anovulation postcoital test
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - WHO class II anovulatory women who ovulate following use of incremental CC doses from 50-150 mg starting on day 3-5 during 5 days of the cycle. - normal serum prolactin (0,05 - 0,80 IU/l, and TSH (0,4-4,0 mU/l - age 18 years or older - total motial sperm count above 1 million, according the modified criteria of the WHO
Exclusion criteria
Exclusion criteria: - anovulatory on CC 150 mg / day - known bilateral tubel pathology
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pregnancy rates in women with a positive compared to pregnancy rates in women with a negative postcoital test within a time horizon of six months | — |
Secondary
| Measure | Time frame |
|---|---|
| • Positive pregnancy test • occurrence of ovulation • total number of postcoital tests performed • median time to pregnancy in the two groups. • clinical pregnancy, defined as any registerd heart beath at sonography • miscarriage, defined as loss of an intra uterine pregnancy (confirmed by ultrasound or histologic examination) before the 20th week of pregnancy. • multiple pregnancy, defined as a registered heart beath of at least two fetuses at 12 weeks of gestation • costs | — |
Countries
Netherlands