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Clinical trials for Ropivacaine

The European Union Clinical Trials Register   allows you to search for protocol and results information on:
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    The EU Clinical Trials Register currently displays   43881   clinical trials with a EudraCT protocol, of which   7295   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).

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    217 result(s) found for: Ropivacaine. Displaying page 1 of 11.
    1  2  3  4  5  6  7  8  9  Next» Last»»
    EudraCT Number: 2012-002769-37 Sponsor Protocol Number: cervikalblock Start Date*: 2012-10-23
    Sponsor Name:UK für Anästhesiologie und allgemeine Intensivmedizin, LKH Salzburg
    Full Title: Influence of the concentration of the local anesthetic ropivacaine in the quality of a ultrasound guided block of the regio collis lateralis for carotid endarterectomy: a prospective, randomized an...
    Medical condition: Regional anesthesia for carotid endarterectomy surgery.
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: AT (Completed)
    Trial results: (No results available)
    EudraCT Number: 2014-004713-91 Sponsor Protocol Number: ROPISPINE Start Date*: 2015-02-09
    Sponsor Name:Universitair Ziekenhuis Brussel
    Full Title: Epidural ropivacaine as part of a multimodal postoperative pain treatment following thoracolumbar spinal fusion surgery.
    Medical condition: Spine Surgery
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: BE (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2019-004813-15 Sponsor Protocol Number: VERSPLASMA Start Date*: 2021-03-19
    Sponsor Name:AZ Turnhout
    Full Title: Serum concentrations of ropivacaine after unilateral pectoral nerve block type II (Pecs II) in breast cancer surgery
    Medical condition: The aim of this study is to quantify peak and mean venous serum concentrations of ropivacaine after ultrasound guided Pecs II block with 2.5mg/kg ropivacaine diluted to 30ml.
    Disease:
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: BE (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2021-000574-29 Sponsor Protocol Number: Esprobot001 Start Date*: 2021-09-22
    Sponsor Name:FUNDACIÓ CLÍNIC PER A LA RECERCA BIOMÈDICA
    Full Title: Erector Spinae Plane block in robotic cardiac surgery
    Medical condition: Postoperative pain
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2007-005835-27 Sponsor Protocol Number: S-VF-20060072 Start Date*: 2008-01-10
    Sponsor Name:Odense University Hospital
    Full Title: Local Infiltration with Ropivacaine for Postoperative Analgesia after Hip Fracture
    Medical condition: The effect of local infiltration with ropivacaine for postoperative analgesia after hip fracture is evaluated.
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: View results
    EudraCT Number: 2017-000180-32 Sponsor Protocol Number: 761 Start Date*: 2017-02-10
    Sponsor Name:Sint Maartenskliniek Nijmegen
    Full Title: Pharmacokinetic Profile of Ropivacaine after Periarticular Local Infiltration Analgesia for Primary Total Knee Arthroplasty Without the use of a Tourniquet.
    Medical condition: patients receiving primary total knee replacement
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: NL (Completed)
    Trial results: (No results available)
    EudraCT Number: 2009-013707-63 Sponsor Protocol Number: 1 Start Date*: 2010-03-05
    Sponsor Name:C.U.B ERASME HOSPITAL
    Full Title: POSTOPERATIVE ANALGESIA USING PREPERITONEAL CONTINUOUS INFUSIONS OF ROPIVACAINE IN PATIENTS UNDERGOING LIVER SURGERY -CONSEQUENCES ON ROPIVACAINE METABOLISM
    Medical condition: PATIENTS WITH HEPATIC TUMORS BUT WITH A GOOD HEPATIC FUNCTION BEFORE SURGERY
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: BE (Ongoing)
    Trial results: (No results available)
    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: 2019-002200-40 Sponsor Protocol Number: MEV90-TQL-ZUH Start Date*: 2019-07-04
    Sponsor Name:Anæstesiologisk afdeling, Sjællands Universitetshospital, Roskilde
    Full Title: The minimal effective volume (MEV90) of ropivacaine 0.75 % for ultrasound-guided transmuscular quadratus lumborum block for unilateral percutaneous nephrolitotomy – A dose finding study.
    Medical condition: Postoperative pain following percutaneous nephrolithotomy.
    Disease: Version SOC Term Classification Code Term Level
    20.0 100000004865 10059805 Nephrolithotomy LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: (No results available)
    EudraCT Number: 2014-005596-90 Sponsor Protocol Number: NL51548.100.14 Start Date*: 2015-04-22
    Sponsor Name:St. Lucas Andreas Hospital
    Full Title: Comparison of femoral nerve block with posterior capsule infiltration versus anterior and posterior capsule infiltration after total knee replacement.
    Medical condition: patienst requiring total knee replacement for non-inflammatory osteoarthritis of the knee
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: NL (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2009-015236-15 Sponsor Protocol Number: NILA/01/09 Start Date*: 2010-01-22
    Sponsor Name:Department of Surgery, National University of Ireland
    Full Title: NEBULISED INTRAPERITONEAL LOCAL ANAESTHETIC (NILA) FOR LAPAROSCOPIC SURGERY: A PROSPECTIVE, RANDOMISED, DOUBLE BLINDED, PLACEBO CONTROLLED CLINICAL TRIAL
    Medical condition: Post operative shoulder tip pain following laparoscopic appendectomy, cholecystectomy, laparoscopic Nissen fundoplication or diagnostic laparoscopy.
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IE (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2009-013397-40 Sponsor Protocol Number: vial1 Start Date*: 2009-11-05
    Sponsor Name:maternite régionale de nancy
    Full Title: Intérêt du bloc au triangle de Petit pour la prise en charge de l'analgésie de la chirurgie gynécologique lourde
    Medical condition: le but de ce travail est de déterminer l'efficacité analgésique du bloc au triangle de petit dans l'analgésie postopératoire des hystérectomies.
    Disease:
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: FR (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2008-002724-29 Sponsor Protocol Number: RC 48/07 Start Date*: 2011-10-26
    Sponsor Name:ISTITUTO PER L'INFANZIA BURLO GAROFOLO
    Full Title: Continuous peritoneal infusion of ropivacaine following laparoscopy for postoperative analgesia in children: a randomized, double-blind, placebo-controlled study.
    Medical condition: Children aged over 1 year, undergoing elective abdominal laparoscopic surgery.
    Disease: Version SOC Term Classification Code Term Level
    9.1 10023693 Laparoscopy LLT
    Population Age: Infants and toddlers, Children, Adolescents, Under 18 Gender: Male, Female
    Trial protocol: IT (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2011-002484-21 Sponsor Protocol Number: GernerDex00 Start Date*: 2011-07-22
    Sponsor Name:Universitätsklinik für Anästhesie - Paracelsus Medizinische Universität Salzburg
    Full Title: Comparison of ultrasound guided interscalene brachial plexus block with 10 ml vs 20 ml ropivacaine 0.5%
    Medical condition: different volumes (10 vs 20mL) of ropvacaine 0.5 %will be investigated, when used for interscalene brachial plexus block in shoulder surgery
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: AT (Prematurely Ended)
    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: 2010-019393-32 Sponsor Protocol Number: LEVOROPI Start Date*: 2005-08-05
    Sponsor Name:OSPEDALE POLICLINICO S. MATTEO
    Full Title: Evaluation of pharmacokinetics of levobupivacaine and ropivacaine during epidural infusion
    Medical condition: Major surgery
    Disease: Version SOC Term Classification Code Term Level
    9.1 10042613 SOC
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Completed)
    Trial results: (No results available)
    EudraCT Number: 2016-002786-62 Sponsor Protocol Number: CHD065-16 Start Date*: 2017-04-14
    Sponsor Name:Centre Hospitalier Départemental Vendée
    Full Title:
    Medical condition:
    Disease: Version SOC Term Classification Code Term Level
    20.0 10042613 - Surgical and medical procedures 10015087 Episiotomy PT
    Population Age: Adults Gender: Female
    Trial protocol: FR (Ongoing)
    Trial results: View results
    EudraCT Number: 2007-000202-75 Sponsor Protocol Number: P.Sitsen.03 Start Date*: 2007-06-15
    Sponsor Name:Leids Universitair Medisch Centrum
    Full Title: A comparison of the efficacy of levobupivacaine 0,125%, ropivacaine 0,125% and ropivacaine 0,2%, all combined with sufentanil 0.5 micrograms/mL, in patient-controlled epidural analgesia after hyste...
    Medical condition: Primary Objective •to compare the analgesic efficacy of levobupivacaine and ropivacaine in patient-controlled epidural analgesia, as assessed by the number of requests for epidural bolus injections...
    Disease:
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: NL (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2008-002030-30 Sponsor Protocol Number: AR_HSG_01-2008 Start Date*: 2008-04-24
    Sponsor Name:A.O. SAN GERARDO DI MONZA
    Full Title: Impact of intraperitonael nebulization of local anesthetic on hypothermia and postoperative pain associated with laparoscopic surgery
    Medical condition: Intra and post operatorive period
    Disease: Version SOC Term Classification Code Term Level
    9.1 10038604 Reproductive system and breast disorders SOC
    Population Age: Adults Gender: Female
    Trial protocol: IT (Prematurely Ended)
    Trial results: (No results available)
    EudraCT Number: 2013-003522-83 Sponsor Protocol Number: SM1-PJ-13 Start Date*: 2013-10-04
    Sponsor Name:Professor Jørgen B. Dahl
    Full Title: Adductor canal block and effect of 10 versus 30 ml ropivacaine on muscle strength: a randomized study in helathy volunteers
    Medical condition: healthy volunteers (treatment intended for postoperative pain treatment in patients after knee surgery)
    Disease: Version SOC Term Classification Code Term Level
    16.0 100000004863 10054711 Postoperative pain LLT
    Population Age: Adults Gender: Male
    Trial protocol: DK (Completed)
    Trial results: View results
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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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