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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
October 8, 2010
October 13, 2010
November 17, 2015
June 2002
October 2015   (Final data collection date for primary outcome measure)
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.
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Complete list of historical versions of study NCT01219296 on ClinicalTrials.gov Archive Site
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Retrospective Database Studies
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.
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.
No patient treatment is associated with the study.
Observational
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Non-Probability Sample
All patients undergoing infertility treatment in our practice.
All Patients Undergoing Infertility Treatment
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
1
November 2015
October 2015   (Final data collection date for primary outcome measure)

Inclusion Criteria:

Exclusion Criteria:

Sexes Eligible for Study: All
18 Years to 65 Years   (Adult)
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT01219296
RMA-00-01
No
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Reproductive Medicine Associates of New Jersey
Reproductive Medicine Associates of New Jersey
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Principal Investigator: Richard T Scott, MD Reproductive Medicine Associates of New Jersey
Reproductive Medicine Associates of New Jersey
November 2015