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

NCT01513954 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 450

Last updated 2012-01-20

No results posted yet for this study

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.

Conditions

  • Infertility, Female

Sponsors & Collaborators

  • Watson Pharmaceuticals

    collaborator INDUSTRY

  • Red Rock Fertility Center

    lead OTHER

Principal Investigators

  • Eva D Littman, M.D. · Red Rock Fertility Center

Eligibility

Min Age
21 Years
Max Age
37 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-01-31
Primary Completion
2013-01-31
Completion
2013-06-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01513954 on ClinicalTrials.gov