Clinical Study

Evaluating the Efficacy of Treatment with a GnRH Analogue in Patients with Central Precocious Puberty

Table 4

The distribution of the patients without HPG axis suppression according to subgroups () (%).

Treatment
duration
CPP ()RP-PP ()AP ()

3rd month 2 (9.5%)2 (9.5%)5 (25%)
6th month 1 (5%)04 (20%)
9th month 003 (15%)
12th month000

CPP: central precocious puberty, RP-PP: rapidly progressive precocious puberty, and AP: advanced puberty.