NCT01219530

Brief Summary

To explore the attitudes and reactions of gestational carriers and intended parents though their medical, pregnancy and postpartum experiences.

Trial Health

30
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Timeline
Completed

Started Apr 2010

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
withdrawn

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2010

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

October 8, 2010

Completed
5 days until next milestone

First Posted

Study publicly available on registry

October 13, 2010

Completed
5.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2015

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2016

Completed
Last Updated

January 23, 2013

Status Verified

January 1, 2013

Enrollment Period

5.7 years

First QC Date

October 8, 2010

Last Update Submit

January 22, 2013

Conditions

AttitudesReactionsPsychopathology

Keywords

gestational carrierintended parent

Study Arms (2)

Gestational Carriers

Intended Parents

Eligibility Criteria

Age21 Years - 60 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Patients participating in the gestational carrier program, either as a gestation carrier or an intended parent.

None, other than being either a gestational carrier or intended parent.

Contact the study team to discuss eligibility requirements. They can help determine if this study is right for you.

Sponsors & Collaborators

Study Sites (1)

Reproductive Medicine Associates of New Jersey

Morristown, New Jersey, 07960, United States

Location

MeSH Terms

Conditions

Behavior

Study Officials

  • Andrea M Braverman, PhD

    Reproductive Medicine Associates of New Jersey

    PRINCIPAL INVESTIGATOR
0

Study Design

Study Type
observational
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 8, 2010

First Posted

October 13, 2010

Study Start

April 1, 2010

Primary Completion

December 1, 2015

Study Completion

December 1, 2016

Last Updated

January 23, 2013

Record last verified: 2013-01

Locations

US(1)