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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01805505
Other study ID # MAD-EH-01-2012-01
Secondary ID
Status Terminated
Phase Early Phase 1
First received March 1, 2013
Last updated March 5, 2017
Start date February 2012
Est. completion date December 2016

Study information

Verified date March 2017
Source IVI Madrid
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Transabdominal ultrasound guidance is the golden standard for embryo transfers. Transvaginal ultrasound guidance was proposed recently to provide better visualization and reduce patient discomfort as embryo transfer can be performed with an empty bladder in this case. The purpose of this study is to determine whether there are any differences between transvaginal and transabdominal ultrasound-guided embryo transfer in terms of ease of use, patient satisfaction, and treatment outcome.


Recruitment information / eligibility

Status Terminated
Enrollment 346
Est. completion date December 2016
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 49 Years
Eligibility Inclusion Criteria:

- Patients undergoing oocyte donation treatment with transfer of 2 embryos on day 3

Exclusion Criteria:

- Submucous or >3 cm intramural fibroids

- Turner syndrome

- Black recipients

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Transvaginal ultrasound-guided embryo transfer
Embryo transfer of two day-3 embryos performed with the Kitazato Long ET catheter (Kitazato Medical Co. Ltd., Tokyo, Japan), guided by transvaginal ultrasound
Transabdominal ultrasound-guided embryo transfer
Embryo transfer of two day-3 embryos performed with the Cook Soft-Trans ET catheter (Cook Medical Inc., Bloomington, IN, USA), guided by transabdominal ultrasound

Locations

Country Name City State
Spain IVI Madrid Madrid

Sponsors (1)

Lead Sponsor Collaborator
IVI Madrid

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pregnancy rate Proportion of patients with a positive pregnancy test At performing the pregnancy test 11 days post-embryo transfer
Secondary Clinical pregnancy rate Proportion of patients with at least one gestational sac at first pregnancy ultrasound At first pregnancy ultrasound (3 weeks post-embryo transfer)
Secondary Ongoing pregnancy rate Proportion of patients with at least one live intrauterine fetus at 10 weeks post-embryo transfer At 10 weeks post-embryo transfer
Secondary Menstruation-like pain Measured on a three-level scale (none/mild/strong) At embryo transfer
Secondary Discomfort related to vesical distension Measured on a three-level scale (none/mild/strong) At embryo transfer
Secondary Overall discomfort Measured on a three-level scale (none/mild/strong) At embryo transfer
Secondary Difficulty using the assigned technique faced by operators Measured on a three-level scale (easy/moderately difficult/very difficult) At embryo transfer
Secondary Catheterization time At embryo transfer
Secondary Conversion to the opposite technique Proportion of cases in which embryo transfer was performed using the technique of the opposite randomization arm (i.e., proportion of patients randomized to have transabdominal ultrasound-guided transfer in whom transvaginal ultrasound-guided was performed, and the other way around) At embryo transfer
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