RecruitingNCT01601171

Genetics of Reproductive Disorders (Including Kallmann Syndrome) and Cleft Lip and/or Palate

The Genetics of Neuroendocrine Reproductive Disorders and of the Cleft Lip and/or Palate


Sponsor

Centre Hospitalier Universitaire Vaudois

Enrollment

2,000 participants

Start Date

Mar 1, 2012

Study Type

OBSERVATIONAL

Conditions

Summary

The purpose of this study is to explore the genetic basis of reproductive disorders and cleft lip and/or palate.


Eligibility

Plain Language Summary

Simplified for easier understanding

This study is investigating the genetic causes of reproductive and hormonal disorders — including conditions where puberty does not develop normally, irregular menstrual cycles, polycystic ovaries, and cleft lip or palate — to better understand how genes influence these conditions. **You may be eligible if...** - You have one of the following conditions: hypogonadotropic hypogonadism (the body does not produce enough sex hormones), Kallmann syndrome (a condition combining lack of puberty with a reduced sense of smell), hypothalamic amenorrhea (missed periods due to a hormonal imbalance), polycystic ovarian syndrome (PCOS), premature ovarian failure, early puberty, or cleft lip or palate - You are a family member of someone with one of the above conditions **You may NOT be eligible if...** - You are currently acutely ill or hospitalized - You have a pituitary tumor, iron overload (hemochromatosis), sarcoidosis, chronic alcohol abuse, or illicit drug use - You have other medical conditions that could explain your hormone or reproductive symptoms Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(1)

Centre Hospitalier Universitaire Vaudois (CHUV)

Lausanne, Canton of Vaud, Switzerland

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NCT01601171


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