Skip to main content
MedPathMedPath Home
Clinical Trials/EUCTR2009-014501-13-FR
EUCTR2009-014501-13-FR
Active, not recruiting
Not Applicable

Determination De La Dose Efficace De L-Bupivacaine Pour Rachianesthésie En Chirurgie Proctologique : Étude Comparative Prospective Randomisée En Double Aveugle. - CHIRO

Hospices Civils de Lyon0 sitesSeptember 7, 2009
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit
Conditionschirurgie ano-rectaleMedDRA version: 12.0Level: LLTClassification code 10050622Term: Anorectal operation

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
chirurgie ano-rectale
Sponsor
Hospices Civils de Lyon
Status
Active, not recruiting
Last Updated
14 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 7, 2009
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •\- les personnes âgées de 18 ans et plus
  • •\- hospitalisées pour une chirurgie proctologique
  • •\- quel que soit leur sexe
  • •\- classification ASA 1, 2 ou 3
  • •\- ne présentant pas de critères d’exclusion de l’étude
  • •\- dont le consentement éclairé écrit aura été recueilli
  • •\- patients affiliés à un régime de sécurité sociale.
  • •Are the trial subjects under 18? no
  • •Number of subjects for this age range:
  • •F.1\.2 Adults (18\-64 years) yes

Exclusion Criteria

  • •\- âge \< 18 ans
  • •\- taille inférieure à 150cm ou supérieure à 190cm
  • •\- classification ASA 4 ou 5
  • •\- contre\-indication à la réalisation d’une rachianesthésie :
  • •\- allergie connue aux anesthésiques locaux,
  • •\- patients bénéficiant d’un traitement par clopidogrel ne pouvant être interrompu
  • •\- infection ou lésion au site de ponction
  • •\- trouble de l’hémostase (TP \< 50 %, TCA \> 1,5 témoin, plaquettes \< 100 G/L)
  • •\- hyperthermie supérieure à 38°C
  • •\- affection neurologique démyélinisante évolutive

Outcomes

Primary Outcomes

Not specified

Similar Trials

Active, not recruiting
Not Applicable
Evaluation of pharmacokinetics of levobupivacaine and ropivacaine during epidural infusion - NDMajor surgeryMedDRA version: 9.1Level: SOCClassification code 10042613
EUCTR2010-019393-32-ITOSPEDALE POLICLINICO S. MATTEO
Completed
Phase 4
Optimal Bupivacaine Dose for Initiation of Labor Epidural TechniquesLabor PainAnalgesia
NCT04814537Brigham and Women's Hospital100
Not yet recruiting
Not Applicable
Assessing the appropriate dose and efficacy of bovine lactoferrin to correct iron deficiency anaemia in non pregnant women: A community-based randomized controlled trial in Mirpur, DhakaIron Deficiency Anemia
ACTRN12617001455358International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b)556
Not yet recruiting
Not Applicable
Assessing the appropriate dose and efficacy of bovine lactoferrin to correct iron deficiency anaemia in pregnancy: A community-based randomized controlled trial in Mirpur, DhakaIron Deficiency Anemia
ACTRN12617001634369International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b)608
Not yet recruiting
Phase 4
Study to compare Bupivacaine heavy, Levobupivacaine plain and Levobupivacaine heavy with Fentanyl (opioid) as an add on drug under spinal anesthesia in Prostate surgery.Health Condition 1: N401- Benign prostatic hyperplasia withlower urinary tract symptoms
CTRI/2023/06/054367Dr Sanyukta Paul