Plasma progesterone and plasma estradiol levels are commonly used to m
onitor ovulation in women although for the adequate documentation of o
vulation the expense and discomfort of multiple venipuncture sampling
may be required. Accurate and definitive information on ovulation in w
omen can be obtained by the simple measurement of metabolites of proge
sterone and estradiol in early morning urine samples. These analyses h
ave been made possible by the use of our own highly specific monoclona
l antibodies to both pregnanediol-3-glucuronide (P-3-G) and estrone-3-
glucuronide (E-3-G) and the development of simple, direct, automated e
nzyme-linked immunosorbent assays. Sequential sampling and the generat
ion of ovulation profiles allows detection of ovulation and identifica
tion of the infertile/fertile phases of the cycle for either planned p
regnancies or natural family planning. Aberrations in ovulation are ea
sily defected as is documentation of the transition to menopause. The
use of sequential, spaced, early morning urine samples for P-3-G and E
-3-G allows accurate assessment of ovulatory function rather than rely
ing on the usual single plasma sampling. The data presented also show
that the direct determination of plasma pregnanediol-3-glucuronide in
plasma is as informative as plasma progesterone measurement.