Single Embryo Transfer Versus Double Embryo Transfer

NCT ID: NCT00814398

Last Updated: 2016-01-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

199 participants

Study Classification

INTERVENTIONAL

Study Start Date

2008-12-31

Study Completion Date

2009-09-30

Brief Summary

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The aim of this project is to study the best number (1 or 2)and day (3 vs 5)of embryo transfer in good prognosis patient.

Detailed Description

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Conditions

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Infertility

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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SET on day 3

Single embryo transfer on day 3 of embryo development

Group Type EXPERIMENTAL

Single Embryo Transfer (SET)

Intervention Type PROCEDURE

A single embryo is transferred during an IVF treatment

DET on day 3

Double embryo transfer on day 3 of embryo development

Group Type EXPERIMENTAL

Double Embryo Transfer (DET)

Intervention Type PROCEDURE

Two embryos are transferred during an IVF treatment

SET on day 5

Single embryo transfer on day 5 of embryo development

Group Type EXPERIMENTAL

Single Embryo Transfer (SET)

Intervention Type PROCEDURE

A single embryo is transferred during an IVF treatment

DET on day 5

Double embryo transfer on day 5 of embryo development

Group Type EXPERIMENTAL

Double Embryo Transfer (DET)

Intervention Type PROCEDURE

Two embryos are transferred during an IVF treatment

Interventions

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Double Embryo Transfer (DET)

Two embryos are transferred during an IVF treatment

Intervention Type PROCEDURE

Single Embryo Transfer (SET)

A single embryo is transferred during an IVF treatment

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Good prognosis IVF patients

Exclusion Criteria

* Bad prognosis IVF patients
Minimum Eligible Age

18 Years

Maximum Eligible Age

37 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Vida Recoletas Sevilla

OTHER

Sponsor Role lead

Responsible Party

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Manuel Fernandez-Sanchez

Primary Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Manuel Fernandez, MD

Role: PRINCIPAL_INVESTIGATOR

Vida Recoletas Sevilla

Locations

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IVI-Sevilla

Seville, , Spain

Site Status

Countries

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Spain

Other Identifiers

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IVISEV-002SET

Identifier Type: -

Identifier Source: org_study_id

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