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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01219296
Other study ID # RMA-00-01
Secondary ID
Status Completed
Phase N/A
First received October 8, 2010
Last updated November 16, 2015
Start date June 2002
Est. completion date November 2015

Study information

Verified date November 2015
Source Reproductive Medicine Associates of New Jersey
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

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.


Description:

No patient treatment is associated with the study.


Recruitment information / eligibility

Status Completed
Enrollment 1
Est. completion date November 2015
Est. primary completion date October 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

Exclusion Criteria:

Study Design

N/A


Related Conditions & MeSH terms

  • All Patients Undergoing Infertility Treatment
  • Infertility

Locations

Country Name City State
United States Reproductive Medicine Associates of New Jersey Basking Ridge New Jersey

Sponsors (1)

Lead Sponsor Collaborator
Reproductive Medicine Associates of New Jersey

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Improving Rates while Decreasing Adverse Outcomes 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. duration of study No