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CYP19 Genetic Polymorphism & Aromatase Inhibitor(AI) (AI-CYP19)

K

Korea University

Status

Unknown

Conditions

Arthritis
Genetic Polymorphism
Arthralgia
Breast Neoplasms

Treatments

Drug: Aromatase Inhibitor(Femara or Arimidex)

Study type

Observational

Funder types

Other

Identifiers

NCT00973505
AN09021

Details and patient eligibility

About

The purpose of this study is to investigate the relationship between the side effects(especially arthralgia and arthritis) which appear in the patients who are prescribed aromatase inhibitor(AI) and the CYP19 genetic polymorphisms.

Enrollment

100 estimated patients

Sex

Female

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. The patient must sign the informed consent.
  2. The patient must sign the informed consent of genetic screening test.
  3. The patient must be between 18 years old and 80 years old who can make a decision independently.
  4. The patient must be post-menopause status.
  5. The patient should be the stage 1,2 or 3 of the breast cancer.
  6. The test result of the estrogen receptor or progesterone receptor is positive, so the patient should be taking the medication of AI (Aromatase Inhibitor).

Exclusion criteria

  1. The patient is pre-menopause status.
  2. The test result of serum FSH level is below 30mU/ml.
  3. The test result of the hormone receptor(ER & PR) is negative or unknown.
  4. Patient's breast cancer stage is 4 which has systemic metastatics.

Trial design

100 participants in 1 patient group

CYP19
Description:
CYP19 genetic polymorphism
Treatment:
Drug: Aromatase Inhibitor(Femara or Arimidex)

Trial contacts and locations

1

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Central trial contact

Eun Sook Lee, MD, PhD

Data sourced from clinicaltrials.gov

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