Polycystic Ovary Syndrome, Pregnancy
Conditions
Keywords
Polycystic Ovary Syndrome, Infertility, Pregnancy, Women
Brief summary
The primary research hypothesis is that ovulation induction with an aromatase inhibitor (letrozole) is more likely to result in live birth than ovulation induction with a selective estrogen receptor modulator (clomiphene citrate) in infertile women with PCOS. A safety hypothesis will also be incorporated into the primary research hypothesis in which we hypothesize both treatments are equally safe for mother and child. Secondary research hypotheses include: 1. Treatment with letrozole is more likely to result in singleton pregnancy compared to treatment with clomiphene citrate. Singleton pregnancy is defined as presence of a single intrauterine gestational sac with a single fetal pole and observable heart motion. 2. Treatment with letrozole will less likely result in a first trimester intrauterine fetal demise than treatment with clomiphene citrate. A first trimester IUFD is defined as a pregnancy that ends before 13 weeks gestation. 3. Treatment with letrozole is more likely to result in ovulation (increased ovulation rate) compared to treatment with clomiphene citrate. Ovulation is defined as a midluteal progesterone level ≥ 3 ng/mL. 4. The shortest time to pregnancy will be with letrozole. 5. Age, body mass index, SHBG, testosterone, LH, Anti-Mullerian Hormone (AMH), and degree of hirsutism and acne will be significant predictors of ovulation and conception regardless of treatment. 6. Improvement in SHBG, testosterone, AMH, and LH levels will be significant predictors of ovulation and conception regardless of treatment. 7. DNA polymorphisms in estrogen action genes will predict response to study drug. 8. Quality of Life will be better on letrozole than clomiphene. 9. Letrozole will be more cost effective at achieving singleton pregnancies than clomiphene.
Detailed description
Preliminary data are promising for the use of letrozole to induce ovulation in infertile women with PCOS. However the true magnitude of the effect of letrozole is difficult to discern from prior studies. Therefore we intend to determine the safety and efficacy of letrozole, an aromatase inhibitor, compared to clomiphene citrate, a selective estrogen receptor modulator, in achieving live birth in infertile women with PCOS. Treatment- After progestin withdrawal, 750 women will be equally randomized to two different treatment arms: A) clomiphene citrate 50 mg every day for 5 days (day 3-7 of cycle), or B) letrozole 2.5 mg every day for 5 days (day 3-7 of cycle), for a total of 5 cycles or 20 weeks. Dose will be increased in subsequent cycles in both treatment groups for non-response or poor ovulatory response up to a maximum of 150 mg of clomiphene a day (x 5 days) or 7.5 mg of letrozole a day (x 5 days). Statistical Analysis- The primary analysis will use an intent-to-treat approach to examine differences in the live birth rate in the two treatment arms. Anticipated time to completion- A total of 4 years will be required to complete the study after start up; 31 month enrollment period, 5 month treatment period, with 9 month additional observation to determine pregnancy outcomes. This will be accomplished by enrolling \ 3.45 women with PCOS per center per month over the enrollment period (N = 7 RMN sites).
Interventions
Clomiphene citrate 50 mg every day for 5 days (day 3-7 of cycle), for a total of 5 cycles or 20 weeks
Letrozole 2.5 mg every day for 5 days (day 3-7 of cycle), for a total of 5 cycles or 20 weeks
Sponsors
Study design
Eligibility
Inclusion criteria
Key Inclusion Criteria (Must have ovulatory dysfunction and either hyperandrogenism or PCO) 1. Chronic anovulation or oligomenorrhea: defined as spontaneous intermenstrual periods of ≥45 days or a total of ≤8 menses per year, or for women with suspected anovulatory bleeding, a midluteal serum progesterone level \< 3 ng/mL is indicative of chronic anovulation. For women who have been on ovarian suppressive therapy or other confounding medication (i.e. insulin sensitizing agents) within the last year prior to the study, a history of ≤8 menses per year prior to the initiation of this prior therapy will qualify as evidence of oligomenorrhea. For women with more regular bleeding patterns, but who are suspected to be experiencing anovulatory bleeding, a midluteal progesterone level \< 3ng/mL will be evidence of ovulatory dysfunction and qualify as anovulation. Undiagnosed persistent vaginal bleeding should be diagnosed and treated prior to enrollment. 2. Hyperandrogenism (either Hirsutism or Hyperandrogenemia) or Polycystic Ovaries on Ultrasound: 1. Hirsutism is determined by a modified Ferriman-Gallwey Score \>8 at screening exam (Hatch, Rosenfield et al. 1981 Aug 1). Subjects who have hirsutism do not need local or core labs documenting elevated androgen levels. 2. Hyperandrogenemia can be determined from local labs. Local cutoffs will be pre-determined by each site prior to study initiation. Hyperandrogenemia will be defined as an elevated total testosterone, or free androgen index (FAI)(in our lab at Penn State College of Medicine a total T \> 50 ng/dL or a free androgen index \>5) will allow entry into the study (Legro, Driscoll et al. 1998). The FAI is calculated from measurable values for total T and SHBG, as previously described (Miller, Rosner et al. 2004), using the following equation: (FAI = Total testosterone in nmol/L / SHBG in nmol/L) X 100. Outside lab values obtained within the last year documenting elevated T or FAI levels are sufficient to meet criteria of hyperandrogenemia. 3. Polycystic Ovaries on Ultrasound: We will use the revised Rotterdam criteria for diagnosing polycystic ovaries (Balen, Laven et al. 2003). PCO will be defined as either an ovary that contains 12 or more follicles measuring 2-9 mm in diameter, or an increased ovarian volume (\> 10 cm3) on one ovary for entry into the study. If there is a follicle \> 10 mm in diameter, the scan should be repeated at a time of ovarian quiescence in order to calculate volume and area if the subject does not otherwise qualify for the study. The presence of a single polycystic ovary (PCO), either by volume or morphology, is sufficient to provide the diagnosis.
Exclusion criteria
We will exclude subjects with medical conditions that represent contraindications to CC, aromatase inhibitors and/or pregnancy or who are unable to comply with the study procedures. We will exclude subjects with poorly controlled Type I or Type II diabetes; undiagnosed liver disease or dysfunction (based on serum liver enzyme testing); renal disease or abnormal serum renal function; significant anemia; history of deep venous thrombosis, pulmonary embolus, or cerebrovascular accident; uncontrolled hypertension, known symptomatic heart disease; history of or suspected cervical carcinoma, endometrial carcinoma, or breast carcinoma; undiagnosed vaginal bleeding, and use of other medications known to affect reproductive function or metabolism (e.g., OCP, GnRH agonists and antagonists, antiandrogens, gonadotropins, anti-obesity drugs, somatostatin, diazoxide, ACE inhibitors, and calcium channel blockers). As in PPCOS we will allow a 2 months washout period for subjects who desire to participate and discontinue exclusionary medications (most commonly OCP, but also possibly metformin), and a period of observation or treatment for correctable conditions. Couple Inclusion Criteria 1. Sperm concentration of 14 million/mL in at least one ejaculate within the last year, with at least some motile sperm. 2. Ability to have regular intercourse during the ovulation induction phase of the study. 3. At least one patent tube and normal uterine cavity as determined by sonohysterogram, hysterosalpingogram, or hysteroscopy/laparoscopy within the last 3 years. An uncomplicated intrauterine non-IVF pregnancy and uncomplicated delivery and postpartum course resulting in live birth within the last three years will also serve as sufficient evidence of a patent tube and normal uterine cavity as long as the subject did not have, during the pregnancy or subsequently, risk factors for Asherman's syndrome or tubal disease or other disorder leading to an increased suspicion for intrauterine abnormality or tubal occlusion. 4. No previous sterilization procedures (vasectomy, tubal ligation) that have been reversed. The prior procedure may affect study outcomes. Specific
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Live Birth | as few as 5 months, up to 16 months | The primary outcome measure is the occurrence of a live birth during the study period. Safety measures will be the number and type of reported adverse events in subjects and offspring. |
Secondary
| Measure | Time frame |
|---|---|
| Number of Pregnancy | as few as 5 months, up to 16 months |
| Number of Ovulations | as few as 5 months, up to 16 months |
| Number of Serious Adverse Events | as few as 5 months, up to 16 months |
| Neonatal Complication Rate | September 2008 - December 2011 |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Arm A: Clomiphene Citrate Clomiphene citrate 50 mg every day for 5 days (day 3-7 of cycle), for a total of 5 cycles or 20 weeks
Clomiphene citrate: Clomiphene citrate 50 mg every day for 5 days (day 3-7 of cycle), for a total of 5 cycles or 20 weeks | 376 |
| Arm B: Letrozole Letrozole 2.5 mg every day for 5 days (day 3-7 of cycle), for a total of 5 cycles or 20 weeks
Letrozole: Letrozole 2.5 mg every day for 5 days (day 3-7 of cycle), for a total of 5 cycles or 20 weeks | 374 |
| Total | 750 |
Baseline characteristics
| Characteristic | Arm A: Clomiphene Citrate | Arm B: Letrozole | Total |
|---|---|---|---|
| Age, Categorical <=18 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical >=65 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical Between 18 and 65 years | 376 Participants | 374 Participants | 750 Participants |
| Age, Continuous | 28.2 years STANDARD_DEVIATION 4 | 28.9 years STANDARD_DEVIATION 4.5 | 28.9 years STANDARD_DEVIATION 4.3 |
| Region of Enrollment United States | 376 Participants | 374 Participants | 750 Participants |
| Sex: Female, Male Female | 376 Participants | 374 Participants | 750 Participants |
| Sex: Female, Male Male | 0 Participants | 0 Participants | 0 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — |
| other Total, other adverse events | 283 / 355 | 285 / 359 |
| serious Total, serious adverse events | 13 / 376 | 21 / 374 |
Outcome results
Live Birth
The primary outcome measure is the occurrence of a live birth during the study period. Safety measures will be the number and type of reported adverse events in subjects and offspring.
Time frame: as few as 5 months, up to 16 months
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Arm A: Clomiphene Citrate | Live Birth | 72 Participants |
| Arm B: Letrozole | Live Birth | 103 Participants |
Neonatal Complication Rate
Time frame: September 2008 - December 2011
Population: Neonatal complications reported per infant, an infant could have more than one complication.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Arm A: Clomiphene Citrate | Neonatal Complication Rate | Neonatal hospitalization >3 days | 4 participants |
| Arm A: Clomiphene Citrate | Neonatal Complication Rate | Minor birth defect | 0 participants |
| Arm A: Clomiphene Citrate | Neonatal Complication Rate | Neonatal respiratory distress syndrome | 2 participants |
| Arm A: Clomiphene Citrate | Neonatal Complication Rate | Other complication | 4 participants |
| Arm A: Clomiphene Citrate | Neonatal Complication Rate | Intrauterine growth restriction | 1 participants |
| Arm A: Clomiphene Citrate | Neonatal Complication Rate | Congenital anomaly | 1 participants |
| Arm A: Clomiphene Citrate | Neonatal Complication Rate | Neonatal infectin | 2 participants |
| Arm A: Clomiphene Citrate | Neonatal Complication Rate | Neonatal death | 2 participants |
| Arm A: Clomiphene Citrate | Neonatal Complication Rate | Neonatal jaundice | 17 participants |
| Arm B: Letrozole | Neonatal Complication Rate | Neonatal death | 1 participants |
| Arm B: Letrozole | Neonatal Complication Rate | Neonatal jaundice | 27 participants |
| Arm B: Letrozole | Neonatal Complication Rate | Intrauterine growth restriction | 5 participants |
| Arm B: Letrozole | Neonatal Complication Rate | Neonatal respiratory distress syndrome | 7 participants |
| Arm B: Letrozole | Neonatal Complication Rate | Neonatal hospitalization >3 days | 4 participants |
| Arm B: Letrozole | Neonatal Complication Rate | Neonatal infectin | 2 participants |
| Arm B: Letrozole | Neonatal Complication Rate | Minor birth defect | 1 participants |
| Arm B: Letrozole | Neonatal Complication Rate | Other complication | 5 participants |
| Arm B: Letrozole | Neonatal Complication Rate | Congenital anomaly | 4 participants |
Number of Ovulations
Time frame: as few as 5 months, up to 16 months
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Arm A: Clomiphene Citrate | Number of Ovulations | 331 ovulations |
| Arm B: Letrozole | Number of Ovulations | 388 ovulations |
Number of Pregnancy
Time frame: as few as 5 months, up to 16 months
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Arm A: Clomiphene Citrate | Number of Pregnancy | 103 Participants |
| Arm B: Letrozole | Number of Pregnancy | 154 Participants |
Number of Serious Adverse Events
Time frame: as few as 5 months, up to 16 months
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Arm A: Clomiphene Citrate | Number of Serious Adverse Events | 13 events |
| Arm B: Letrozole | Number of Serious Adverse Events | 22 events |