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Retrospective Database Studies

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01219296
First Posted: October 13, 2010
Last Update Posted: November 17, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Reproductive Medicine Associates of New Jersey
  Purpose
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.

Condition
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.
  Eligibility

Information from the National Library of Medicine

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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.
Criteria

Inclusion Criteria:

Exclusion Criteria:

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01219296


Locations
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
Investigators
Principal Investigator: Richard T Scott, MD Reproductive Medicine Associates of New Jersey
  More Information

Additional Information:
Responsible Party: Reproductive Medicine Associates of New Jersey
ClinicalTrials.gov Identifier: NCT01219296     History of Changes
Other Study ID Numbers: RMA-00-01
First Submitted: October 8, 2010
First Posted: October 13, 2010
Last Update Posted: November 17, 2015
Last Verified: November 2015

Keywords provided by Reproductive Medicine Associates of New Jersey:
infertility
IVF

Additional relevant MeSH terms:
Infertility
Genital Diseases, Male
Genital Diseases, Female