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Clinical Trials/NCT00824629
NCT00824629CompletedNot Applicable

Direct Transfer vs Previous Cervical Canalization Transfer ("Afterloading"): Randomized Clinical Trial.

Institut Universitari Dexeus2 sites in 1 country400 target enrollmentStarted: October 1, 2008Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
400
Locations
2
Primary Endpoint
Clinical pregnancy

Study Overview

Brief Summary

The purpose of this study is to evaluate two types of embryo transfer procedure.

The investigators will compare direct embryo transfer against afterloading embryo transfer.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
18 Years to 42 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients in IVF/CICSI program
  • Transfer day:2 or 3 after ovum pick-up

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Clinical pregnancy

Time Frame: 8 weeks after embryo transfer

Secondary Outcomes

  • Duration of embryo transfer(During embryo transfer procedure)
  • Difficulty of embryo transfer(During embryo transfer procedure)

Investigators

Sponsor
Institut Universitari Dexeus
Sponsor Class
Other

Study Sites (2)

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