Ovulation Induction in Clomiphene Citrate Resistant PCO Women

Sponsor
Cairo University (Other)
Overall Status
Completed
CT.gov ID
NCT02341703
Collaborator
(none)
100
1
2
4.9
20.3

Study Details

Study Description

Brief Summary

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 with that of combined letrozole-pioglitazone in ovulation induction in CC-resistant PCOS women

Condition or Disease Intervention/Treatment Phase
Early Phase 1

Detailed Description

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 the investigators shall compare the effect of combined letrozole-metformin with that of combined letrozole-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 (50 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 (50 women) will receive letrozole 2.5 mg/day from 3rd day of the cycle for 5 days and metformin 500 mg three times daily from continuously untill pregncy occurrs. Ovulation will be monitored by vaginal ultrasound and serum estrogen and progesterone.

Study Design

Study Type:
Interventional
Actual Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Letrozole-metformin Versus Letrozole-metformin-pioglitazone in PCO Clomiphene Citrate Resistant Women
Study Start Date :
Feb 1, 2015
Actual Primary Completion Date :
Jul 1, 2015
Actual Study Completion Date :
Jul 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: letrozole-metformin group

this group will receive letrozole 2.5 mg daily from day 3 of the cycle and for 5 days + metformin 500 mg three times daily from the first day of the cycle and continuous for three months unless pregnancy occurred. treatment will continue for 3 cycles unless pregnancy occurred. for this group: transvaginal ultrasound will monitor follicular enlargement laboratory investigations in the form of day 3 FSH, LH, TSH and serum testosterone will be done day 12 E2 day 21 serum progesterone

Drug: letrozole-metformin
letrozole 2.5 mg will be given daily from day 3 of the cycle for 5 days + metformin 500 mg three times daily continuously for 3 months unless pregnancy occurred
Other Names:
  • femara-cidophage
  • Radiation: transvaginal ultrasound
    transvaginal ultrasound will be done from day 10 of the cycle and every other day for monitoring of follicular enlargement.

    Other: laboratory investigations
    day 3: FSH, LH, TSH, and total testosterone day 12 serum E2 day 21 serum progesterone

    Active Comparator: letrozole-metformin-pioglitazone group

    this group will receive letrozole 2.5 mg daily from day 3 of the cycle and for 5 days + (metformin 850 mg + pioglitazone 15 mg) once daily from the first day of the cycle and for 10 days. treatment will continue for 3 cycles unless pregnancy occurred. for this group: transvaginal ultrasound will monitor follicular enlargement laboratory investigations in the form of day 3 FSH, LH, TSH and serum testosterone will be done day 12 E2 day 21 serum progesterone

    Drug: letrozole-metformin-pioglitazone
    letrozole will be given daily from day 3 of the cycle for 5 days + (metformin 850 mg + pioglitazone 15 mg) from the first day of the cycle for 10 days.
    Other Names:
  • femara- bioglita plus
  • Radiation: transvaginal ultrasound
    transvaginal ultrasound will be done from day 10 of the cycle and every other day for monitoring of follicular enlargement.

    Other: laboratory investigations
    day 3: FSH, LH, TSH, and total testosterone day 12 serum E2 day 21 serum progesterone

    Outcome Measures

    Primary Outcome Measures

    1. ovulation rate [6 months]

    Secondary Outcome Measures

    1. pregnancy rate [6 months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 40 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • 20-40 years old

    • PCOS infertile women resistant to CC for 3 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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 faculty of medicine, Cairo University Cairo Egypt 002

    Sponsors and Collaborators

    • Cairo University

    Investigators

    • Principal Investigator: Ghada Abdel Fattah Abdel Moety, lecturer, Cairo University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ghada Abdel Fattah, assistant professor of Obstetrics and Gynecology, Cairo University
    ClinicalTrials.gov Identifier:
    NCT02341703
    Other Study ID Numbers:
    • University Hospital
    First Posted:
    Jan 19, 2015
    Last Update Posted:
    Jul 28, 2015
    Last Verified:
    Jul 1, 2015

    Study Results

    No Results Posted as of Jul 28, 2015