Laboratory Study of Cancer & Immune Cells in Ascites Fluid of Ovarian Cancer Patients to Test Alternative Therapies

Description

Ascites samples from women undergoing surgery for ovarian cancer will be collected for use in translational research.

Conditions

Ovarian Cancer

Study Overview

Study Details

Study overview

Ascites samples from women undergoing surgery for ovarian cancer will be collected for use in translational research.

Single Institution (UNM) Prospective Laboratory Study of Cancer and Immune Cells in the Ascites Fluid of Ovarian Cancer Patients to Test Alternative Therapies

Laboratory Study of Cancer & Immune Cells in Ascites Fluid of Ovarian Cancer Patients to Test Alternative Therapies

Condition
Ovarian Cancer
Intervention / Treatment

-

Contacts and Locations

Albuquerque

University of New Mexico Cancer Center, Albuquerque, New Mexico, United States, 87131

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * All female participants, regardless of ethnicity, who are undergoing cytoreductive surgery for ovarian cancer are eligible for this study
  • * All participants will be eighteen years old or older
  • * Patients must be suspected of having a pathological diagnosis or clinical suspicion of ovarian cancer and be scheduled for surgery for tumor resection.
  • * Ability to understand and the willingness to sign a written informed consent document.
  • * Pathologic confirmation of a diagnosis of epithelial adenocarcinoma of the ovary, fallopian tube, or primary peritoneal cancer (serous, mucinous, clear cell, endometrioid, undifferentiated, mixed, transitional cell)
  • * Women of childbearing potential must have a negative qualitative serum pregnancy test ≤ 2 weeks prior to study entry.
  • * A female of child-bearing potential is any woman (regardless of sexual orientation, having undergone a tubal ligation, or remaining celibate by choice) who meets the following criteria:
  • * Has not undergone a hysterectomy or bilateral oophorectomy; or
  • * Has not been naturally postmenopausal for at least 12 consecutive months (i.e., has had menses at any time in the preceding 12 consecutive months).
  • * We do not intend to include participants if they are unable to provide informed consent for this study themselves (e.g. mentally ill patients who require health care proxies to consent for any medical intervention), or vulnerable populations such as prisoners.
  • * Minors under age eighteen.
  • * Pregnant women.
  • * Final pathologic diagnosis that does not confirm invasive epithelial ovarian, tubal, or primary peritoneal cancer

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

FEMALE

Accepts Healthy Volunteers

No

Collaborators and Investigators

New Mexico Cancer Care Alliance,

Sarah Adams, MD, PRINCIPAL_INVESTIGATOR, UNM Comprehensive Cancer Center

Study Record Dates

2027-12-31