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NCT03943316Recruiting

Prospective Laboratory Study Biologic Specimens and Tumor Tissue of Patients With Cancer

Single Institution (UNM) Prospective Laboratory Study Biologic Specimens and Tumor Tissue of Patients With Cancer

Source: ClinicalTrials.gov · Last updated 18 Sept 2026

Brief summary (registry, in English)

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

Status (registry)
Recruiting
Study type
Observational
Enrollment
500 (estimated)
First submitted
7 May 2019
Start date
2 Dec 2015
Primary completion date
31 Dec 2030
Lead sponsor
New Mexico Cancer Research Alliance
NCT number
NCT03943316

What you commit to

  • Study type: Observational
  • Planned participants: 500
  • From 2 Dec 2015 to the primary completion date, 31 Dec 2030
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Final pathologic diagnosis that does not confirm invasive epithelial ovarian, tubal, or primary peritoneal cancer

Age

  • Minors under age eighteen.

Other

  • 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.
  • Pregnant women.

Who the study is looking for

  • 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).

Age in the registry: 18 years to - · Sex: Female

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of New Mexico Cancer Center
Coordinator of this site? Confirm its status
AlbuquerqueUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.