subfertility
Conditions
Interventions
Couples were randomly allocated to IUI for six months or expectant management for six months. In the first three IUI cycles no controlled ovarian hyperstimulation (COH) was given. If these attempts fa
Sponsors
OFO-project
t.a.v. B.W. Mol
Academic Medical Center
Center of Reporductive medicine, H4-213
Postbus 22660
1100 DD Amsterdam
Phone: 0031205663857
Fax: 0031206963489
e-mail: ofoproject@amc.uva.nl or b.mol1@chello.nl
Eligibility
Inclusion criteria
Inclusion criteria: Couples with a cervical factor and otherwise no factors that reduced their fertility, i.e. a prognosis for a treatment independent ongoing pregnancy in the next year higher than 30%. A cervical factor was diagnosed by a well-timed, non-progressive post-coital test (PCT) with normal semen parameters.
Exclusion criteria
Exclusion criteria: All other subfertile couples.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint was ongoing pregnancy within six months. Ongoing pregnancy was defined as the presence of foetal cardiac activity at transvaginal sonography at a gestational age of at least 12 weeks. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints were total number of clinical pregnancies, miscarriages and multiple pregnancies. | — |
Contacts
Public ContactP. Steures
Academic Medical Center (AMC), Center of Reproductive medicine, OFO-project, H4-213, P.O. Box 22660
Outcome results
None listed