← Eichor
Study identifier: NCT01601171 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Kallmann Syndrome · Hypogonadotropic Hypogonadism · Hypothalamic Amenorrhea  ·  Sponsor: Centre Hospitalier Universitaire Vaudois

PhaseN/A
Planned participants2000
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersYes

About this study

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

This description comes directly from the study's public registry record.

Talk to the study team

Emmanuelle Paccou  ·  +41 79 556 60 13  ·  emmanuelle.paccou@chuv.ch

Michela Adamo, MD  ·  +41 079 556 85 14  ·  michela.adamo@chuv.ch

Always discuss trial participation with your own doctor first.

Locations (1)

Centre Hospitalier Universitaire Vaudois (CHUV)Lausanne, Canton of Vaud, SwitzerlandRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT01601171