Flag of the European Union EU Clinical Trials Register Help

Clinical trials for Nerve block

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 ).  
     
    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
     
    166 result(s) found for: Nerve block. Displaying page 1 of 9.
    1  2  3  4  5  6  7  8  9  Next»
    EudraCT Number: 2016-004541-82 Sponsor Protocol Number: SupClun_1-1 Start Date*: 2016-12-19
    Sponsor Name:Dep. Anaesthesia and Intensive Care, Aarhus University Hospital
    Full Title: Regional anaesthesia of the cutaneous nerves of the hip - A novel ultrasound guided nerve block of the superior cluneal nerves
    Medical condition: Postoperative pain after hip surgery
    Disease: Version SOC Term Classification Code Term Level
    19.0 10022891 - Investigations 10022891 Investigations SOC
    Population Age: Adults Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: View results
    EudraCT Number: 2016-004377-41 Sponsor Protocol Number: TFP_1-1 Start Date*: 2016-12-19
    Sponsor Name:Dep. Anaesthesia and Intensive Care, Aarhus University Hospital
    Full Title: Regional anaesthesia of the cutaneus nerves of the hip - A randomized controlled trial of the transversalis fascia plane block
    Medical condition: Postoperative pain after hip surgery
    Disease: Version SOC Term Classification Code Term Level
    19.0 10022891 - Investigations 10022891 Investigations SOC
    Population Age: Adults Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: (No results available)
    EudraCT Number: 2008-008177-57 Sponsor Protocol Number: AN08/8748 Start Date*: 2009-06-05
    Sponsor Name:University of Leeds
    Full Title: “What is the ED95 dose of Prilocaine for femoral nerve block using ultrasound?”
    Medical condition:
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: GB (Completed)
    Trial results: View results
    EudraCT Number: 2022-000093-25 Sponsor Protocol Number: 01_20012022 Start Date*: 2022-05-05
    Sponsor Name:Aarhus University Hospital
    Full Title: The effect of lateral pectoral nerve block in combination with interscalene nerve block on opioid consumption and pain on awake shoulder arthroscopy patients - A feasibility study
    Medical condition: Peri- and postoperative pain after shoulder arthroscopy
    Disease: Version SOC Term Classification Code Term Level
    20.0 100000004848 10077421 Shoulder arthroscopy LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Prematurely Ended)
    Trial results: (No results available)
    EudraCT Number: 2013-004013-41 Sponsor Protocol Number: AUH-TFB-SSPS-3 Start Date*: 2015-09-18
    Sponsor Name:Thomas Fichnter Bendtsen
    Full Title: Supra Sacral Parallel Shift - ultrasound/MR image fusion guided lumbosacral plexus block
    Medical condition:
    Disease: Version SOC Term Classification Code Term Level
    18.0 100000004863 10054710 Postoperative hip pain LLT
    18.0 10042613 - Surgical and medical procedures 10051060 Hip surgery PT
    Population Age: Adults Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: View results
    EudraCT Number: 2009-013462-25 Sponsor Protocol Number: MW001 Start Date*: 2009-09-28
    Sponsor Name:NHS Greater Glasgow and Clyde Health Board
    Full Title: A dose finding study for ultrasound guided anterior psoas compartment blocks in patients with a fractured neck of femur
    Medical condition: Proximal traumatic fractured neck of femur
    Disease: Version SOC Term Classification Code Term Level
    10029173 Nerve block LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: GB (Completed)
    Trial results: View results
    EudraCT Number: 2013-005346-10 Sponsor Protocol Number: AUH-TFB-SR Start Date*: 2014-11-21
    Sponsor Name:Thomas Fichtner Bendtsen
    Full Title: Shamrock versus Lumbar Ultrasound Trident – Ultrasound guided block of the lumbar plexus
    Medical condition:
    Disease: Version SOC Term Classification Code Term Level
    17.1 100000004863 10054710 Postoperative hip pain LLT
    17.1 10042613 - Surgical and medical procedures 10051060 Hip surgery PT
    Population Age: Adults Gender: Male
    Trial protocol: DK (Completed)
    Trial results: View results
    EudraCT Number: 2015-002304-89 Sponsor Protocol Number: protocol2_2tdn Start Date*: 2015-07-30
    Sponsor Name:Thomas Fichtner Bendtsen
    Full Title: Preoperative analgesic affect of combined obturator and femoral nerve block compared to femoral nerve block alone, in patients with hip fracture.
    Medical condition: Hip fracture
    Disease: Version SOC Term Classification Code Term Level
    18.1 100000004863 10017284 Fractured femoral neck LLT
    Population Age: Adults Gender: Male, Female
    Trial protocol: DK (Prematurely Ended)
    Trial results: View results
    EudraCT Number: 2014-001702-18 Sponsor Protocol Number: protocol1tdn Start Date*: 2014-08-28
    Sponsor Name:Thomas Fichtner Bendtsen
    Full Title: Analgesic duration of a preoperative single-shot femoral nerve block with Bupivacaine and adjuvant Dexamethasone in patients with hip fracture
    Medical condition: Pain in patients with hip fracture
    Disease: Version SOC Term Classification Code Term Level
    17.1 100000004863 10017284 Fractured femoral neck LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Prematurely Ended)
    Trial results: View results
    EudraCT Number: 2022-003201-30 Sponsor Protocol Number: 1.0-03.10.2022 Start Date*: 2022-12-22
    Sponsor Name:Medical University Vienna
    Full Title: The Impact of Biological Gender in Peripheral Nerve Blockade: A Prospective Study in Volunteers
    Medical condition: To evaluate pharmacodynamic, pharmacokinetic and nerve-related morphometric differences of biological gender (male versus female) on nerve block characteristics
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: AT (Prematurely Ended)
    Trial results: View results
    EudraCT Number: 2010-023262-46 Sponsor Protocol Number: 20101005PH Start Date*: 2011-03-08
    Sponsor Name:Royal Devon & exeter Foundation trust
    Full Title: A Randomised Prospective Pilot Study Comparing the Outcomes of Patients with Lumbar Nerve Root Pain Secondary to Lumbar Disc Prolapse Treated by Nerve Root Block with or without the Addition of Clo...
    Medical condition: Lumbar nerve root pain secondary to disc prolapse.
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: GB (Completed)
    Trial results: View results
    EudraCT Number: 2017-002280-18 Sponsor Protocol Number: FIPRA#3 Start Date*: 2017-09-18
    Sponsor Name:Nordsjællands Hospital Hillerød
    Full Title: Catheter-based peripheral regional anaesthesia after orthopaedic surgery: Comparison of low dose, automated periodic infusions with conventional high dose, continuous infusion, and patient-initiat...
    Medical condition: Postoperative pain, after orthopaedic surgery.
    Disease: Version SOC Term Classification Code Term Level
    20.0 10042613 - Surgical and medical procedures 10029173 Nerve block PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: View results
    EudraCT Number: 2015-005544-33 Sponsor Protocol Number: AUH-TFB-SR-ULMR Start Date*: 2016-02-08
    Sponsor Name:Thomas Fichtner Bendtsen
    Full Title: Shamrock – Ultrasound/MR image fusion guided lumbar plexus blocks
    Medical condition: Hip surgery anaesthesia and perioperative analgesia
    Disease: Version SOC Term Classification Code Term Level
    18.1 100000004863 10036284 Post-operative hip pain LLT
    18.1 10042613 - Surgical and medical procedures 10051060 Hip surgery PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: View results
    EudraCT Number: 2014-000299-25 Sponsor Protocol Number: 1.4 Start Date*: 2014-12-05
    Sponsor Name:Unfallkrankenhaus Salzburg
    Full Title: Dexmedetomidine for saphenous nerve blockade in patients undergoing anterior cruciate ligament replacement: a randomized, placebo-controlled, triple blinded study
    Medical condition: Dexmedetomidine -a selective alpha-2-receptor agonist- added to a local anaesthetic (ropivacaine) should prolong a saphenous block and the patients demand for the first analgesic. We designed a pro...
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: AT (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2011-004285-15 Sponsor Protocol Number: SM2-PJ-11 Start Date*: 2011-09-22
    Sponsor Name:Professor Jørgen Berg Dahl
    Full Title: A comparison of the efficacy of the Adductor-Canal-Blockade vs. the femoral nerve block on muscle strength and mobilization in healthy volunteers: a randomized study
    Medical condition: Healthy volunteers (intended for postoperative pain treatment in patients after total knee arthroplasty)
    Disease: Version SOC Term Classification Code Term Level
    14.0 10022117 - Injury, poisoning and procedural complications 10054711 Postoperative pain LLT
    Population Age: Adults Gender: Male
    Trial protocol: DK (Completed)
    Trial results: View results
    EudraCT Number: 2016-004883-20 Sponsor Protocol Number: SM1-JH-16 Start Date*: 2017-02-01
    Sponsor Name:Ole Mathiesen
    Full Title: Does perineural dexmedetomidine prolong the duration of an ulnar nerve block when controlling for possible systemic effects? - a randomized, blinded, placebo controlled, paired trial in healthy vo...
    Medical condition: Healthy volunteers (treatment intended to improve regional anesthesia for orthopedic surgery)
    Disease: Version SOC Term Classification Code Term Level
    19.1 100000004863 10054711 Postoperative pain LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: View results
    EudraCT Number: 2015-000078-36 Sponsor Protocol Number: protocol2tdn Start Date*: 2015-03-17
    Sponsor Name:Thomas Fichtner Bendtsen
    Full Title: Analgetisk effekt af proksimal supplerende nervus obturatorius blokade efter insufficient analgetisk effekt af nervus femoralis blokade hos patienter med hoftenær femurfraktur
    Medical condition: Pain in patients with hip fracture
    Disease: Version SOC Term Classification Code Term Level
    17.1 100000004863 10017284 Fractured femoral neck LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Prematurely Ended)
    Trial results: View results
    EudraCT Number: 2023-000035-74 Sponsor Protocol Number: 1.1_27.02.2023 Start Date*: 2023-03-05
    Sponsor Name:Medical University Vienna
    Full Title: Pharmacodynamics of Liposomal Bupivacaine for Peripheral Nerve Blockade: A Randomized, Triple-blinded, Cross Over Study in Volunteers
    Medical condition: To evaluate the pharmacodynamic effects of perineural administered liposomal bupivacaine on nerve block characteristics
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: AT (Completed)
    Trial results: View results
    EudraCT Number: 2009-013481-10 Sponsor Protocol Number: 437 Start Date*: 2009-10-14
    Sponsor Name:Sint Maartenskliniek
    Full Title: Pharmacokinetics of high dose Ropivacaine with and without epinephrine for combined femoral and sciatic nerve block in lower extremity surgery. A pilot study.
    Medical condition: combined femoral and sciatic nerve block for lower extremity orthopedic surgery
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: NL (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2020-004942-12 Sponsor Protocol Number: Protokol_MFCN_10102020 Start Date*: 2020-11-19
    Sponsor Name:Aarhus University Hospital
    Full Title: Selective ultrasound-guided nerve block of the medial femoral cutaneous nerve in healthy volunteers
    Medical condition: Pain around the surgical incisions after total knee arthroplasty (TKA). The area anesthetized by new nerve block techniques anesthetizing the medial femoral cutaneous nerve are investigated in heal...
    Disease: Version SOC Term Classification Code Term Level
    21.1 100000004865 10036236 Postoperative pain relief LLT
    21.0 100000004865 10002325 Anesthesia local LLT
    20.1 10022891 - Investigations 10045434 Ultrasound scan PT
    Population Age: Adults Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: View results
    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.
    1  2  3  4  5  6  7  8  9  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-Fri May 09 22:26:10 CEST 2025 | Domenico Scarlattilaan 6, 1083 HS Amsterdam, The Netherlands
    EMA HMA