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Clinical Trials/EUCTR2011-001429-25-NL
EUCTR2011-001429-25-NL
Active, not recruiting
Not Applicable

Feasibility Study: FES-PET to determine ER-expression in epithelial ovarian cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
niversity Medical Center Groningen
Status
Active, not recruiting
Last Updated
14 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 16, 2011
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\.Histological evidence or high clinical suspicion with proven malignant ascites and high probability of epithelial ovarian cancer
  • 2\.The presence of at least one measurable lesion (RECIST v1\.1\).
  • 3\.Histology or cytology can be obtained (may be ascites)
  • 4\.ECOG performance status 0\-2\.
  • 5\.Postmenopausal status (defined as either \>45 years with amenorrhea \>12 months, or prior bilateral ovariectomy)
  • 6\.No history of other ER\-positive malignancies
  • 7\.Signed written informed consent
  • 8\.Able to comply with the protocol
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0

Exclusion Criteria

  • 1\.Use of estrogen receptor ligands, including tamoxifen, fulvestrant or estrogens, during the 5 weeks before entry into the study
  • 2\.Life\-expectancy \= 3 months

Outcomes

Primary Outcomes

Not specified

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