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Completed

NCT Number: NCT02802865

Combined Letrozole and Clomid in Women With Infertility and PCOS

This study evaluates the addition of clomid to letrozole for the treatment of infertility in women with polycystic ovary syndrome. Half of the participants will receive letrozole and clomid in combination, while the other half will receive letrozole alone.

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Key information

Age range

18 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 4

Primary location

University of Iowa Hospitals & Clinics

Iowa City, Iowa, 52242, United States

About this study

Letrozole and Clomid are both used for ovulation induction, but they have different mechanisms of action. Letrozole has been shown to be superior to clomid in achieving live birth rates in women with infertility and polycystic ovary syndrome. However, the combination of these medications has not been studied. This is a pilot study to evaluate if the combination treatment has improved efficacy as measured by ovulation rate.

This is a randomized controlled trial of letrozole versus letrozole and clomiphene citrate (CC) for one menstrual cycle. Women will be randomized in a 1:1 ratio to receive letrozole 2.5 mg or combination of letrozole 2.5 mg and clomiphene 50 mg for 5 days on days 3-7 of menstrual cycle. The women and their partners will be instructed to have regular intercourse with the intent to conceive during the cycle. Patients will have an transvaginal ultrasound mid cycle and to evaluate number of follicles (>15 mm), follicle size, endometrial thickness and pattern. Patients will have mid- luteal phase progesterone level drawn to evaluate ovulation. Side effect profile will also be monitored.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Willing to comply with all study procedures and be available for the duration of the study
  • Diagnosis of infertility: Inability of couple to achieve successful pregnancy after 12 months of regular timed unprotected intercourse in women less than 35 years of age; and after 6 months of regular intercourse without use of contraception in women 35 years and older
  • Diagnosis of polycystic ovary syndrome based on Revised Rotterdam criteria
  • Ability to have regular intercourse during the ovulation induction phase of the study
  • Normal sperm concentration of 15 million/mL and with normal motility of > 40% according to World Health Organization cutoff points, in at least one ejaculate during the previous year

Exclusion criteria

  • Current pregnancy
  • Current use of hormonal contraception; use of any type of combined contraceptive or oral progestins within the past month; or use of hormonal implants or depo progestins within the past 3 months
  • Other known cause of infertility: endometriosis, tubal factor, uterine abnormalities
  • Uncorrected thyroid disease
  • Untreated hyperprolactinemia.
  • Medical conditions in which avoiding pregnancy is recommended until under improved control: poorly controlled Type 1 or Type 2 diabetes, poorly controlled hypertension
  • Contraindications to clomiphene citrate: hypersensitivity to CC or any of its components, history of liver disease or known liver disease, unknown cause of abnormal uterine bleeding, or intracranial lesion
  • Contraindications to letrozole: hypersensitivity to letrozole or any of its components.
  • Use of medications known to affect reproductive function or metabolism or that are an absolute contraindication during pregnancy within the past month.
  • If patients are suspected based on clinical findings for other etiologies that mimic PCOS, work up must be completed to exclude other etiologies prior to enrollment (i.e. Cushing's syndrome, androgen-secreting tumor).

Treatment and study plan

Clomiphene

Drug

Other names: clomid, clomiphene citrate

letrozole

Drug

Other names: femara

Primary outcomes

  1. Number of Participants Achieving Ovulation Measured by Mid-luteal Progesterone Level

    Time frame: 7 days following LH surge or at cycle day 21 if no LH surge was detected

    Ovulation: mid-luteal progesterone > /=3 ng/mL. No ovulation: mid-luteal progesterone <3ng/mL.

Secondary outcomes

  1. Number of Developing Follicles

    Time frame: Cycle day 12-14

    Number of follicles measuring > 10mm on ultrasound

  2. Size of Largest Developing Follicle

    Time frame: Cycle day 12-14

    Size of largest follicle on ultrasound

  3. Endometrial Thickness

    Time frame: Cycle day 12-14

    Thickness of endometrial lining assessed by ultrasound

  4. Conception

    Time frame: 5 weeks after treatment

    Conception: a positive serum or urinary test of hCG; No conception: Neither a positive serum or urinary test of hCG

  5. Clinical Pregnancy

    Time frame: 6-7 weeks after treatment

    Clinical Pregnancy: an intrauterine pregnancy with fetal heart motion determined by ultrasonography; No Clinical Pregnancy: no intrauterine pregnancy with fetal heart motion determined by ultrasonography

  6. Multiple Gestation

    Time frame: 9-10 months after treatment

    Multiple Gestation: an intrauterine pregnancy with multiple fetal heart rates determined by ultrasonography; No Multiple Gestation: either no intrauterine pregnancy, or an intrauterine pregnancy with a single fetal heart rate determined by ultrasonography

  7. Live Birth

    Time frame: 9-10 months after treatment

    Live Birth: delivery of a live infant; No Live Birth: no delivery of a live infant

  8. Pregnancy Loss

    Time frame: 9-10 months after treatment

    Pregnancy Loss: any pregnancy loss including biochemical pregnancy, ectopic pregnancy, and miscarriage; No Pregnancy Loss: no pregnancy loss including biochemical pregnancy, ectopic pregnancy, or miscarriage.

Sponsors and collaborators

Lead sponsor

Rachel Mejia

Other

Registry information

Official study title

Combined Letrozole and Clomid in Polycystic Ovary Syndrome: a Randomized Control Trial of Combination of Letrozole and Clomiphene Citrate or Letrozole Alone for the Treatment of Infertility in Women With Polycystic Ovary Syndrome

Important dates

Study start
2016
Primary completion
2018
Study completion
2019
First posted
Jun 16, 2016
Registry last updated
Sep 27, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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