Status:

UNKNOWN

Evaluation of Fluciclovine Uptake in Patients With Cervical, Ovarian Epithelial or Endometrial Cancers.

Lead Sponsor:

Bital Savir-Baruch

Collaborating Sponsors:

Blue Earth Diagnostics

Conditions:

Cervical Cancer

Endometrial Cancer

Eligibility:

FEMALE

18+ years

Phase:

PHASE4

Brief Summary

An important part of staging and deciding the method of treatment is knowing areas of how cancer is involved. Diagnostic imaging is often used to determine the location of the cancer using techniques ...

Eligibility Criteria

Inclusion

  • GYN cancer (ovarian, endometrial, or cervical) was biopsy-proven and/or schedule for subsequent surgery based on clinical presentation (imaging, markers)
  • Age ≥ 18 years.
  • Can tolerate 18F-fluciclovine PET/CT exam (can lie on her back for the duration of the scan).
  • Ability to understand and the willingness to sign a written informed consent.

Exclusion

  • Ongoing systemic therapy for cancer
  • Systemic therapy for cancer in the past 3 months
  • Inability to tolerate 18F-fluciclovine PET/CT exam
  • Pregnant or lactating women

Key Trial Info

Start Date :

November 14 2018

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

December 1 2020

Estimated Enrollment :

30 Patients enrolled

Trial Details

Trial ID

NCT03349463

Start Date

November 14 2018

End Date

December 1 2020

Last Update

February 28 2020

Active Locations (1)

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Loyola University Medical Center

Maywood, Illinois, United States, 60153