Pubertal Induction in Individuals With Hypogonadism

Status Not yet recruiting

Clinical Trial Summary

The investigators wish to explore the variability of uterine, breast and bone outcome markers as surrogates to assess the adequacy of exogenous oestrogen replacement in individuals with hypogonadism.

Clinical Trial Description

The investigators will invite individuals with hypogonadism who require pubertal induction to participate in the study. The participants will receive conventional routine oestrogen replacement in the form of transdermal patch. The participants will be reviewed every 2 months for a total of 8 months to document uterine, breast and bone assessment. This will be completed using a variety of tools. After 4 months, the participants will receive an incremental increase in oestrogen dose. ;

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02871986
Study type	Observational
Source	University College, London
Contact	Gerard Conway, FRCP, MD
Phone	02073809101
Email	g.conway@ucl.ac.uk
Status	Not yet recruiting
Phase	N/A
Start date	September 2016
Completion date	March 2020

View Details

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