Breast Ultrasonography and Polycystic Ovary Syndrome

Sponsor
Kanuni Sultan Suleyman Training and Research Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT04231786
Collaborator
(none)
1
1
6
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Study Details

Study Description

Brief Summary

The results of the evaluation of breast ultrasonography results of patients with polycystic ovary syndrome diagnosis over 30 years of age will be evaluated.

Patients admitted to the outpatient clinic and rotterdam criteria according to laboratory data and polycystic ovary syndrome patients diagnosed by the same radiologist the next day after the end of menstrual breast ultrasonography. The aim of this study is to show the association of polycystic ovary syndrome and fibrocystic breast.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Breast ultrasonography findings

Study Design

Study Type:
Observational [Patient Registry]
Actual Enrollment :
1 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Breast Ultrasonography Findings in Patients Over 30 Years With Polycystic Ovary Syndrome
Actual Study Start Date :
Jan 14, 2020
Actual Primary Completion Date :
Jul 14, 2020
Actual Study Completion Date :
Jul 14, 2020

Outcome Measures

Primary Outcome Measures

  1. Breast ultrasonography findings [1 month]

    Breast ultrasonography findings in patients over 30 years of age diagnosed with polycystic ovary syndrome. THE PRESENCE OF FIBROCISTIC DISEASE WILL BE EVALUATED FOR FIBROADENOMA OR OTHER BREAST DISEASE. YES OR NO ; WILL BE REGISTERED.

Eligibility Criteria

Criteria

Ages Eligible for Study:
30 Years to 45 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Over 30 years

  • diagnosed with polycystic ovary syndrome according to rotterdam criteria

  • no previous history of breast disease

  • female patients

Exclusion Criteria:
  • Under 30 years

  • polycystic ovary syndrome

  • patients with a previously known history of breast disease

Contacts and Locations

Locations

Site City State Country Postal Code
1 Kanuni Sultan Süleyman Training and Research Hospital Istanbul Turkey 33404

Sponsors and Collaborators

  • Kanuni Sultan Suleyman Training and Research Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Pınar Kadirogulları, Pınar Kadiroğulları M.D, Department of Obstetrics and Gynecology,Principal Investigator, Kanuni Sultan Suleyman Training and Research Hospital
ClinicalTrials.gov Identifier:
NCT04231786
Other Study ID Numbers:
  • 2019.05.122
First Posted:
Jan 18, 2020
Last Update Posted:
Sep 3, 2020
Last Verified:
Sep 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Pınar Kadirogulları, Pınar Kadiroğulları M.D, Department of Obstetrics and Gynecology,Principal Investigator, Kanuni Sultan Suleyman Training and Research Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 3, 2020