Under 18 Gender: Male, Female
    Trial protocol: FR (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2018-000314-38 Sponsor Protocol Number: PSS2018/DEXPED-MEISTELMAN/YB Start Date*: 2018-09-11
    Sponsor Name:CHRU de NANCY
    Full Title: Efficiency of IV dexamethasone compared to placebo, administrated after a lower limb blockade is done, on the post operative pain in children : a controled, randomised, double blind study.
    Medical condition: post operative pain
    Disease: Version SOC Term Classification Code Term Level
    20.0 100000004865 10002182 Analgesia LLT
    Population Age: Children, Adolescents, Under 18 Gender: Male, Female
    Trial protocol: FR (Prematurely Ended)
    Trial results: (No results available)
    EudraCT Number: 2009-014983-20 Sponsor Protocol Number: DIA001 Start Date*: 2010-02-25
    Sponsor Name:Wockhardt UK Limited
    Full Title: An open label single dose pharmacokinetic study of Diamorphine Hydrochloride Nasal Spray (0.06mg/kg) in children
    Medical condition: The IMP is to be used as an analgesic for the relief of acute pain.
    Disease: Version SOC Term Classification Code Term Level
    12.0 10002182 Analgesia LLT
    Population Age: Infants and toddlers, Children, Adolescents, Under 18 Gender: Male, Female
    Trial protocol: GB (Prematurely Ended)
    Trial results: (No results available)
    EudraCT Number: 2009-014982-16 Sponsor Protocol Number: DIA002 Start Date*: 2010-02-25
    Sponsor Name:Wockhardt UK Limited
    Full Title: An open label, single dose safety study of Diamorphine Hydrochloride Nasal Spray (0.1mg/kg) in children
    Medical condition: The IMP is to be used as an analgesic for the relief of acute pain.
    Disease: Version SOC Term Classification Code Term Level
    12.0 10002182 Analgesia LLT
    Population Age: Children, Adolescents, Under 18 Gender: Male, Female
    Trial protocol: GB (Prematurely Ended)
    Trial results: (No results available)
    EudraCT Number: 2006-004001-26 Sponsor Protocol Number: 06AE001 Start Date*: 2007-02-23
    Sponsor Name:Nottingham University Hospitals NHS Trust
    Full Title: A Randomised Controlled Trial of Fascia Iliaca Compartment Block vs. Morphine For Pain in Fractured Neck of Femur in the Emergency Department: A Pilot Study
    Medical condition: Suspected isolated hip fracture - Clinical suspicion of hip fracture is defined as the presence of painful, unilateral shortening and external rotation of the lower limb preventing weight-bearing.
    Disease: Version SOC Term Classification Code Term Level
    8.1 10002182 Analgesia LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: GB (Completed)
    Trial results: View results
    EudraCT Number: 2015-003760-36 Sponsor Protocol Number: HUS277/03/2015 Start Date*: 2016-01-20
    Sponsor Name:HUS - Naistentautien ja synnytysten tulosyksikkö
    Full Title: Pain an medical abortion -Predicting factors of pain and optimal pain management among teenaged women compared to adult women
    Medical condition: Pain during Medical termination of pregnancy
    Disease:
    Population Age: Adolescents, Under 18, Adults Gender: Female
    Trial protocol: FI (Completed)
    Trial results: (No results available)
    EudraCT Number: 2013-000235-27 Sponsor Protocol Number: S-20120216 Start Date*: 2013-02-19
    Sponsor Name:Odense universitets Hospital
    Full Title: Interscalener blockade for surgery on the shoulder, a comparison of two dosing regimens: Fixed intermittent bolus with the possibility of PCA (Patient controlled administration) Vs. continuous infu...
    Medical condition: Shoulder frcture Rotator cuff leasion Shoulder alluplastic
    Disease: Version SOC Term Classification Code Term Level
    16.1 100000004865 10002182 Analgesia LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: View results
    EudraCT Number: 2008-008439-28 Sponsor Protocol Number: 1682/08 Start Date*: 2009-03-22
    Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI
    Full Title: Effects of the addition of haloperidol on propofol requirements during sedation with propofol and remifentanil
    Medical condition: analgo-sedation in mechanically ventilated patients
    Disease: Version SOC Term Classification Code Term Level
    9.1 10002182 Analgesia LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Completed)
    Trial results: (No results available)
    EudraCT Number: 2021-000304-38 Sponsor Protocol Number: ANTUKA Start Date*: 2021-04-06
    Sponsor Name:CHU de Poitiers
    Full Title: Tumescent anesthesia efficiency in pain management during a dynamic phototherapy session in vertex actinic keratosis treatment: a single-center prospective randomized study.
    Medical condition:
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: FR (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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