Overview

Relative Desirability of Metformin vs. Birth Control Pill in Treating PCOS in Women of Later Reproductive Age

Status:
Recruiting
Trial end date:
2024-04-30
Target enrollment:
0
Participant gender:
Female
Summary
The goal of this study is to determine the relative desirability of metformin vs. oral combined hormonal contraceptives (OCs) in treating Polycystic Ovary Syndrome (PCOS) in women of later reproductive age. Polycystic Ovary Syndrome Questionnaire (PCOSQ) score will be used as a proxy for patient satisfaction. In light of their respective effects on the classic and metabolic facets of PCOS, metformin will provide non-inferior patient satisfaction compared to OCs in later reproductive age women with PCOS.
Phase:
Early Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
University of Virginia
Treatments:
Contraceptive Agents
Contraceptives, Oral
Contraceptives, Oral, Combined
Estradiol
Ethinyl Estradiol
Metformin
Norethindrone
Norethindrone Acetate
Criteria
Inclusion Criteria:

- Women with PCOS aged 40-49 years. Subject is considered to have PCOS if she has
current or verifiable history of: a) clinical and/or biochemical evidence of
hyperandrogenism plus b) oligomenorrhea or irregular menstruation (substantially
inconsistent menstrual cycle length). Subjects with fewer than 10 menses/year or
average menstrual cycle length >35 days are allowed to participate if they have a
compelling past history of oligomenorrhea (average menstrual cycle length >45 days or
fewer than 9 menses/year) or irregular menstruation.

- Screening safety labs within normal reference ranges although mild abnormalities that
are common in obesity and/or hyperandrogenism will not be grounds for exclusion (see
exclusion criteria).

- Subjects must be willing and able to provide written informed consent.

- Willingness to strictly avoid pregnancy (using non-hormonal methods) during the time
of the study

- Willingness and ability to comply with scheduled visits and study procedures

Exclusion Criteria:

- Postmenopausal status (i.e., absence of periods for previous year plus elevated
follicle stimulating hormone [FSH] level)

- Biochemical evidence for perimenopause as defined by an anti-Mullerian hormone <0.5
ng/mL. As an alternative, cycle day 3 FSH > 9 IU/L (with concomitant estradiol level
>80 pg/mL), if this testing is available, will serve as evidence of perimenopause
status. NOTE: If FSH >9 IU/L on screening (but it is not cycle day 3), FSH and
estradiol will be repeated on cycle day 3

- History of hysterectomy and/or bilateral oophorectomy

- BMI ≥ 40 kg/m2

- Inability to comprehend what will be done during the study or why it will be done.

- Being a study of older women with PCOS, children and men will be excluded.

- Pregnancy or lactation within the past 6 months. Subjects with a positive pregnancy
test will be informed of the result by the screening physician.

- Prisoners.

- History of (or clinical evidence for) Cushing's syndrome or adrenal insufficiency.

- History of congenital adrenal hyperplasia or 17-hydroxyprogesterone (17-OHP) >200
ng/dL, which suggest the possibility of congenital adrenal hyperplasia. 17-OHP will be
collected during follicular phase. NOTE: if a 17-OHP >200 ng/dL and is confirmed on
repeat testing, an ACTH-stimulated 17-OHP <1000 ng/dL will be required for study
participation.

- Total testosterone >150 ng/dL, which suggests the possibility of virilizing neoplasm.

- DHEA-S greater than 1.5 times the upper limit of normal range (mild elevations may be
seen in PCOS, so elevations < 1.5 times the upper limit of normal will be accepted in
these groups).

- Virilization

- Diagnosis of diabetes mellitus (DM), fasting glucose ≥ 126 mg/dL, or a hemoglobin A1c
of ≥ 6.5%.

- Abnormal thyroid stimulating hormone (TSH). Subjects with stable and
adequately-treated hypothyroidism, reflected by normal TSH values, will not be
excluded.

- Moderate to severe hyperprolactinemia. Mild prolactin elevations may be seen in PCOS,
and elevations < 1.5 times the upper limit of normal will be accepted in this group.

- Persistent liver abnormalities, with the exception that mild bilirubin elevations will
be accepted in the setting of known Gilbert's syndrome. Mild transaminase elevations
may be seen in women with obesity, so elevations <1.5 times the upper limit of normal
will be accepted in this group.

- Persistent hematocrit <36% and hemoglobin <12 g/dL.

- Abnormal sodium, potassium, or bicarbonate concentrations or elevated creatinine
concentration.

- Significant history of pulmonary dysfunction (e.g., asthma or COPD requiring
intermittent systemic corticosteroid, pulmonary hypertension, etc.).

- History of known or suspected congestive heart failure.

- History of known or suspected ischemic heart disease or cerebrovascular disease.

- History of hypertension.

- History of uncontrolled/untreated dyslipidemia. Subjects with stable and adequately
treated dyslipidemia reflected by normal lipid panel values will not be excluded.

- History of complicated valvular heart disease (e.g. pulmonary hypertension, risk of
atrial fibrillation, history of subacute bacterial endocarditis)

- History of stroke

- History of smoking

- History of severe cirrhosis or liver tumor (e.g. hepatocellular adenoma or malignant
hepatoma).

- Use of anticonvulsants, rifampicin or rifabutin therapy. The interaction of these
drugs with OCs will not be harmful to the subjects, but it will reduce the
effectiveness of OCs.

- History of venous thromboembolism (e.g. deep venous thrombosis (DVT), pulmonary
embolism (PE)).

- Personal history of blood clotting disorders (e.g., protein C, protein S, positive
antiphospholipid antibodies).

- First-degree relative history of blood clotting disorder, unless the same disorder has
been formally excluded for the study subject.

- History of migraine headaches.

- History of breast, ovarian, or endometrial cancer.

- Note: If endometrial thickness on transvaginal ultrasound is >8 mm in the
proliferative (follicular) phase or >14 mm in the secretory (luteal) phase, the
subject will be referred to a gynecologist for further evaluation (38). These
particular subjects will be required to obtain a clearance from their gynecologist to
participate in this study.

- Note: Any abnormal labs may be repeated to exclude a lab error.

- No medications known to affect the reproductive system can be taken in the 2 months
prior to screening and in the 3 months prior to the study. Such medications include
oral contraceptive pills, metformin, progestins, glucocorticoids, anti-psychotics,
and/or mood stabilizers that are known to cause hormone abnormalities.