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Clinical trials for Chloroprocaine

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   44336   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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    18 result(s) found for: Chloroprocaine. Displaying page 1 of 1.
    EudraCT Number: 2020-000465-17 Sponsor Protocol Number: CHL.3-02-2019 Start Date*: 2020-06-16
    Sponsor Name:Sintetica S.A.
    Full Title: A Phase II/III, Randomized, Double-Masked, Vehicle-Controlled, Efficacy, Safety and Tolerability Study of Chloroprocaine 3% Gel Eye Drops in healthy volunteers
    Medical condition: healthy volunteers
    Disease: Version SOC Term Classification Code Term Level
    20.0 10042613 - Surgical and medical procedures 10024758 Local anaesthesia PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: AT (Completed)
    Trial results: View results
    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: 2014-005469-58 Sponsor Protocol Number: AGO/2014/007 Start Date*: 2015-01-14
    Sponsor Name:Ghent University Hospital
    Full Title: Determination of the minimum local anesthetic dose (MLAD) of spinal chloroprocaine for inguinal herniorrhaphy in ambulatory surgery.
    Medical condition: Inguinal herniorrhaphy.
    Disease: Version SOC Term Classification Code Term Level
    17.1 10042613 - Surgical and medical procedures 10022020 Inguinal hernia repair PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2015-004918-22 Sponsor Protocol Number: AGO/2015/011 Start Date*: 2016-06-28
    Sponsor Name:Ghent University Hospital
    Full Title: A comparison of chloroprocaine 3% versus levobupivacaine 0.5% for epidural anesthesia during caesarean section.
    Medical condition: anesthetics for women scheduled for elective caesarean section
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2015-001944-13 Sponsor Protocol Number: ZAA15CPP Start Date*: 2016-07-27
    Sponsor Name:Zaans Medisch Centrum
    Full Title: Chloroprocaine vs prilocaine for spinal anaesthesia in day-case surgery: a double-blind randomized trial
    Medical condition: Patients scheduled for ambulatory knee arthroscopy surgery receive one of the two spinal anaesthetics
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: NL (Completed)
    Trial results: View results
    EudraCT Number: 2017-002559-27 Sponsor Protocol Number: 2017-03 Start Date*: 2018-03-29
    Sponsor Name:Zaans Medisch Centrum
    Full Title: ED50 and ED90 of intrathecal 1% chloroprocaine in day-case knee arthroscopy
    Medical condition: Patients scheduled for ambulatory knee arthroscopy surgery receive intrathecal chloroprocaine
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: NL (Completed)
    Trial results: (No results available)
    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: 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: 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: 2019-001660-30 Sponsor Protocol Number: CHL.3/01-2019/M Start Date*: 2020-06-03
    Sponsor Name:Sintetica S.A.
    Full Title: A prospective, observer-masked, randomized clinical trial to investigate and compare the clinical efficacy of chloroprocaine 3% gel and tetracaine 0.5% eye drop as topical anesthetics in phacoemuls...
    Medical condition: cataract surgery
    Disease: Version SOC Term Classification Code Term Level
    20.0 10042613 - Surgical and medical procedures 10063797 Cataract operation PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: SK (Completed) ES (Completed) IT (Completed)
    Trial results: View results
    EudraCT Number: 2016-000813-63 Sponsor Protocol Number: TACs Start Date*: 2016-04-06
    Sponsor Name:Universitair Ziekenhuis Brussel
    Full Title: Comparative doubleblind study with prilocaine 2 % and 2-chloroprocaine for elective caesarean section.
    Medical condition: Healthy pregnant women undergoing a elective caesarean section with an uncomplicated pregnancy of a singleton, "full-term", all between 18-40 y (ASAI-II) through combined spinal and epidural approach.
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2018-000656-18 Sponsor Protocol Number: 2042015 Start Date*: 2018-11-09
    Sponsor Name:SINTETICA SA
    Full Title: Randomized, multi-center, double-blind, two-armed, parallel active groups, prospective trial, to evaluate, in pediatric population undergoing 'Calcaneo stop' surgery or Inguinal hernia repair, the ...
    Medical condition: Pediatric patients undergoing surgery of flatfoot or inguinal hernia
    Disease: Version SOC Term Classification Code Term Level
    20.0 100000004865 10002325 Anesthesia local LLT
    Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 Gender: Male, Female
    Trial protocol: IT (Trial now transitioned) ES (Restarted)
    Trial results: (No results available)
    EudraCT Number: 2014-002519-40 Sponsor Protocol Number: CHL.2/01-2014/M Start Date*: 2015-08-17
    Sponsor Name:Sintetica S.A.
    Full Title: A prospective, randomised, non-inferiority study of Chloroprocaine 2% and the active control Ropivacaine 0.75% (AstraZeneca) in ultrasound-guided axillary nerve block for short-duration distal uppe...
    Medical condition: Local anaesthesia by axillary nerve block
    Disease: Version SOC Term Classification Code Term Level
    19.1 10042613 - Surgical and medical procedures 10024758 Local anaesthesia PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: AT (Completed)
    Trial results: View results
    EudraCT Number: 2016-000298-20 Sponsor Protocol Number: CHL.3/01-2016 Start Date*: 2016-10-18
    Sponsor Name:Sintetica S.A.
    Full Title: Comparison of epidural Chloroprocaine 3% and Ropivacaine 0.75% for unplanned Caesarean section in labouring women who have an epidural catheter in situ
    Medical condition: Local epidural anaesthesia in labouring women who have an epidural catheter in situ and established analgesia and need unplanned Caesarean
    Disease: Version SOC Term Classification Code Term Level
    20.0 10042613 - Surgical and medical procedures 10024758 Local anaesthesia PT
    Population Age: Adults Gender: Female
    Trial protocol: BE (Prematurely Ended) DE (Prematurely Ended) AT (Prematurely Ended)
    Trial results: View results
    EudraCT Number: 2008-003552-29 Sponsor Protocol Number: There is no commercial sponsor Start Date*: 2008-09-12
    Sponsor Name:Johannes Förster, anest.lääkäri
    Full Title: Kloroprokaiini (40 mg) ja artikaiini (60 mg) päiväkirurgisina spinaalipuudutteina (Lyhenne: C40A60)
    Medical condition: Verrataan 40 mg klooriprokaiinia (Ryhmä C40) ja 60 mg artikaiinia (Ryhmä A60) potilailla, joille on tarkoitus tehdä spinaalipuudutuksessa polven tähystys päiväkirurgisena toimenpiteenä. Hypoteesina...
    Disease: Version SOC Term Classification Code Term Level
    9.1 10054948 Meniscus operation LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: FI (Completed)
    Trial results: View results
    EudraCT Number: 2013-002815-88 Sponsor Protocol Number: BUPCHLOR1 Start Date*: 2013-08-08
    Sponsor Name:UZ Brussel
    Full Title: Randomised comparative trial of Bupivacaine and 2-Chloroprocaine by caesarean section.
    Medical condition: Healthy pregnant women undergoing a planned c-section with an uncomplicated pregnancy of a singleton, "full-term", all between the age of 18-40 y (ASAI-II).
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: BE (Completed)
    Trial results: View results
    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: 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)
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