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Pregnancy in Polycystic Ovary Syndrome II

A 20 Week Double-Blind Randomized Trial of Clomiphene Citrate and Letrozole for the Treatment of Infertility in Women With Polycystic Ovary Syndrome

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00719186
Acronym
PPCOSII
Enrollment
750
Registered
2008-07-21
Start date
2009-02-28
Completion date
2013-05-31
Last updated
2018-06-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Polycystic Ovary Syndrome, Pregnancy

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

DRUGClomiphene citrate

Clomiphene citrate 50 mg every day for 5 days (day 3-7 of cycle), for a total of 5 cycles or 20 weeks

DRUGLetrozole

Letrozole 2.5 mg every day for 5 days (day 3-7 of cycle), for a total of 5 cycles or 20 weeks

Sponsors

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
CollaboratorNIH
Penn State University
CollaboratorOTHER
University of Colorado, Denver
CollaboratorOTHER
University of Michigan
CollaboratorOTHER
University of Pennsylvania
CollaboratorOTHER
The University of Texas Health Science Center at San Antonio
CollaboratorOTHER
University of Vermont
CollaboratorOTHER
Wayne State University
CollaboratorOTHER
Yale University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

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

MeasureTime frameDescription
Live Birthas few as 5 months, up to 16 monthsThe 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

MeasureTime frame
Number of Pregnancyas few as 5 months, up to 16 months
Number of Ovulationsas few as 5 months, up to 16 months
Number of Serious Adverse Eventsas few as 5 months, up to 16 months
Neonatal Complication RateSeptember 2008 - December 2011

Countries

United States

Participant flow

Participants by arm

ArmCount
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
Total750

Baseline characteristics

CharacteristicArm A: Clomiphene CitrateArm B: LetrozoleTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
376 Participants374 Participants750 Participants
Age, Continuous28.2 years
STANDARD_DEVIATION 4
28.9 years
STANDARD_DEVIATION 4.5
28.9 years
STANDARD_DEVIATION 4.3
Region of Enrollment
United States
376 Participants374 Participants750 Participants
Sex: Female, Male
Female
376 Participants374 Participants750 Participants
Sex: Female, Male
Male
0 Participants0 Participants0 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
283 / 355285 / 359
serious
Total, serious adverse events
13 / 37621 / 374

Outcome results

Primary

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

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Arm A: Clomiphene CitrateLive Birth72 Participants
Arm B: LetrozoleLive Birth103 Participants
p-value: 0.007Chi-squared
Secondary

Neonatal Complication Rate

Time frame: September 2008 - December 2011

Population: Neonatal complications reported per infant, an infant could have more than one complication.

ArmMeasureGroupValue (NUMBER)
Arm A: Clomiphene CitrateNeonatal Complication RateNeonatal hospitalization >3 days4 participants
Arm A: Clomiphene CitrateNeonatal Complication RateMinor birth defect0 participants
Arm A: Clomiphene CitrateNeonatal Complication RateNeonatal respiratory distress syndrome2 participants
Arm A: Clomiphene CitrateNeonatal Complication RateOther complication4 participants
Arm A: Clomiphene CitrateNeonatal Complication RateIntrauterine growth restriction1 participants
Arm A: Clomiphene CitrateNeonatal Complication RateCongenital anomaly1 participants
Arm A: Clomiphene CitrateNeonatal Complication RateNeonatal infectin2 participants
Arm A: Clomiphene CitrateNeonatal Complication RateNeonatal death2 participants
Arm A: Clomiphene CitrateNeonatal Complication RateNeonatal jaundice17 participants
Arm B: LetrozoleNeonatal Complication RateNeonatal death1 participants
Arm B: LetrozoleNeonatal Complication RateNeonatal jaundice27 participants
Arm B: LetrozoleNeonatal Complication RateIntrauterine growth restriction5 participants
Arm B: LetrozoleNeonatal Complication RateNeonatal respiratory distress syndrome7 participants
Arm B: LetrozoleNeonatal Complication RateNeonatal hospitalization >3 days4 participants
Arm B: LetrozoleNeonatal Complication RateNeonatal infectin2 participants
Arm B: LetrozoleNeonatal Complication RateMinor birth defect1 participants
Arm B: LetrozoleNeonatal Complication RateOther complication5 participants
Arm B: LetrozoleNeonatal Complication RateCongenital anomaly4 participants
Secondary

Number of Ovulations

Time frame: as few as 5 months, up to 16 months

ArmMeasureValue (NUMBER)
Arm A: Clomiphene CitrateNumber of Ovulations331 ovulations
Arm B: LetrozoleNumber of Ovulations388 ovulations
Secondary

Number of Pregnancy

Time frame: as few as 5 months, up to 16 months

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Arm A: Clomiphene CitrateNumber of Pregnancy103 Participants
Arm B: LetrozoleNumber of Pregnancy154 Participants
Secondary

Number of Serious Adverse Events

Time frame: as few as 5 months, up to 16 months

ArmMeasureValue (NUMBER)
Arm A: Clomiphene CitrateNumber of Serious Adverse Events13 events
Arm B: LetrozoleNumber of Serious Adverse Events22 events

Source: ClinicalTrials.gov · Data processed: May 23, 2026