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Luteal Support and Intrauterine Insemination (IUI) With Clomiphene Citrate

Information source: Universitair Ziekenhuis Brussel
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Infertility

Intervention: micronized progesterone (Drug)

Phase: N/A

Status: Completed

Sponsored by: Universitair Ziekenhuis Brussel

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.

Clinical Details

Official title: Ovulation Induction With Clomiphene Citrate: to Support or Not to Support the Luteal Phase

Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Primary outcome: ongoing pregnancy rate

Secondary outcome: implantation rate,clinical pregnancy rate

Eligibility

Minimum age: 18 Years. Maximum age: 36 Years. Gender(s): Female.

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)

Locations and Contacts

Additional Information

Starting date: September 2008
Last updated: July 1, 2013

Page last updated: August 23, 2015

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