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Clinical Trials/EUCTR2009-009114-40-FR
EUCTR2009-009114-40-FR
Active, not recruiting
Not Applicable

Impact de la technique anesthésique et analgésique sur le risque de récidive biologique de cancer de la prostate - Péri-Prostate

Hopital Foch0 sitesMarch 25, 2009
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Conditionsprostate cancerMedDRA version: 9.1Level: LLTClassification code 10060862Term: Prostate cancer
DrugsNaropeine 2 mg/ml solution injectable en pochePropofolUltivaMorphineNaropeine 7.5 mg/ml solution injectable en ampoule

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
prostate cancer
Sponsor
Hopital Foch
Status
Active, not recruiting
Last Updated
14 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 25, 2009
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
Male

Investigators

Eligibility Criteria

Inclusion Criteria

  • •\- Age \> 75 years
  • •\- Radical prostatectomy
  • •\- Gleason score \<9
  • •\- PSA \< 20 ng/ml
  • •\- Cancer Stage \< T3
  • •Are the trial subjects under 18? no
  • •Number of subjects for this age range:
  • •F.1\.2 Adults (18\-64 years) yes
  • •F.1\.2\.1 Number of subjects for this age range
  • •F.1\.3 Elderly (\>\=65 years) yes

Exclusion Criteria

  • •\- Age lower than 18 years,
  • •\- Allergy to propofol, peanut or soya, remifentanil, morphine, muscle relaxant, or to a component,
  • •\- History of hypersensibility to remifentanil or to a derivate of fentanyl,
  • •\- Patients receiving a psychotropic treatment, and patients taking agonist\-antagonist opiates,
  • •\- Presence of a central neurological disorder or a lesion cerebral,
  • •\- Contra\-indication to an epidural anesthesia

Outcomes

Primary Outcomes

Not specified

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