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Quality Of Life While Receiving Faslodex

Quality Of Life And Symptoms In Postmenopausal Women With Hormone Receptor Positive Disseminated Breast Cancer While Receiving Faslodex.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00643513
Enrollment
120
Registered
2008-03-26
Start date
2007-06-30
Completion date
2009-01-31
Last updated
2009-04-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

QUALITY OF LIFE, POSTMENOPAUSAL WOMEN, HORMONE RECEPTOR POSITIVE DISSEMINATED BREAST CANCER, FASLODEX

Brief summary

To study QoL related response, symptom spectrum and severity in disseminated breast cancer patients receiving Faslodex hormonal therapy.

Interventions

None listed

Sponsors

AstraZeneca
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Histologic and/or cytological proven breast cancer. * Patients with metastases of breast cancer ± postmenopausal primary tumor ≥12 months. * Positive oestrogen receptors (ER+), positive progesterone receptors (PgR+) or unknown hormonal receptors (if duration between surgery and metastasis occurring is not less 2 years) which are indirect confirmation of hormone sensitive tumor. * ECOG performance status of ≤ 2 * Patient willingness to take part in the programm * Life expectancy of more than 6 months. * Patient ability to complete a questionnaire.

Exclusion criteria

* Contraindications for Faslodex therapy * Other anticancer therapy (chemotherapy, hormonal therapy with other drugs, radiotherapy), except for radiotherapy of sites which are not only measurable or evaluable manifestation of disease.

Design outcomes

Primary

MeasureTime frame
To study QoL related response, symptom spectrum and severity in disseminated breast cancer patients receiving Faslodex hormonal therapy.

Countries

Russia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026