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View Clinical Trial (Medical Research Study)


Examination of Serum Progesterone Levels in an IVF Population Following Two Types of Egg Aspiration

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City:   Las Vegas
State:   Nevada
Zip Code:   89148
Conditions:   Infertility, Female
Purpose:   The purpose of this study is to determine whether progesterone hormone levels differ following egg retrieval with a single lumen needle compared with a double lumen needle. These levels will be measured on several days before and after egg retrieval. The progesterone levels in each IVF group will also be compared to the group of women who are having IUI. In addition, these progesterone levels will be correlated with pregnancy outcomes.
Study Summary:   This is a prospective randomized trial consisting of 3 groups of patients. Following a long lupron protocol IVF cycle there is a need for supplemental progesterone. The purpose of this study is to determine what range of serum levels should be observed when differing methods of egg aspiration have been administered and whether or not there is a correlation with outcomes or pregnancies.
Criteria:   Inclusion Criteria: - Ages between 21-37 - Cycle Day 3 FSH between 2-12 - History of regular menstrual cycles between 24-34 days Exclusion Criteria: - Previous IVF failure - Severe male factor - Severe obesity, BMI > 40 - More than 20 follicles on ultrasound prior to retrieval
NCT ID:   NCT01513954
Primary Contact:   Principal Investigator
Eva D Littman, M.D.
Red Rock Fertility Center

Eva D Littman, M.D.
Phone: 702-262-0079
Email: drevalittman@hotmail.com
Backup Contact:   Email: charry@lasvegasfertility.com
Maria (Charry) R Lopez, M.D.
Phone: 702-262-0079
Location Contact:   Las Vegas, Nevada 89148
United States

Maria (Charry) R Lopez, MD
Phone: 702-262-0079
Email: charry@lasvegasfertility.com

Site Status: Recruiting

Data Source:   ClinicalTrials.gov
Date Processed:   May 24, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
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