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Retrospective Database Studies

This study has been completed.
Information provided by (Responsible Party):
Reproductive Medicine Associates of New Jersey Identifier:
First received: October 8, 2010
Last updated: November 16, 2015
Last verified: November 2015
Data collection and comparison of relationships between patient demographics, stimulation protocols and outcomes, retrieval and transfer outcomes, number and quality of oocytes and embryos retrieved and transferred, pregnancy rates and pregnancy outcomes.

All Patients Undergoing Infertility Treatment

Study Type: Observational
Official Title: Retrospective Database Studies From Reproductive Endocrinology Practice Looking at Relationships Between Demographics, Stimulation Protocols and Outcomes, Retrieval and Transfer Outcomes, Number and Quality of Oocytes and Embryos Retrieved and Transferred, Pregnancy Rates and Pregnancy Outcomes.

Resource links provided by NLM:

Further study details as provided by Reproductive Medicine Associates of New Jersey:

Primary Outcome Measures:
  • Improving Rates while Decreasing Adverse Outcomes [ Time Frame: duration of study ]
    Retrospective database analysis in order to advance the field of reproductive endocrinology, to learn about reproductive aging and diminished ovarian reserve, to correlate oocyte and embryo quality with pregnancy rates and outcomes, and to reduce adverse outcomes such as Ovarian Hyperstimulation Syndrome (OHSS) and multiple pregnancy rates.

Enrollment: 1
Study Start Date: June 2002
Study Completion Date: November 2015
Primary Completion Date: October 2015 (Final data collection date for primary outcome measure)
Detailed Description:
No patient treatment is associated with the study.

Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
All patients undergoing infertility treatment in our practice.

Inclusion Criteria:

Exclusion Criteria:

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT01219296

United States, New Jersey
Reproductive Medicine Associates of New Jersey
Basking Ridge, New Jersey, United States, 07920
Sponsors and Collaborators
Reproductive Medicine Associates of New Jersey
Principal Investigator: Richard T Scott, MD Reproductive Medicine Associates of New Jersey
  More Information

Additional Information:
Responsible Party: Reproductive Medicine Associates of New Jersey Identifier: NCT01219296     History of Changes
Other Study ID Numbers: RMA-00-01
Study First Received: October 8, 2010
Last Updated: November 16, 2015

Keywords provided by Reproductive Medicine Associates of New Jersey:

Additional relevant MeSH terms:
Genital Diseases, Male
Genital Diseases, Female processed this record on April 26, 2017