Fertility Clinical Trial
Official title:
Aromatase Inhibitor Effects on Ovarian Function During the Follicular and Early Luteal Phase in Women
A single center, open label randomized clinical trial designed to examine ovarian follicular
dynamics following attempted atresia induction during the late follicular and early luteal
phase of the menstrual cycle using an aromatase inhibitor.
We hypothesize that administration of an aromatase inhibitor (AI) at biologically important
times of the natural menstrual cycle will cause ovulatory failure in women with preovulatory
follicles and failure of luteogenesis in women who have recently ovulated. It is proposed
that atresia of the dominant follicle and formation of anovulatory structures will be
associated with arrested endometrial development and a shortened interval to menstrual
bleeding (3 days). We anticipate that this will provide us with information to facilitate
the development of a new method for emergency contraception and a greater understanding of
human folliculogenesis.
The rationale for the proposed research project is based on the ovarian synchronization
concepts developed and documented in the bovine model in the Reproductive Science and
Medicine Research group at the University of Saskatchewan combined with novel human ovarian
wave concepts of folliculogenesis first elucidated in the Women's Health Imaging Research
Laboratory (WHIRL) in the Department of Obstetrics, Gynecology and Reproductive Sciences.
In clinical practice emergency contraception (EC) intends to suppress follicular
development, ovulation, or the ability of a conceptus to implant. Exogenous steroids,
estrogen and progestin, are used in various formulations to accomplish the suppression.
Though EC are now available 'over-the-counter' in Canada and many countries around the
world; the ovarian response is unpredictable and EC do not inhibit ovulation at the most
critical times of the menstrual cycle. In 2002 approximately 120,000 of 450,000 pregnancies
in Canada ended in elective pregnancy termination. In the US 49% of the 3.5 million annual
pregnancies were unintended and 54% of the unintended pregnancies resulted in elective
termination.
Current hormonal contraceptive regimens, pre and post coital, are based on the traditional
theory of follicular development that states that a single group of antral follicles is
recruited in the late luteal phase for growth. Recent documentation has show that human
ovarian folliculogenesis occurs in a 2-3 wave like pattern during a menstrual cycle. Wave
emergence has been documented to occur in the early luteal phase with the final wave being
ovulatory. The new model of follicular wave dynamics is well established and supported by
experimental evidence in the bovine and equine models.
Traditionally these hormonal medications are taken 72 to 120 hours after known or suspected
barrier contraception failure or unprotected intercourse. The two standard steroidal EC
methods are Plan BTM, containing of 0.75 mg levonorgestrel (LNG), and the Yuzpe method,
containing 0.1 mg ethinyl estradiol (EE) and 0.5 mg LNG. Ovarian follicular development and
ovulation in women have been studied after EC use; however, the mechanisms underlying
follicular growth, regression, and ovulation during EC use remain poorly elucidated. The
mechanism of action differs with each EC regimen as well as being dependent upon the
relative timing between dosing, intercourse, and ovulation. Previous studies have shown that
EC are most effective if used when the dominant follicle diameter is small (4 to 5 days
prior to ovulation), however, during this time interval intercourse is less likely to result
in pregnancy whether or not EC were administered.
All current emergency contraception (EC) options are guided by the traditional theory of
follicular development. Based on the findings of an unpredictable response of the ovaries to
EC treatment, the occurrence of ovulation after treatment with EC, and findings of follicle
growth in a 2-3 wave pattern, we need to reconsider the phase of the menstrual cycle and the
treatment given for emergency contraception.
Aromatase inhibitors (AI) prevent the enzymatic conversion of androgens to estrogens. This
significantly lowers serum estrogen levels. AI have been administered around the time of
menses for ovulation induction and ovulation was seen to follow 10 to 12 days later. The
rationale for inducing atresia of dominant follicles stems from this observation. Acute
estradiol deprivation should theoretically initiate atresia of all viable follicles in the
cohort resulting in the emergence of a new follicle wave without an ovulation event
occurring.
;
Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science
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