NCT01601171Recruiting
Genetics of Reproductive Disorders (Including Kallmann Syndrome) and Cleft Lip and/or Palate
Summary
The purpose of this study is to explore the genetic basis of reproductive disorders and cleft lip and/or palate.
Inclusion criteria
(any of the following conditions) • hypogonadotropic hypogonadism • Kallmann syndrome • adult-onset hypogonadotropic hypogonadism • hypothalamic amenorrhea • polycystic ovarian syndrome • primary gonadal failure • precocious puberty • cleft lip/palate • family members of the above groups
Exclusion criteria
• acute illness/hospitalization • pituitary tumors • iron overload (hemochromatosis) • infiltrative diseases (sarcoidosis) • chronic alcohol abuse • illicit drug use • anabolic steroid abuse
Contacts
The trial team's contact details are shown on request.
See the official trial record- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Countries
- Switzerland
- Sponsor
- Centre Hospitalier Universitaire Vaudois(Other)
- Protocol no.
- 345/11
- Conditions
- Kallmann Syndrome, Hypogonadotropic Hypogonadism, Hypothalamic Amenorrhea, Polycystic Ovarian Syndrome, Precocious Puberty, Cleft Lip and Palate, Cleft Palate, Cleft Lip
- Interventions
- —
Collaborators
Swiss National Science Foundation
Locations · 1
- Lausanne, SwitzerlandCentre Hospitalier Universitaire Vaudois (CHUV)Recruiting at this site
In total, worldwide, the only site listed in the registry is recruiting.
Site status per the ClinicalTrials.gov registry (last update posted: June 21, 2022).
This status may have changed and says nothing about your eligibility: before taking any step, check with your oncologist or the site.
See also
Other versions
These results are indicative and do not replace medical advice — discuss them with your doctor.