Comparison of Crinone 8% Intravaginal Gel and IM Progesterone Supplementation for In Vitro Fertilization (IVF)

Completed · Phase 4

Conditions studied: Infertility

In brief

The goal of this research study is to compare the pregnancy rates for two different types of progesterone supplementation after in-vitro fertilization (IVF).

Key facts

Study ID

NCT00656201

Run by

Brigham and Women's Hospital

People needed

468

Starts

2003-07-01

Expected to finish

2009-07-01

Last updated by the study team

2011-09-22

Who can join

Age: 21 and older, up to 39. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Women of reproductive age (21-39) with infertility who are appropriate candidates for IVF/ET and have an FSH < 15 mIU/ml
• Women 21 to 39 years of age who have been assigned to stimulation of 2 to 8 amps of Luteal Lupron/FSH or Luteal Lupron FSH/HMG.

You may not qualify if…

• Women who have had more than 3 previous IVF/ET cycles

Where it is running

• Brigham and Women's Hospital — Boston, Massachusetts, United States

Full record on ClinicalTrials.gov

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