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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05866068
Other study ID # Womans
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date July 1, 2023
Est. completion date October 31, 2024

Study information

Verified date May 2023
Source Woman's
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In vitro fertilization (IVF) has helped countless couples conceive where they otherwise were unable, but does come at a significant cost. A large portion of that cost is in the medications that allow for controlled ovarian hyperstimulation. One aspect of treatment is in ovulation inhibition to allow for supraphysiologic recruitment of oocytes prior to natural ovulation. Historically, GnRH agonist and antagonists have been used. However, these are subcutaneous injections and can be costly. Clomiphene citrate is a selective estrogen receptor modulator that acts as an estrogen antagonist in the hypothalamus and pituitary and is an inexpensive oral agent. It may be used as an inhibitor of ovulation in IVF in theory but this has never been attempted to the best of our knowledge.


Description:

In vitro fertilization (IVF) has been used for over 40 years in treating infertility, and with the advent of cryopreservation, it is now possible to stimulate, retrieve and freeze oocytes for use at a later date. In fact, in late 2012 the FDA removed the experimental label from oocyte cryopreservation (OC), allowing for OC cycles to become a standard of care for patients with conditions that threaten their ovarian reserve or patients who wish to preserve their fertility electively. Currently, standard stimulation protocols for superovulation of oocytes for OC involve subcutaneous injections of GnRH agonists or antagonists to inhibit premature natural ovulation as the higher number of oocytes are recruited with gonadotropins. These medications are costly and cumbersome and therefore it is of interest to design protocols that are both easier on patient compliance and more cost effective. Clomiphene citrate is a selective estrogen receptor modulator (SERM). It selectively binds to estrogen receptors in the hypothalamus, pituitary, ovary, endometrium, and cervix producing estrogenic and anti-estrogenic effects. However the exact mechanism of clomid is poorly understood. Multiple studies have been done through animal models. One studied showed that it inhibits the negative feedback of endogenous estrogen to subsequently increase secretion of GnRH. It is also shown to increase the frequency of GnRH, however not the amplitude [Wallach]. Current IVF protocols use either GnRH antagonist or agonist to inhibit premature ovulation. Therefore due to Clomid effect on both the hypothalamus and pituitary it could theoretically block ovulation if taken continuously to down regulate the GnRH receptors. A study published in 1982 by Marut and Hodgen looked at the effect of high doses clomiphene in primates with normal cycles. Using high dose clomiphene (25mg daily) for five days then evaluated gonadotropins, estrogen, progesterone and preformed serial laparoscopies. In all 18 of the treatment cycles there was a delay in ovulation. Upon literature review, no other studies had been conducted looking using clomiphene citrate as a medication to inhibit ovulation during an ovarian stimulation cycle.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 10
Est. completion date October 31, 2024
Est. primary completion date June 30, 2024
Accepts healthy volunteers
Gender Female
Age group 18 Years to 42 Years
Eligibility Inclusion Criteria: - Female - 18-42 years old, inclusive - Planning to undergo IVF with egg retrieval for oocyte cryopreservation Exclusion Criteria: - Tobacco or illicit drug use - History of infertility - Prior failed IVF or OC cycle - Drug allergy to Clomid - Hypertension - Migraine with aura

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Clomiphene
Clomiphene citrate 100mg daily during IVF stimulation

Locations

Country Name City State
United States Womans Hospital Baton Rouge Louisiana

Sponsors (1)

Lead Sponsor Collaborator
Neil Chappell

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ovulation Evidence of premature ovulation during IVF stimulation 3 weeks
Secondary Oocyte yield Number of oocytes from IVF cycle 3 weeks
Secondary Maturity Rate % of eggs mature / # of oocytes collected 3 weeks
Secondary Side effects Number of patients reporting side effects of medication 3 weeks
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