Luteal Support and Intrauterine Insemination (IUI) With Clomiphene Citrate

• Status: Completed
• Trial end date: 2012-07-01
• Target enrollment: 0
• Participant gender: Female

Summary

The purpose of this study is to assess the effect of luteal phase supplement (LPS) on pregnancy rate in IUI cycles stimulated with clomiphene citrate.

• Phase: N/A
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Universitair Ziekenhuis Brussel
• Treatments: Citric Acid; Clomiphene; Enclomiphene; Progesterone; Zuclomiphene

Criteria

Inclusion Criteria:

• Age ≤ 36 years

• Body mass index between 18 and 29

• Presence of both ovaries

• Basal levels of estradiol (≤ 80 pg/ml) and progesterone (≤ 1.6ng/ml) on day one of the cycle and a day three FSH level of <12IU/L

• Patients can enter the study only once.

• Only the first IUI attempt will be included ( at the 2nd and 3 rd attempt progesterone could be administrated if it is necessary but these attempts will be excluded from the study)

• Normal HSG (maximum 3 months prior starting the stimulation).

• Donor sperm can be included

Exclusion Criteria:

• Polycystic ovarian syndrome (Rotterdam criteria)

• Endometriosis(≥AFS III)