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COMPLETED

Correlation of Menstrual Cycle Phase at Time of Primary Surgery With 5-Year Disease-Free Survival in Women With Stage I or Stage II Breast Cancer

NCT00002762 · View on ClinicalTrials.gov ↗

Study Summary

RATIONALE: Timing of breast cancer surgery may improve effectiveness of treatment and may help patients live longer. PURPOSE: Clinical trial to determine whether timing of primary surgery in relation to menstrual cycle is associated with disease-free survival 5 years after surgery in women who have stage I or stage II breast cancer.

Interventions

  • BEHAVIORAL patient interviewing to obtain menstrual history
  • PROCEDURE blood sampling

Study Locations (20)

California

  • Scripps Cancer Center at Scripps Clinic — La Jolla
  • Rebecca and John Moores UCSD Cancer Center — La Jolla

Florida

  • Baptist Regional Cancer Institute - Jacksonville — Jacksonville
  • CCOP - Mount Sinai Medical Center — Miami Beach

Georgia

  • Winship Cancer Institute of Emory University — Atlanta
  • CCOP - Atlanta Regional — Atlanta

Illinois

  • CCOP - Evanston — Evanston
  • Rockford Clinic — Rockford

Maryland

  • Franklin Square Hospital Center — Baltimore
  • Warren Grant Magnuson Clinical Center — Bethesda

Massachusetts

  • Cancer Research Center at Boston Medical Center — Boston
  • Lahey Clinic Medical Center - Burlington — Burlington

Alabama

  • MBCCOP - Gulf Coast — Mobile

Arizona

  • CCOP - Western Regional, Arizona — Phoenix

Trial Details

FieldValue
Enrollment Target 1,118 participants
Start Date 1996-06
Est. Completion 2009-10

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00002762

The ClinicalTrials.gov registry entry for NCT00002762 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 1,118 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Alliance for Clinical Trials in Oncology, which has 147 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Breast Cancer appearing as the primary indexed condition, and to 2 interventions — of which patient interviewing to obtain menstrual history 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: NCT00002762 reports 20 study locations spanning 14 distinct geographic areas — top geographies include California, Florida, Georgia. 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 NCT00002762 about?

NCT00002762 is a clinical study titled "Correlation of Menstrual Cycle Phase at Time of Primary Surgery With 5-Year Disease-Free Survival in Women With Stage I or Stage II Breast Cancer". RATIONALE: Timing of breast cancer surgery may improve effectiveness of treatment and may help patients live longer. PURPOSE: Clinical trial to determine whether timing of primary surgery in relation to menstrual cycle is associated with disease-free survival 5 years after surgery in women who have...

What is the current status of trial NCT00002762?

This trial is currently completed. The enrollment target is 1,118 participants. The study started on 1996-06. Estimated completion is 2009-10.

What conditions does trial NCT00002762 study?

This clinical trial studies the following conditions: Breast Cancer, Perioperative/Postoperative Complications. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00002762?

The interventions under investigation include: patient interviewing to obtain menstrual history (BEHAVIORAL), blood sampling (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00002762?

This trial is sponsored by Alliance for Clinical Trials in Oncology, which has 147 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00002762 being conducted?

This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial