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Clinical Trials/EUCTR2008-005436-33-FR
EUCTR2008-005436-33-FR
Active, not recruiting
Not Applicable

Apport de l’échographie doppler avec injection de contraste pour la prise en charge des cancers du col de l’utérus de stade IB et II traités par radiochimiothérapie concomitante - SONOCO

CHRU de TOURS0 sitesNovember 6, 2008
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ConditionsCancer du col de l'utérus épidermoïde ou adénocarcinome, de stade IB et IIA > à 4 cm ou IIB proximalMedDRA version: 9.1Level: LLTClassification code 10008364Term: Cervix uteri cancer stage IMedDRA version: 9.1Level: LLTClassification code 10008365Term: Cervix uteri cancer stage II
DrugsSONOVUE

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cancer du col de l'utérus épidermoïde ou adénocarcinome, de stade IB et IIA > à 4 cm ou IIB proximal
Sponsor
CHRU de TOURS
Status
Active, not recruiting
Last Updated
14 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
November 6, 2008
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Diagnostic de cancer du col épidermoïde ou adénocarcinome posé sur une biopsie, de stade IB et IIA de plus de 4 cm ou IIB proximal. Il sera indispensable que le plan de traitement comporte un examen sous anesthésie générale et une stadification selon la classification FIGO clinique et par IRM ou TDM ou TEP Scan
  • •Patientes devant bénéficier d’une RCC comme traitement initial de la prise en charge de sa tumeur (hors curage ganglionnaire) suivie d’une curiethérapie et d’une chirurgie radicale.
  • •Signature du consentement libre et éclairé
  • •Affiliation 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
  • •F.1\.2\.1 Number of subjects for this age range
  • •F.1\.3 Elderly (\>\=65 years) yes
  • •F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • •Toute affection médicale sévère non contrôlée
  • •Masse utérine intracavitaire évocatrice de polype ou de cancer de l’endomètre
  • •Contre\-indication au produit de contraste

Outcomes

Primary Outcomes

Not specified

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