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Clinical trials for Intercostal nerve

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   44335   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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    6 result(s) found for: Intercostal nerve. Displaying page 1 of 1.
    EudraCT Number: 2006-006444-63 Sponsor Protocol Number: Version 1.0 Start Date*: 2007-06-14
    Sponsor Name:VO Anesthesia/ICU Lunds University Hospital
    Full Title: The addition of clonidine to bupivacaine/adrenaline intercostal nerve blockades in patients undergoing open cholecystectomies
    Medical condition: duration and quality of postoperative pain control with intercostal nerve blockade after open cholecystectomies
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: SE (Prematurely Ended)
    Trial results: (No results available)
    EudraCT Number: 2012-003275-19 Sponsor Protocol Number: 402-C-322 Start Date*: 2013-01-29
    Sponsor Name:Pacira Pharmaceuticals, Inc.
    Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study to Assess the Efficacy and Safety of Intercostal Nerve Block with Liposome Bupivacaine in Subjects Undergo...
    Medical condition: Intercostal Nerve Block for Posterolateral Thoracotomy
    Disease: Version SOC Term Classification Code Term Level
    14.1 100000004865 10038286 Regional nerve block LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: CZ (Completed) PL (Completed) BG (Completed)
    Trial results: View results
    EudraCT Number: 2021-006201-29 Sponsor Protocol Number: SC102021 Start Date*: 2022-04-28
    Sponsor Name:University Hospitals Leuven
    Full Title: Erector spinae plane (ESP) block versus intercostal nerve blocks (ICNB) in uniportal videoscopic assisted thoracic surgery (VATS): A multicenter double-blind, prospective, randomized controlled trial.
    Medical condition: Postoperative pain treatment after uniportal videoscopic assisted thoracic surgery (VATS).
    Disease: Version SOC Term Classification Code Term Level
    21.1 100000004865 10036236 Postoperative pain relief LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2021-003218-38 Sponsor Protocol Number: AAUH-VATS-01 Start Date*: 2021-09-08
    Sponsor Name:Aalborg University Hospital
    Full Title: Pain after thoracoscopic lung surgery – the effect of intercostal nerve blockades with standard bupivacaine and liposomal bupivacaine – a randomised controlled feasibility trial
    Medical condition: Acute postoperative pain Lung cancer
    Disease: Version SOC Term Classification Code Term Level
    20.0 100000004864 10025044 Lung cancer LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Prematurely Ended)
    Trial results: View results
    EudraCT Number: 2013-001829-76 Sponsor Protocol Number: ProsMaMa13.1 Start Date*: 2013-10-04
    Sponsor Name:Paula Diéguez García
    Full Title: INTERCOSTAL BRANCHES BLOCK IN THE MIDAXILLARY LINE VERSUS PARAVERTEBRAL BLOCK, ULTRASOUND-GUIDED FOR NOT RECONSTRUCTIVE BREAST SURGERY. RANDOMIZED CLINICAL TRIAL
    Medical condition: Sheduled patients for nor reconstructive unilateral breast surgery
    Disease: Version SOC Term Classification Code Term Level
    16.0 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps) 10057654 Breast cancer female PT
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2020-004584-11 Sponsor Protocol Number: 10140021910007 Start Date*: 2021-02-03
    Sponsor Name:Maxima MC
    Full Title: Optimal postoperative Pain management After Lung surgery (OPtriAL): multi-centre randomised trial
    Medical condition: Acute postoperative pain after lung surgery
    Disease: Version SOC Term Classification Code Term Level
    20.1 100000004863 10054711 Postoperative pain LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: NL (Ongoing)
    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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