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Clinical trials for Spinal anesthesia

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
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    The EU Clinical Trials Register currently displays   44366   clinical trials with a EudraCT protocol, of which   7389   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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    120 result(s) found for: Spinal anesthesia. Displaying page 1 of 6.
    1  2  3  4  5  6  Next»
    EudraCT Number: 2007-000702-71 Sponsor Protocol Number: PreSpiDi2006-01 Start Date*: 2007-07-13
    Sponsor Name:Alysis Zorggroep
    Full Title: The effect of intravenous fluid preload on diuresis during spinal anesthesia-induced detrusor blockade
    Medical condition: Diuresis during spinal anesthesia
    Disease: Version SOC Term Classification Code Term Level
    9.1 10041538 Spinal anesthesia LLT
    9.1 10013523 Diuresis LLT
    Population Age: Adults Gender: Male, Female
    Trial protocol: NL (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2015-000882-29 Sponsor Protocol Number: 001 Start Date*: 2016-02-18
    Sponsor Name:Reinier de Graaf Groep
    Full Title: Spinal hyperbaric Prilocaine 2% 60 or 80 mg: a dosing study in day care patients.
    Medical condition: spinal anesthesia for open inguinal hernia repair or lower limb surgery
    Disease: Version SOC Term Classification Code Term Level
    18.1 100000004865 10041538 Spinal anesthesia LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: NL (Completed)
    Trial results: (No results available)
    EudraCT Number: 2004-004822-29 Sponsor Protocol Number: CHL1/02-2004 Start Date*: 2005-03-09
    Sponsor Name:SINTETICA SA
    Full Title: Spinal anaesthesia with 2 -chlopoprocaine 1% for lower limb procedures of short duration: a prospective randomized, blind, dose-finding study.
    Medical condition: Spinal anaesthesia for short therm surgical procedures
    Disease: Version SOC Term Classification Code Term Level
    6.1 10041536 PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Completed)
    Trial results: (No results available)
    EudraCT Number: 2018-003182-34 Sponsor Protocol Number: 2018-10 Start Date*: 2018-10-18
    Sponsor Name:CHR d'ORLEANS
    Full Title: Randomized, double-blind, controlled clinical trial for comparison of continuous phenylephrine versus norepinephrine infusion for maintenance of hemodynamic stability during cesarean section under...
    Medical condition: hypotension during caesarean section under spinal anesthesia
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: FR (Completed)
    Trial results: (No results available)
    EudraCT Number: 2019-003972-37 Sponsor Protocol Number: CLVSPR19 Start Date*: 2020-06-05
    Sponsor Name:Hospital Arnau de Vilanova - Lliria
    Full Title: Comparative study of cloroprocaine versus prilocaine intrathecal anestesia in major ambulatory surgery
    Medical condition: Inguinal hernia liable to ambulatory surgery
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2022-003178-22 Sponsor Protocol Number: 91255 Start Date*: 2022-11-16
    Sponsor Name:Unknown at this point Between jobs [...]
    1. Unknown at this point Between jobs
    2. Unknown at this point Between jobs
    Full Title: Intrathecal morphine versus sufentanil in ultra-low dose of isobaric bupivacaine in the management of postoperative pain in patients with hip fractures
    Medical condition: Patients Habile
    Disease: Version SOC Term Classification Code Term Level
    20.0 100000004865 10041537 Spinal anaesthesia (all forms) LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Prematurely Ended)
    Trial results: (No results available)
    EudraCT Number: 2014-003778-17 Sponsor Protocol Number: CHL.1/02-2014 Start Date*: 2015-02-23
    Sponsor Name:Sintetica S.A.
    Full Title: Spinal anaesthesia with Chloroprocaine HCl 1% for elective lower limb procedures of short duration: a prospective, randomised, observer-blind study in adult patients
    Medical condition: Short duration (less than 40 min) lower limb surgery via spinal anaesthesia
    Disease: Version SOC Term Classification Code Term Level
    17.1 10042613 - Surgical and medical procedures 10041536 Spinal anaesthesia PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Completed)
    Trial results: View results
    EudraCT Number: 2022-000857-10 Sponsor Protocol Number: NA Start Date*: 2022-05-16
    Sponsor Name:CHU de Liège
    Full Title: Isobaric versus hyperbaric intrathecal bupivacaine: influence of baricity on blood pression variation during elective total knee arthroplasty: a randomized clinical trial.
    Medical condition: Total knee arthroplasty
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2015-003498-13 Sponsor Protocol Number: HIP/FUSION#1 Start Date*: 2016-03-18
    Sponsor Name:Institut for Klinisk Medicin, Aarhus Universitet
    Full Title: Surgical anesthesia for elective hip surgery - hemodynamic effect of lumbosacral plexus blockade compared to continuous spinal anesthesia
    Medical condition: No specific medical condition is investigated. The objective of the investigation is to compare two methods for surgical anesthesia for total hip replacement.
    Disease: Version SOC Term Classification Code Term Level
    18.1 100000004865 10068084 Anesthesia procedure LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Prematurely Ended)
    Trial results: View results
    EudraCT Number: 2010-019669-27 Sponsor Protocol Number: 121 Start Date*: 2010-04-30
    Sponsor Name:University of Tartu
    Full Title: Hypobaric vs hyperbaric bupivacaine for spinal anaesthesia in total knee arthroplasty
    Medical condition: Orthopedic surgery patients with elective total knee arthroplasty
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: EE (Completed)
    Trial results: View results
    EudraCT Number: 2016-003010-26 Sponsor Protocol Number: B076201627677 Start Date*: 2018-01-11
    Sponsor Name:Centre Hospitalier Universitaire Saint Pierre , ULB
    Full Title: Hyperbaric Bupivacaine Versus Hyperbaric Prilocaine 2% for Cesarean Section Under Spinal Anesthesia: a Randomised and Controlled Clinical Trial
    Medical condition: Parturients undergoing an elective caesarean section performed under spinal anaesthesia
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: BE (Prematurely Ended)
    Trial results: (No results available)
    EudraCT Number: 2007-001176-37 Sponsor Protocol Number: 07/S1401/27 Start Date*: 2007-05-29
    Sponsor Name:NHS Tayside
    Full Title: A randomised, controlled trial to determine the median effective concentration of bupivacaine, levobupivacaine and ropivacaine after intrathecal and extradural injection for pain relief in the firs...
    Medical condition: Pain in early labour
    Disease: Version SOC Term Classification Code Term Level
    9.1 10054891 Epidural analgesia LLT
    9.1 10041536 Spinal anaesthesia LLT
    9.1 10059204 Labour pain LLT
    Population Age: Adults Gender: Female
    Trial protocol: GB (Prematurely Ended)
    Trial results: View results
    EudraCT Number: 2011-003675-11 Sponsor Protocol Number: AT06/2011 Start Date*: 2011-09-21
    Sponsor Name:University Hospitals Leuven
    Full Title: Comparison of 2-chloroprocaïne, bupivacaïne and lidocaïne for spinal anesthesia in knee artroscopy in an outpatient setting: a double blind randomised trial
    Medical condition: spinal anesthesia in knee arthroscopy
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2016-002397-12 Sponsor Protocol Number: 2016-011-M Start Date*: 2016-08-11
    Sponsor Name:Reinier de Graaf Groep
    Full Title: Median Local Anaesthetic dose (MLAD) of Intrathecal Prilocaïne 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: 2011-000062-35 Sponsor Protocol Number: ThereIsNoSponsorInvolved Start Date*: 2011-04-05
    Sponsor Name:Mikko Pitkänen, MD, PhD
    Full Title: Artikaiini 40mg ja kloroprokaiini 40 mg päiväkirurgisina spinaalipuudutteina (Lyhenne: A40C40)
    Medical condition: Knee arthroscopy performed as day case surgery
    Disease: Version SOC Term Classification Code Term Level
    12.1 10054948 Meniscus operation LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: FI (Completed)
    Trial results: View results
    EudraCT Number: 2017-000068-14 Sponsor Protocol Number: HIP/FUSION#2 Start Date*: 2017-05-24
    Sponsor Name:Institut for Klinisk Medicin, Aarhus Universitet
    Full Title: Postoperative analgesia after elective hip surgery - effect of obturator nerve blockade
    Medical condition: No specific medical condition is investigated. The objective of the trial is to investigate a method for postoperative analgesia after elective hip surgery.
    Disease: Version SOC Term Classification Code Term Level
    19.1 100000004865 10068084 Anesthesia procedure LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: View results
    EudraCT Number: 2007-000968-25 Sponsor Protocol Number: CHL1/02-2006/M; INN60M2006 Start Date*: 2007-07-16
    Sponsor Name:SINTETICA ITALIA S.R.L.
    Full Title: Prospective, blind observer, randomised clinical study to investigate and compare the efficacy of intrathecal plain solutions containing Chloroprocaine 1% (50 mg) versus Bupivacaine 0.5% (10 mg)
    Medical condition: patients undergoing elective short-duration (< 40 min) in low abdominal (gynaecology and urology disciplines) or lower limbs (no more than 1/3 of cases) surgery under spinal anaesthesia.
    Disease: Version SOC Term Classification Code Term Level
    9.1 10041536 Spinal anaesthesia LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Completed) DE (Completed)
    Trial results: View results
    EudraCT Number: 2014-001947-18 Sponsor Protocol Number: ISIS396443-CS4 Start Date*: 2015-07-07
    Sponsor Name:Ionis Pharmaceuticals, Inc.
    Full Title: A Phase 3, Randomized, Double-blind, Sham-Procedure Controlled Study to Assess the Clinical Efficacy and Safety of ISIS 396443 Administered Intrathecally in Patients with Later-onset Spinal Muscula...
    Medical condition: Spinal Muscular Atrophy (SMA)
    Disease: Version SOC Term Classification Code Term Level
    19.0 10010331 - Congenital, familial and genetic disorders 10041582 Spinal muscular atrophy PT
    Population Age: Children, Adolescents, Under 18 Gender: Male, Female
    Trial protocol: DE (Completed) GB (Completed) SE (Completed) ES (Completed) IT (Completed) FR (Ongoing)
    Trial results: View results
    EudraCT Number: 2015-002843-32 Sponsor Protocol Number: 54015 Start Date*: 2016-09-20
    Sponsor Name:
    Full Title: The haemodynamic effects of spinal anaesthesia with versus without sufentanil added to bupivacaine heavy
    Medical condition: Patient undergoing surgery for which they receive spinal anaesthesia
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: NL (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)
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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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