Phase
Condition
N/ATreatment
N/AClinical Study ID
Ages 40-52 Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Female patients aged 40 to 52 years (inclusive) with mastodynia and BI-RADS category
The patient's written informed consent to participate in any study-related procedures.
According to the Investigator, the patient's ability to comply with all therequirements of the study protocol, i.e. the patient's ability to cooperateadequately.
Patients who do not have chronic diseases of the cardiovascular system, neuroendocrinesystem, kidneys, liver, gastrointestinal tract, respiratory system, skin in thedecompensation stage.
Consent to use reliable, evidence-based contraceptive methods (double containing thefollowing types: hormonal, barrier, intrauterine spiral, etc.) throughout the study (from the time of the Informed Consent to Visit 6) .
Exclusion
Exclusion Criteria:
Hypersensitivity to the components of the IMP.
Burdened history of allergies.
Participation in another clinical study less than 90 days before signing the informedconsent form.
History of cancer.
Pregnancy or lactation.
Administration of dopamine agonists, dopamine antagonists, oestrogens andantiestrogens, dopamine.
Secondary amenorrhoea within 6 months or more.
Surgical, pharmacological or physiological menopause (except hysterectomy).
The prolactin level is more than 80 ng/mL.
Other reasons which make the patient's participation in the study undesirable,according to the Investigator.
Study Design
Study Description
Connect with a study center
Clinical and diagnostics center
Kharkiv, 61057
UkraineActive - Recruiting
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