- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01219491
Egg Donor Recipient Characteristics Preferences
March 4, 2013 updated by: Reproductive Medicine Associates of New Jersey
Do Egg Donor Recipient Characteristics Change Over Time?
To identify the characteristics in an egg donor that are important to a recipient and to see if those characteristics change over time.
Study Overview
Status
Completed
Conditions
Detailed Description
No study has explored how recipients' attitudes and reactions change over time regarding the selection criteria for their donors.
Consequently, programs have no guidance in how to counsel prospective recipients as to whether their donor preferences will change over time.
Participants will complete a survey at 4 points in time as they go through the process of selecting an egg donor and pursuing a pregnancy using that egg donor.
Study Type
Observational
Enrollment (Actual)
131
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Connecticut
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Norwalk, Connecticut, United States, 06850
- Reproductive Medicine Associates of Connecticut
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New Jersey
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Morristown, New Jersey, United States, 07960
- Reproductive Medicine Assoicates of New Jersey
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New York
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New York, New York, United States, 10022
- Reproductive Medicine Associates of New York
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
21 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients who are planning to undergo an egg donor cycle are eligible
Description
All patients planning to undergo an egg donor cycle are eligible- there are no specific inclusion or exclusion criteria beyond that.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
|---|
|
Egg donor recipients
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Characteristics of Donors
Time Frame: duration of study
|
To identify the characteristics of donors which are important to recipients and whether their importance changes over time.
|
duration of study
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Andrea M Braverman, PhD, Reproductive Medicine Associates of new Jersey
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
December 1, 2007
Primary Completion (Actual)
November 1, 2011
Study Completion (Actual)
November 1, 2011
Study Registration Dates
First Submitted
October 8, 2010
First Submitted That Met QC Criteria
October 8, 2010
First Posted (Estimate)
October 13, 2010
Study Record Updates
Last Update Posted (Estimate)
March 5, 2013
Last Update Submitted That Met QC Criteria
March 4, 2013
Last Verified
March 1, 2013
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- RMA-00-16
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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