Last updated: February 6, 2023
Sponsor: Cairo University
Overall Status: Active - Recruiting
Phase
3
Condition
N/ATreatment
N/AClinical Study ID
NCT05637671
CL(3204)
Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Post-menopausal female patients who are 18 years of age or older.
- Patients diagnosed with hormone receptor-positive breast cancer stage 0 - IIIC (non-advanced breast cancer) who are taking aromatase inhibitors as adjuvant therapy (post-surgery) and having Significant vasomotor symptoms, defined as a mean of 5moderate to severe hot flashes per day.
- Have an Eastern Cooperative Oncology Group performance status rating (ECOG-PSR) ˂ 2.
- Life expectancy greater than 6 months.
- Normal serum creatinine level and bilirubin level is less than two times the normallevel.
- Serum follicle-stimulating hormone (FSH) levels above 40 mIU/mL.
Exclusion
Exclusion Criteria:
- Patients taking tamoxifen as adjuvant therapy.
- Metastatic breast cancer.
- Other treatments used for hot flashes, antidepressants, and monoamine oxidaseinhibitors (except if they are discontinued for at least one month before studyentry).
- Hypersensitivity to paroxetine or oxybutynin.
- Presence of a condition requiring use of an anticholinergic agent.
- Untreated hypertension.
- Impaired liver or kidney function.
- Unstable cardiac disease.
- Pregnancy or breastfeeding.
- History of self-injurious behavior.
- History of clinical diagnosis or treatment of any psychiatric disorder.
- Prior use of oxybutynin or paroxetine for hot flushes.
- Recent use of oxybutynin or paroxetine for conditions other than vasomotor symptomsunless they are stopped at least 30 days before the study entry.
Study Design
Total Participants: 146
Study Start date:
February 10, 2022
Estimated Completion Date:
December 31, 2023
Connect with a study center
Dar El-Salam Cancer Hospital
Cairo, Governorate 11617
EgyptActive - Recruiting
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