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NCT Number: NCT01909141

Ovulation Induction in Women With Clomiphene Citrate Resistant PCOS

Polycystic ovary syndrome (PCOS) affects 5-10% of women in childbearing age. Hyperinsulinemia contributes to chronic anovulation commonly encountered in women with PCOS. The first choice therapy is clomiphene citrate (CC). In CC resistant cases, the American College of Obstetrics and Gynecology (ACOG) recommends the use of insulin sensitizer metformin. Other insulin sensitizing agents include rosiglitazone and pioglitazone. Pioglitazone is said to improve fertility and ovulation in patients with PCOS.CC may be associated with poor endometrial thickening due to its antiestrogenic effect. Letrozole may improve this condition. In this study we will compare the effect of combined letrozole-metformin-pioglitazone with that of combined CC-metformin-pioglitazone in ovulation induction in CC-resistant PCOS women.

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Key information

About this study

Polycystic ovary syndrome (PCOS) affects 5-10% of women in childbearing age. Hyperinsulinemia contributes to chronic anovulation commonly encountered in women with PCOS. The first choice therapy is clomiphene citrate (CC). In CC resistant cases, the ACOG recommends the use of insulin sensitizer metformin. Other insulin sensitizing agents include rosiglitazone and pioglitazone. Pioglitazone is said to improve fertility and ovulation in patients with PCOS.CC has a long half-life (2 weeks), and this may have a negative effect on the cervical mucus and endometrium, leading to discrepancy between ovulation and conception rates. There has been a search for a compound capable of inducing ovulation but devoid of the adverse antiestrogenic effects of CC. recent studies have suggested that letrozole, an aromatase inhibitor, does not possess the adverse antiestrogenic effects of CC and is associated with higher pregnancy rates than CC treatment in patients with PCOS.

In this study we shall compare the effect of combined letrozole-metformin-pioglitazone with that of combined CC-metformin-pioglitazone in ovulation induction in CC-resistant PCOS women.This will be a prospective comparative clinical trial in which 2 groups of women will be generated (groups A and B) using the sealed envelopes randomization method.Group A (40 women) will receive: letrozole 2.5 mg/day from 3rd day of the cycle for 5 days and (pioglitazone 15 mg + metformin 850 mg) once daily from 1st day of the cycle for 10 days. Group B (40 women) will receive clomiphene citrate 100 mg/day from 3rd day of the cycle for 5 days and (pioglitazone 15 mg + metformin 850 mg) once daily from 1st day of the cycle for 10 days. Ovulation will be monitored by vaginal ultrasound and serum estrogen and progesterone.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • 20-40 years old
  • PCOS infertile women resistant to CC for3 cycles

Exclusion criteria

  • presence of medical disorders as diabetes, hypertension, cardiac problems, liver or kidney diseases, hyperprolactinemia or thyroid dysfunction.
  • use of gonadotropins before
  • previous ovarian drilling
  • presence of urinary symptoms especially bloody urine

Treatment and study plan

induction of ovulation using letrozole-pioglitazone-metformin

Drug

induction of ovulation will be done for arm 1 for 3 consecutive cycles unless pregnancy occured.

induction of ovulation using clomiphene citrate-pioglitazone-metformin

Drug

induction of ovulation for arm 2 will be done in 3 consecutive cycles unless pregnancy occured.

Transvaginal ultrasound

Radiation

transvaginal ultrasound will be done starting from day 10 and every 48 hours until finding a follicle of > 18 mm or till day 20 of the cycle

body mass index (BMI) calculation

Other

BMI will be calculated for all women by dividing the weight in kilograms by the height in meters squared

day 3: follicle stimulating hormone (FSH), luteinizing hormone (LH), thyroid stimulating hormone (TSH), total testosterone

Other

baseline hormonal assay (day 3 FSH, LH, TSH and total testosterone) will be done for all women.

pretreatment blood urea and serum creatinine

Other

blood urea and serum creatinine will be assayed before stating induction of ovulation to have baseline levels.

serum estradiol (E2) on day 12

Other

serum E2 will be assayed on day 12 of the cycle for all women.

serum progesterone on day 21

Other

serum progesterone will be assayed on day 21 for all women to monitor ovulation.

blood urea and serum creatinine every month

Other

blood urea and serum creatinine will be assayed every month during the treatment period to find out any hazards on kidney functions

Primary outcomes

  1. Ovulation Rate

    Time frame: 3 months

Secondary outcomes

  1. Number of Follicles>18mm.

    Time frame: 3 months

  2. Endometrial Thickness

    Time frame: 3 months

  3. Pregnancy Rate

    Time frame: 3 months

Other outcomes

  1. Safety of Pioglitazone as Regards Serum Creatinine

    Time frame: 3 months

    serum creatinine was measured at the end of the study period (after 3 months) in both groups.

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Official study title

Combined Letrozole-metformin-pioglitazone Versus Combined Clomiphene Citrate-metformin-pioglitazone in Clomiphene Citrate-resistant Women With Polycystic Ovary Syndrome

Important dates

Study start
2013
Primary completion
2014
Study completion
2014
First posted
Jul 26, 2013
Registry last updated
Oct 20, 2015

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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