Trials / Withdrawn
WithdrawnNCT00888082
Protection of Ovarian Function With Goserelin Acetate in Premenopausal Early Breast Cancer Patients With Chemotherapy
Protection of Ovarian Function With Goserelin Acetate in Premenopausal Early Breast Cancer Patients Undergoing Adjuvant Chemotherapy: An Open Label, Randomised, Multi-Centre, Phase IIIb Study
- Status
- Withdrawn
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 102 (estimated)
- Sponsor
- AstraZeneca · Industry
- Sex
- Female
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Not accepted
Summary
Primary objective of this study is to determine the effectiveness of goserelin acetate (Zoladex) in preserving ovarian function in premenopausal women undergoing adjuvant chemotherapy for primary invasive breast cancer by documenting persistence or resumption of regular menses via menstrual history, serum FSH and E2 measurements. The secondary objectives of this study are as follows: To investigate the impact of treatment with chemotherapy with or without goserelin acetate (i.e. impact of the expectation of ovarian function preservation) on participants' quality of life (QOL) by FACT-ES scale, and to compare safety and tolerability of study drugs in two treatment groups by evaluation of adverse events.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Goserelin acetate | 3.6 mg depot injectable preparation |
Timeline
- Primary completion
- 2012-04-01
- Completion
- 2012-04-01
- First posted
- 2009-04-24
- Last updated
- 2010-12-10
Locations
3 sites across 1 country: Turkey (Türkiye)
Source: ClinicalTrials.gov record NCT00888082. Inclusion in this directory is not an endorsement.