Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00086567 · ClinicalTrials.gov registry record

Predictors of Relapse of Ovarian, Peritoneal, and Fallopian Tube Cancers

A clinical trial, sponsored by National Cancer Institute (NCI).

Completed
Registry status
119
Enrollment target

NCT00086567: Completed study, sponsored by National Cancer Institute (NCI).

NCT00086567 is a clinical trial that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 119 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add start date to calendar (.ics) →

The verdict

NCT00086567 has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
119 participants
Enrollment target

Study Summary

This study will develop a blood test that can be used to predict a relapse of ovarian, peritoneal, or fallopian tube cancer. The type of testing is called proteomics, or the study of proteins in living cells. The test will identify certain proteins that might represent a pattern, or "fingerprint," indicating increased risk of disease relapse. Women with Stage III or IV epithelial ovarian cancer, primary peritoneal cancer, or fallopian tube cancer that is in remission may be eligible for this study. Candidates are screened with a medical history and physical examination, blood tests, review of pathology report from surgery, and computed tomography (CT) or magnetic resonance imaging (MRI) scans of the abdomen and pelvis (and chest if the cancer spread to the chest). Participants have a clinic visit every 3 months for a physical examination (including a pelvic examination), blood draw for routine and research tests, and review of how they have been feeling. Every 6 months they have CT scans of the abdomen, pelvis, and possibly the chest. When a patient has been in remission for 4 years, blood draws are done every 6 months and CT scans are done yearly. Patients whose cancer returns (based on a CA-125 blood test, CT scans, or physical examination) end their participation in the study. Patients with an abnormal CT scan or physical examination may be asked to undergo a tumor biopsy (surgical removal of a piece of tumor tissue) for research purposes.

Primary Outcome

Multi-institutional repository from which investigations of serum proteomic signature profiles of epithelial ovarian cancer and relapse will be developed and validated

Trial Details

FieldValue
Enrollment Target 119 participants
Start Date 2005-12-12
National Cancer Institute (NCI)

3,257 total trials

What the finished NCT00086567 record still lists

NCT00086567 is an observational study that tracks outcomes without assigning an intervention. The registered 119 participants enrollment target is mid-sized for trials with a published cap.

The record links to 0 conditions, and to 0 interventions.

NCT00086567 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00086567 about?

NCT00086567 is a clinical study titled "Predictors of Relapse of Ovarian, Peritoneal, and Fallopian Tube Cancers". This study will develop a blood test that can be used to predict a relapse of ovarian, peritoneal, or fallopian tube cancer. The type of testing is called proteomics, or the study of proteins in living cells. The test will identify certain proteins that might represent a pattern, or "fingerprint," i...

What is the current status of trial NCT00086567?

This trial is currently completed. The enrollment target is 119 participants. The study started on 2005-12-12.

Who is sponsoring clinical trial NCT00086567?

This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT04870762 · 119 participants · Phase 2

    Customized 3D Printed Oral Stents During Head and Neck Radiotherapy

  • NCT05559853 · 119 participants

    Developing a New MRI Technique to Understand Changes in Brain Tumors After Treatment

  • NCT06564389 · 119 participants · Phase 1

    FIH Study to Evaluate the Tolerability of PF-07832837 in Healthy Adults and Patients

  • NCT06742801 · 119 participants · NA

    Onyx™ Liquid Embolic IDE Clinical Study

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT00086567, the US trial registry maintained by the National Library of Medicine. NCT00086567 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.