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Changes in Breast 3D Ultrasound Measurements Using Toremifene

S

Satakunta Central Hospital

Status and phase

Completed
Phase 3

Conditions

Circulatory; Change

Treatments

Drug: Toremifene

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

To investigate if there are detectable changes in volume and circulation in breasts of healthy volunteers using toremifene 20 mg in luteal phase of the menstruation cycle versus nonmedicated cycle.

Full description

20 women were participated to this trial.

Enrollment

20 patients

Sex

Female

Ages

25 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • age 25-45 healthy person
  • regular menstrual cycles
  • safe contraception(for example sterilization or condom)

Exclusion criteria

  • gynecological or other type of cancer
  • hormonal contraception
  • pregnancy

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

Toremifene
Other group
Treatment:
Drug: Toremifene

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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