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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01117272
Other study ID # WFH-PCOS-98009
Secondary ID
Status Completed
Phase N/A
First received May 3, 2010
Last updated November 13, 2013
Start date May 2009
Est. completion date April 2010

Study information

Verified date November 2013
Source Taipei Medical University WanFang Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Polycystic ovarian syndrome (PCOS) is the most common endocrine disorder of reproductive-age women. According to Rotterdam 2003 criteria: at least two of three criteria are met, hyperandrogenism, chronic anovulation, and polycystic ovary. PCOS will cause irregular menstrual cycle, infertility, acne, hirsutism, obesity, or/and metabolic syndrome, diabetes that may increase risk of cardiovascular disease.

Hyperprolactinaemia is also a common problem in reproductive aged women. Both hyperprolactinaemia and PCOS had endocrine disorder and irregular menstrual cycle. Investigators hope to collect clinical data from PCOS and prolactinemia patients followed in Wang Fang hospital for many years in endocrinological and metabolical aspects for comparison. Investigators at the same time would like to understand more about other similarities and differences between these two endocrinological dysfunction for future study.


Recruitment information / eligibility

Status Completed
Enrollment 474
Est. completion date April 2010
Est. primary completion date February 2010
Accepts healthy volunteers No
Gender Female
Age group 15 Years to 45 Years
Eligibility Inclusion Criteria:

- PCOM by ultrasound Diagnosis

- Anovulation, Oligo menses

- Hyperandrogenism

Exclusion Criteria:

- Women who had been diagnosed with other etiology that should be excluded in PCOS diagnosis, such as hyperprolactinemia, hypogonadotropic hypogonadism, premature ovarian failure, congenital adrenal hyperplastic, androgen-secreting tumor, Cushing's syndrome, disorders of uterus( such as Asherman's syndrome, Mullerian agenesis), chromosomal anomalies( such as Turner syndrome).

- Women who did not have sufficient clinical or biochemical records.

- Girls who had menarche at <3 years of age and women who were >40 years of age.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Taiwan Taipei Medical University WanFang Hospital Taipei

Sponsors (1)

Lead Sponsor Collaborator
Taipei Medical University WanFang Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary hyperprolactin Who visited the Reproductive Endocrinology Clinic at Taipei Medical University-Wan Fang Medical Center from April 2004 to June 2007
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