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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00682071
Other study ID # 2003-311
Secondary ID IRB# 2003-311 (U
Status Completed
Phase N/A
First received May 16, 2008
Last updated October 1, 2015
Start date August 2003
Est. completion date June 2007

Study information

Verified date May 2008
Source University of Wisconsin, Madison
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

Ultrasound (US) guided embryo transfer (ET) appears to improve pregnancy outcomes in IVF-ET. Most reports are done using a transabdominal (TAS) approach, in contrast to a transvaginal ultrasound (TVS) which does not require a full bladder. We sought to determine if either approach was better with respect to clinical outcomes.


Recruitment information / eligibility

Status Completed
Enrollment 224
Est. completion date June 2007
Est. primary completion date June 2007
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- All patients undergoing assisted reproductive cycles including autologous IVF, oocyte donation, and frozen embryo transfer (FET) cycles

Exclusion Criteria:

- Cases of severe ovarian hyper-stimulation requiring embryo cryopreservation and gestational surrogate cycles

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Wisconsin, Madison

Outcome

Type Measure Description Time frame Safety issue
Primary pregnancy rates for TAS and TVS ultrasound-guided ET groups August 2003 to June 2007 No
Secondary Length of time required for embryo transfer August 2003 to June 2007 No
Secondary differences between transferring physicians August 2003 to June 2007 No
Secondary multiple pregnancies August 2003 to June 2007 No
Secondary ectopic pregnancy rates August 2003 to June 2007 No
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