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This trial is complete. It is no longer accepting participants. Results may be available on ClinicalTrials.gov.

NCT00987649

NCT00987649
Completed Not Applicable

Who may be able to join

Who might be able to join this trial:

  • You are a woman aged 18 or older
  • You have a mass (a growth or lump) near your ovaries or in your pelvic area, confirmed by an imaging scan such as an ultrasound
  • You are already scheduled to have surgery because of this mass (which may be a simple, complex, or solid cyst, or any similar growth in the pelvic area)
  • You are able to understand the study information and are willing to sign a consent form agreeing to take part

Who may not be able to join:

  • You have previously been diagnosed with ovarian cancer
  • You have previously had both of your ovaries removed
  • You are currently pregnant
  • You are unable to understand or sign the consent form agreeing to take part

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

Trial details

Status
Completed
Phase
Not Applicable
Sponsor
Fujirebio Diagnostics, Inc.
Registry
clinicaltrials_gov
Start date
1 October 2009
Est. completion
1 August 2010

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

1. A statistically higher number of cancer patients are correctly assigned by the combination of Initial Cancer Risk assessment and positive ROMA test result than by Initial Cancer Risk assessment alone

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

View original record on ClinicalTrials.gov