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Clinical Trials/NCT01137461
NCT01137461CompletedPhase 4

Evaluation of Efficacy of Embryo Transfer Procedure Guided by Transvaginal Ultrasound Versus Abdominal Ultrasound in Recipients of Oocytes. A Single-centre, Randomized Clinical Trial.

Fundació Privada Eugin2 sites in 1 country330 target enrollmentStarted: June 1, 2010Last updated:
Conditions

Trial Snapshot

Phase
Phase 4
Status
Completed
Sponsor
Enrollment
330
Locations
2
Primary Endpoint
Clinical pregnancy rate

Study Overview

Brief Summary

The objective of this study is to evaluate the efficacy of embryo transfer procedure guided by transvaginal ultrasound versus abdominal ultrasound in recipients of oocytes as well as the advantages and disadvantages of the new technique.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 50 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Oocyte recipients.
  • Uterus without previously detected anomalies.
  • Patients able to understand the study requirements who want to participate during all its duration and that have signed the informed consent.

Exclusion Criteria

  • Turner syndrome, Black race (significantly lower implantational rates)

Outcomes

Primary Outcomes

Clinical pregnancy rate

Time Frame: 40 days after embryo transfer

Evidence of gestational sac by transvaginal ultrasound

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Fundació Privada Eugin
Sponsor Class
Other

Study Sites (2)

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