ClinicalTrials.Veeva

Menu

Prostaglandin Metabolite in Urine Samples From Patients With Ovarian Cancer

Vanderbilt University Medical Center logo

Vanderbilt University Medical Center

Status

Completed

Conditions

Ovarian Cancer

Treatments

Other: immunohistochemistry
Genetic: protein expression analysis

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT00900523
VU-VICC-IRB-060680
VU-VICC-GYN-0648
VICC GYN 0648

Details and patient eligibility

About

RATIONALE: Measuring the amount of prostaglandin metabolite in urine samples and studying tissue samples in the laboratory from patients with ovarian cancer may help doctors identify and learn more about biomarkers related to ovarian cancer and may help the study of cancer in the future.

PURPOSE: This laboratory study is measuring the amount of prostaglandin metabolite in urine samples from patients with ovarian cancer.

Full description

OBJECTIVES:

  • Determine the level of prostaglandin E_2 metabolite (PGE-M) in 24-hour urine samples collected prior to surgery or chemotherapy from patients with ovarian cancer.
  • Determine cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2) expression by western blot and immunohistochemistry (IHC) in ovarian tumor tissue samples and matched normal ovarian tissue samples, if available, from these patients.
  • Correlate urine PGE-M levels with corresponding tissue COX-1 and COX-2 levels in urine and tissue samples from these patients.

OUTLINE: This is a pilot study.

Patients submit 24-hour urine specimens prior to surgery for evaluation of urinary levels of prostaglandin E_2 metabolite (PGE-M).

Patients also undergo assessment of tissue obtained at the time of surgery, including ovarian tumor tissue, normal surface ovarian epithelium tissue (if available), and fixed tissue embedded in a paraffin block. Tissue samples are analyzed by western blot and IHC for cyclooxygenase-1 and cyclooxygenase-2 expression.

Enrollment

7 patients

Sex

Female

Ages

17+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of known or suspected ovarian cancer
  • Age greater than 17 years

Exclusion criteria

  • Pregnant or nursing
  • Taking steroids or non-steroidal anti-inflammatory drugs (NSAIDs) on a regular basis.

PRIOR CONCURRENT THERAPY:

  • No concurrent chronic use of steroids or NSAIDs

Trial design

7 participants in 1 patient group

Known or suspected ovarian cancer
Description:
Women who have a diagnosis of ovarian cancer or who are suspected of having ovarian cancer
Treatment:
Genetic: protein expression analysis
Other: immunohistochemistry

Trial contacts and locations

0

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems