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N/A
20 Years
35 Years
Not Enrolling
Female
Polycystic Ovary Syndrome

Thank you

Trial Information


Inclusion Criteria:



- PCOS (Rotterdam criteria)

- BMI < 27

- No medication for 3 months

Exclusion Criteria:

- Pregnancy

- Lactation

- Other endocrinologic disease

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Outcome Measure:

Insulin resistance

Principal Investigator

Birgitta Trolle, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

Skejby University Hospital

Authority:

Denmark: The Ministry of the Interior and Health

Study ID:

160350-2

NCT ID:

NCT00319293

Start Date:

Completion Date:

Related Keywords:

  • Polycystic Ovary Syndrome
  • Polycystic Ovary Syndrome

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