Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
Incidence of Cancer in Women at Increased Genetic Risk of Ovarian Cancer
NCT01139957 · View on ClinicalTrials.gov ↗
Study Summary
This clinical trial is studying the incidence of cancer in women at increased genetic risk of ovarian cancer. Gathering information about genetic factors in women with an increased risk of ovarian cancer over time may help doctors learn more about the disease and find better methods of treatment and on-going care.
Conditions Studied
Interventions
- OTHER Quality-of-Life Assessment
- OTHER Questionnaire Administration
- PROCEDURE Evaluation of Cancer Risk Factors
- PROCEDURE Study of High Risk Factors
Study Locations (20)
Connecticut
- Hartford Hospital — Hartford
- Smilow Cancer Hospital Care Center at Saint Francis — Hartford
- The Hospital of Central Connecticut — New Britain
- Yale University — New Haven
Florida
- Florida Gynecologic Oncology — Fort Myers
- Mayo Clinic in Florida — Jacksonville
- Sarasota Memorial Hospital — Sarasota
- Women's Cancer Associates — St. Petersburg
Illinois
- Rush University Medical Center — Chicago
- University of Chicago Comprehensive Cancer Center — Chicago
- NorthShore University HealthSystem-Evanston Hospital — Evanston
Arizona
- Gynecologic Oncology Group of Arizona — Phoenix
- Mayo Clinic in Arizona — Scottsdale
Delaware
- Beebe Medical Center — Lewes
- Christiana Care Health System-Christiana Hospital — Newark
Alabama
- University of Alabama at Birmingham Cancer Center — Birmingham
California
- UCLA / Jonsson Comprehensive Cancer Center — Los Angeles
Colorado
- University of Colorado Hospital — Aurora
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,916 participants |
| Start Date | 2010-06-07 |
| Est. Completion | 2020-04-10 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01139957
The ClinicalTrials.gov registry entry for NCT01139957 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,916 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Gynecologic Oncology Group, which has 61 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 4 conditions, with Breast Carcinoma appearing as the primary indexed condition, and to 4 interventions — of which Quality-of-Life Assessment is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT01139957 reports 20 study locations spanning 10 distinct geographic areas — top geographies include Connecticut, Florida, Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT01139957 about?
NCT01139957 is a clinical study titled "Incidence of Cancer in Women at Increased Genetic Risk of Ovarian Cancer". This clinical trial is studying the incidence of cancer in women at increased genetic risk of ovarian cancer. Gathering information about genetic factors in women with an increased risk of ovarian cancer over time may help doctors learn more about the disease and find better methods of treatment and...
What is the current status of trial NCT01139957?
This trial is currently completed. The enrollment target is 1,916 participants. The study started on 2010-06-07. Estimated completion is 2020-04-10.
What conditions does trial NCT01139957 study?
This clinical trial studies the following conditions: Breast Carcinoma, Primary Peritoneal Carcinoma, Fallopian Tube Carcinoma, Ovarian Neoplasm. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT01139957?
The interventions under investigation include: Quality-of-Life Assessment (OTHER), Questionnaire Administration (OTHER), Evaluation of Cancer Risk Factors (PROCEDURE), Study of High Risk Factors (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT01139957?
This trial is sponsored by Gynecologic Oncology Group, which has 61 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT01139957 being conducted?
This trial has 20 study locations across Alabama, Arizona, California, Colorado, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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