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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00213148
Other study ID # 25550
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date March 10, 2005
Est. completion date December 12, 2007

Study information

Verified date September 2017
Source EMD Serono
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate and compare the safety and efficacy of various doses of the aromatase inhibitor (anastrozole) versus clomiphene citrate in stimulating follicular growth and ovulation in infertile women with ovulatory dysfunction.


Recruitment information / eligibility

Status Completed
Enrollment 271
Est. completion date December 12, 2007
Est. primary completion date December 12, 2007
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Aged 18-40 years

- Ovulatory dysfunction characterized by irregular and/or extended cycles

- Non-smoker

Exclusion Criteria:

- No previous gonadotropin treatment

- No more than 6 previous clomiphene treatment cycles

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Anastrozole 1 mg
Subjects will be administered orally with 1 mg of anastrozole once daily for 5 days in Cycle 1, 2 and 3 (each cycle = approximately 1 month).
Anastrozole 5 mg
Subjects will be administered orally with 5 mg of anastrozole once daily for 5 days in Cycle 1, 2 and 3 (each cycle = approximately 1 month).
Anastrozole 10 mg
Subjects will be administered orally with 10 mg of anastrozole once daily for 5 days in Cycle 1, 2 and 3 (each cycle = approximately 1 month).
Clomiphene Citrate 50 mg
Subjects will be administered orally with 50 mg of clomiphene citrate once daily for 5 days in Cycle 1, 2 and 3 (each cycle = approximately 1 month).
Clomiphene Citrate 100 mg
Subjects will be administered orally with 100 mg of clomiphene citrate once daily for 5 days in Cycle 2 and 3 (each cycle = approximately 1 month).

Locations

Country Name City State
United States Local US Medical Information Rockland Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
EMD Serono

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ovulation Rate in Cycle 1 Ovulation rate was defined as the percentage of subjects who ovulated (mid-luteal Progesteron [P4] level greater than or equal to [>=] 10 nanogram per milliliter [ng/mL] and/or pregnancy). Up to 1 month
Secondary Number of Subjects With Clinical Pregnancy in Cycle 1 Clinical pregnancy was defined as the existence of at least one ultrasonographically confirmed gestational sac in the uterus with fetal heart activity. Up to 1 month
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