Quality of Life in Postmenopausal Women Who Are Receiving Either Exemestane or Anastrozole With or Without Celecoxib for Stage I, Stage II, or Stage IIIA Primary Breast Cancer

NCT00090974 · Status: COMPLETED · Type: OBSERVATIONAL

Last updated 2023-06-15

No results posted yet for this study

Summary

RATIONALE: Quality-of-life assessment in postmenopausal women who are receiving hormone therapy for breast cancer may help to determine the effects of treatment on these patients and may improve the quality of life for future breast cancer patients.

PURPOSE: This clinical trial is studying quality of life of postmenopausal women who are receiving either exemestane or anastrozole with or without celecoxib for stage I, stage II, or stage IIIA primary breast cancer.

Conditions

Interventions

PROCEDURE

quality-of-life assessment

Sponsors & Collaborators

  • National Cancer Institute (NCI)

    collaborator NIH
  • NCIC Clinical Trials Group

    collaborator NETWORK
  • Eastern Cooperative Oncology Group

    lead NETWORK

Principal Investigators

  • Lynne Wagner, MD · Robert H. Lurie Cancer Center

  • Paul E. Goss, MD, PhD · Massachusetts General Hospital

Eligibility

Min Age
0 Years
Max Age
120 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-01-26
Primary Completion
2013-01-30
Completion
2013-01-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00090974 on ClinicalTrials.gov