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Clinical Trials/NCT01513954
NCT01513954
Unknown
Not Applicable

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

Red Rock Fertility Center1 site in 1 country450 target enrollmentStarted: January 2012Last updated:

Overview

Phase
Not Applicable
Sponsor
Red Rock Fertility Center
Enrollment
450
Locations
1

Overview

Brief Summary

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.

Detailed Description

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.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Prospective

Eligibility Criteria

Ages
21 Years to 37 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

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

Investigators

Sponsor
Red Rock Fertility Center
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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