Ovulation Induction in Women With Clomiphene Citrate Resistant PCOS
Primary Purpose
Polycystic Ovary Syndrome, Infertility
Status
Completed
Phase
Early Phase 1
Locations
Egypt
Study Type
Interventional
Intervention
induction of ovulation using letrozole-pioglitazone-metformin
induction of ovulation using clomiphene citrate-pioglitazone-metformin
transvaginal ultrasound
body mass index (BMI) calculation
day 3: follicle stimulating hormone (FSH), luteinizing hormone (LH), thyroid stimulating hormone (TSH), total testosterone
pretreatment blood urea and serum creatinine
serum estradiol (E2) on day 12
serum progesterone on day 21
blood urea and serum creatinine every month
Sponsored by
About this trial
This is an interventional treatment trial for Polycystic Ovary Syndrome focused on measuring letrozole, clomiphene citrate, pioglitazone, metformin, ovulation induction, PCOS
Eligibility Criteria
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
Sites / Locations
- Cairo University
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
arm 1:letrozole-pioglitazone -metformin group
arm 2: clomiphene citrate-pioglitazone-metformin
Arm Description
Arm 1 will receive letrozole 2.5 mg/day starting from the 3rd day of the cycle and for 5 days and (combined pioglitazone 15 mg+ metformin 850 mg) once daily from the first day of the cycle for 10 days.
Arm 2 will receive clomiphene citrate 100 mg/day starting from the 3rd day of the cycle for 5 days and (combined pioglitazone 15 mg + metformin 850 mg) once daily from the first day of the cycle for 10 days.
Outcomes
Primary Outcome Measures
Ovulation Rate
Secondary Outcome Measures
Number of Follicles>18mm.
Endometrial Thickness
Pregnancy Rate
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01909141
Brief Title
Ovulation Induction in Women With Clomiphene Citrate Resistant PCOS
Official Title
Combined Letrozole-metformin-pioglitazone Versus Combined Clomiphene Citrate-metformin-pioglitazone in Clomiphene Citrate-resistant Women With Polycystic Ovary Syndrome
Study Type
Interventional
2. Study Status
Record Verification Date
September 2015
Overall Recruitment Status
Completed
Study Start Date
August 2013 (undefined)
Primary Completion Date
February 2014 (Actual)
Study Completion Date
April 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cairo University
4. Oversight
5. 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-pioglitazone with that of combined CC-metformin-pioglitazone in ovulation induction in CC-resistant PCOS women.
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 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Polycystic Ovary Syndrome, Infertility
Keywords
letrozole, clomiphene citrate, pioglitazone, metformin, ovulation induction, PCOS
7. Study Design
Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
100 (Actual)
8. Arms, Groups, and Interventions
Arm Title
arm 1:letrozole-pioglitazone -metformin group
Arm Type
Active Comparator
Arm Description
Arm 1 will receive letrozole 2.5 mg/day starting from the 3rd day of the cycle and for 5 days and (combined pioglitazone 15 mg+ metformin 850 mg) once daily from the first day of the cycle for 10 days.
Arm Title
arm 2: clomiphene citrate-pioglitazone-metformin
Arm Type
Active Comparator
Arm Description
Arm 2 will receive clomiphene citrate 100 mg/day starting from the 3rd day of the cycle for 5 days and (combined pioglitazone 15 mg + metformin 850 mg) once daily from the first day of the cycle for 10 days.
Intervention Type
Drug
Intervention Name(s)
induction of ovulation using letrozole-pioglitazone-metformin
Intervention Description
induction of ovulation will be done for arm 1 for 3 consecutive cycles unless pregnancy occured.
Intervention Type
Drug
Intervention Name(s)
induction of ovulation using clomiphene citrate-pioglitazone-metformin
Intervention Description
induction of ovulation for arm 2 will be done in 3 consecutive cycles unless pregnancy occured.
Intervention Type
Radiation
Intervention Name(s)
transvaginal ultrasound
Intervention Description
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
Intervention Type
Other
Intervention Name(s)
body mass index (BMI) calculation
Intervention Description
BMI will be calculated for all women by dividing the weight in kilograms by the height in meters squared
Intervention Type
Other
Intervention Name(s)
day 3: follicle stimulating hormone (FSH), luteinizing hormone (LH), thyroid stimulating hormone (TSH), total testosterone
Intervention Description
baseline hormonal assay (day 3 FSH, LH, TSH and total testosterone) will be done for all women.
Intervention Type
Other
Intervention Name(s)
pretreatment blood urea and serum creatinine
Intervention Description
blood urea and serum creatinine will be assayed before stating induction of ovulation to have baseline levels.
Intervention Type
Other
Intervention Name(s)
serum estradiol (E2) on day 12
Intervention Description
serum E2 will be assayed on day 12 of the cycle for all women.
Intervention Type
Other
Intervention Name(s)
serum progesterone on day 21
Intervention Description
serum progesterone will be assayed on day 21 for all women to monitor ovulation.
Intervention Type
Other
Intervention Name(s)
blood urea and serum creatinine every month
Intervention Description
blood urea and serum creatinine will be assayed every month during the treatment period to find out any hazards on kidney functions
Primary Outcome Measure Information:
Title
Ovulation Rate
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Number of Follicles>18mm.
Time Frame
3 months
Title
Endometrial Thickness
Time Frame
3 months
Title
Pregnancy Rate
Time Frame
3 months
Other Pre-specified Outcome Measures:
Title
Safety of Pioglitazone as Regards Serum Creatinine
Description
serum creatinine was measured at the end of the study period (after 3 months) in both groups.
Time Frame
3 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ghada Abdel Fattah Abdel Moety, lecturer
Organizational Affiliation
Cairo University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cairo University
City
Cairo
Country
Egypt
12. IPD Sharing Statement
Citations:
PubMed Identifier
26613820
Citation
El-khayat W, Abdel Moety G, Al Mohammady M, Hamed D. A randomized controlled trial of clomifene citrate, metformin, and pioglitazone versus letrozole, metformin, and pioglitazone for clomifene-citrate-resistant polycystic ovary syndrome. Int J Gynaecol Obstet. 2016 Feb;132(2):206-9. doi: 10.1016/j.ijgo.2015.06.063. Epub 2015 Nov 6.
Results Reference
derived
Learn more about this trial
Ovulation Induction in Women With Clomiphene Citrate Resistant PCOS
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