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N/A
18 Years
35 Years
Open (Enrolling)
Female
Polycystic Ovary Syndrome

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Trial Information


It is planned to compare the values ​​of FSH/LH, AMH, and 75 gr OGTT between 20 patients
diagnosed as PCOS according to the AES-Rotterdam criteria and 20 patients with multicystic
ovarian structure but do not provide the PCOS-D3 criteria. The second purpose of this study
is to investigate the mechanism that leads to the elevation of AMH in patients with PCOS,
and to reveal the effects of intraovarian paracrine factors,insulin resistance and FSH /LH.


Inclusion Criteria:



- Between the ages of 18-35

- >6 4-9 mm follicles in bilateral ovaries at ultrasonographic examination

- Increased ovarian volume (>10 ml )

Exclusion Criteria:

- Hormonal drug users

- Late onset congenital adrenal hyperplasia,androgen secreted ovarian or adrenal tumors

Type of Study:

Observational

Study Design:

Time Perspective: Prospective

Outcome Measure:

Anti-Müllerian Hormone level 0.7ng/ml -3.5ng/ml.

Outcome Description:

difference of serum AMH levels between patients with PCO or multicystic ovaries

Outcome Time Frame:

6 months

Safety Issue:

No

Authority:

United States: Institutional Review Board

Study ID:

AMH-123

NCT ID:

NCT01878955

Start Date:

April 2013

Completion Date:

August 2014

Related Keywords:

  • Polycystic Ovary Syndrome
  • Antimullarian hormone(AMH)
  • Polycystic Ovary
  • Multicystic Ovary
  • Polycystic Ovary Syndrome

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