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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00766714
Other study ID # UZGhent 002
Secondary ID
Status Completed
Phase N/A
First received October 3, 2008
Last updated October 3, 2008
Start date January 2000
Est. completion date December 2005

Study information

Verified date October 2008
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority Belgium: Institutional Review Board
Study type Interventional

Clinical Trial Summary

A prospective randomized trial comparing Cook K-SOFT-5100 and Frydman classical catheter 4.5 for embryo transfer in human IVF/ICSI was performed. Three experienced operators participated in the trial, using a fixed distance transfer protocol. Primary endpoint was clinical pregnancy rate, secondary endpoints were rates of difficult transfer and of catheter failure. Patients were randomized by a computer program immediately prior to embryo transfer.


Recruitment information / eligibility

Status Completed
Enrollment 1446
Est. completion date December 2005
Est. primary completion date December 2005
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patients undergoing embryo transfer in our IVF program between 2000 and 2005

Exclusion Criteria:

- patients not giving consent were excluded

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Device:
Cook K-SOFT-5100 catheter
A Cook K-SOFT-5100 catheter was used for embryo transfer in human IVF/ICSI
Frydman classical catheter
A Frydman classical catheter was used for embryo transfer in human IVF/ICSI

Locations

Country Name City State
Belgium University Hospital Ghent Ghent

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Ghent

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical pregnancy rates End of study No
Secondary Rates of difficult transfer End of study No
Secondary Catheter failure rate End of study No